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研究生: 阮林如梅
Nguyen, Lam Nhu Mai
論文名稱: 栓菌屬真菌子實體萃取物的化學成分研究
Chemical Constituents from the Fungi Fruiting Body Extracts of Trametes Species
指導教授: 郭賓崇
Kuo, Ping-Chung
學位類別: 碩士
Master
系所名稱: 醫學院 - 臨床藥學與藥物科技研究所
Institute of Clinical Pharmacy and Pharmaceutical sciences
論文出版年: 2024
畢業學年度: 112
語文別: 英文
論文頁數: 111
中文關鍵詞: 栓菌屬 、立方栓菌 、香栓菌 、抗發炎活性 、光譜分析
外文關鍵詞: Trametes, Trametes cubensis , Trametes suaveolens , anti-inflammatory activity, spectroscopic analysis
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  • Trametes (栓菌屬) belongs to medically acclaimed family Polyporaceae and includes nearly 195 species. Members of this genus are widely distributed in various biotas throughout the world and have a tradition of use in Chinese medicine for thousands of years. It is considered useful in many aspects of healing, improvement of organ function, energy increase, and so forth. Among the confirmed biological activities, antioxidant, antimicrobial, and anti-inflammatory are the most often mentioned.

    Trametes cubensis (立方栓菌) and Trametes suaveolens (香栓菌) are commonly used edible fungi in Vietnam and belong to the Trametes genus. They mainly grow on living or dead trees. The fruiting bodies of these fungi display various shapes, white color, and are types of saprophytic fungi. T. cubensis exhibited strong anti-HIV-1 activity. In addition, T. suaveolens demonstrated antioxidant, anti-complementary, and anti-HIV-1 bioactivities. However, the relationship between constituents of T. cubensis and T. suaveolens with anti-inflammatory bioactivity was still not clearly established. In the preliminary examination, the methanol extracts of fruiting bodies of T. cubensis and T. suaveolens were subjected to evaluation for their anti-inflammatory bioactivities. The results that T. cubensis promoted superoxide anion generation and elastase release in fMLF/CB-induced human neutrophils, indicated the immunostimulatory effect. Therefore, the present study is aimed to purify and identify the bioactive principles of T. cubensis and T. suaveolens. Totally twenty compounds were isolated from the fruiting body of T. cubensis and T. suaveolens, and their structures were identified through the comparison of their physical and spectroscopic data with those published in the literature. Among these isolates, some compounds were potential according to the literature reports. The purified constituents will be subjected to evaluate their anti-inflammatory bioactivity by human neutrophil model.

    ABSTRACT i ACKNOWLEDGEMENTS ii Table of Contents iii List of Tables iv List of Figures v Chapter 1 Introduction 1 1.1 Research background 1 1.2 Aim of study 4 Chapter 2 Review on pharmacology and constituents of Trametes species 5 2.1 Pharmacology review of Trametes species 5 2.2 Review on constituents of Trametes species 10 Chapter 3 Results and discussion 31 3.1 Purification 31 3.2 Elucidation of important compounds 35 3.3 Identification and spectral data 53 3.4 Discussion of bioactivity of potential constituents 75 Chapter 4 Materials and Methods 78 4.1 General 78 4.2 Fungus materials and authentication 78 4.3 Extraction and isolation 78 Chapter 5 Conclusion and perspective 84 References 85

    1. Yadav, D.; Negi, P. S., Bioactive components of mushrooms: processing effects and health benefits. Food Res. Int. 2021, 148, 110599.
    2. An, G. H.; Han, J. G.; Cho, J. H., Antioxidant activities and β-glucan contents of wild mushrooms in Korea. J. Mushrooms 2019, 17(3), 144-151.
    3. Im, K. H.; Choi, J.; Baek, S. A.; Lee, T. S., Antioxidant and inflammation inhibitory effects from fruiting body extracts of Ganoderma applanatum. J. Mushrooms 2021, 19(4), 261-271.
    4. Chaturvedi, V. K.; Agarwal, S.; Gupta, K. K.; Ramteke, P. W.; Singh, M. P., Medicinal mushroom: boon for therapeutic applications. 3 Biotech 2018, 8(8), 334.
    5. Lee, Y. H.; Kim, M.; Park, H. J.; Park, J. Y.; Song, E. S.; Lee, H.; Ko, G.; Ahn, S.; Kwon, H. W.; Byun, Y.; Kim, C.; Choi, J.; Park, J. T., Chemical screening identifies the anticancer properties of Polyporous parvovarius. J. Cancer 2023, 14(1), 50-60.
    6. Hibbett, D. S.; Binder, M.; Bischoff, J. F.; Blackwell, M.; Cannon, P. F.; Eriksson, O. E.; Huhndorf, S.; James, T.; Kirk, P. M.; Lücking, R.; Lumbsch, H. T.; Lutzoni, F.; Matheny, P. B.; McLaughlin, D. J.; Powell, M. J.; Redhead, S.; Schoch, C. L.; Spatafora, J. W.; Stalpers, J. A.; Vilgalys, R.; Aime, M. C.; Aptroot, A.; Bauer, R.; Begerow, D.; Benny, G. L.; Castlebury, L. A.; Crous, P. W.; Dai, Y. C.; Gams, W.; Geiser, D. M.; Griffith, G. W.; Gueidan, C.; Hawksworth, D. L.; Hestmark, G.; Hosaka, K.; Humber, R. A.; Hyde, K. D.; Ironside, J. E.; Kõljalg, U.; Kurtzman, C. P.; Larsson, K. H.; Lichtwardt, R.; Longcore, J.; Miadlikowska, J.; Miller, A.; Moncalvo, J. M.; Mozley-Standridge, S.; Oberwinkler, F.; Parmasto, E.; Reeb, V.; Rogers, J. D.; Roux, C.; Ryvarden, L.; Sampaio, J. P.; Schüssler, A.; Sugiyama, J.; Thorn, R. G.; Tibell, L.; Untereiner, W. A.; Walker, C.; Wang, Z.; Weir, A.; Weiss, M.; White, M. M.; Winka, K.; Yao, Y. J.; Zhang, N., A higher-level phylogenetic classification of the fungi. Mycol. Res. 2007, 111(5), 509-547.
    7. Ryvarden, L., Genera of polypores, nomenclature and taxonomy. Synopsis Fungorum 1991, 5, 1-363.
    8. Kim, M.; Ahn, C.; Kim, C., Antioxidant activity of indigenous Trametes species in Korea. Kor. J. Mycol. 2021, 49(4), 433-440.
    9. Awadasseid, A.; Hou, J.; Gamallat, Y.; Xueqi, S.; Eugene, K. D.; Musa Hago, A.; Bamba, D.; Meyiah, A.; Gift, C.; Xin, Y., Purification, characterization, and antitumor activity of a novel glucan from the fruiting bodies of Coriolus versicolor. PLoS ONE 2017, 12(2), e0171270.
    10. Hapuarachchi, K. K.; Karunarathna, S. C.; Xu, X. H.; Dutta, A. K.; Phengsintham, P.; Hyde, K. D.; Wen, T. C., A review on bioactive compounds, beneficial properties and biotechnological approaches of Trametes (Polyporaceae, Polyporales) and a new record from Laos. Chiang Mai J. Sci. 2021, 48(3), 674-698.
    11. Muñoz-Castiblanco, T.; Mejía-Giraldo, J. C.; Puertas-Mejía, M. A., Trametes genus, a source of chemical compounds with anticancer activity in human osteosarcoma: a systematic review. J. Appl. Pharm. Sci. 2020, 10(10), 121-129.
    12. Puri, S. C.; Nazir, A.; Chawla, R.; Arora, R.; Riyaz-ul-Hasan, S.; Amna, T.; Ahmed, B.; Verma, V.; Singh, S.; Sagar, R.; Sharma, A.; Kumar, R.; Sharma, R. K.; Qazi, G. N., The endophytic fungus Trametes hirsuta as a novel alternative source of podophyllotoxin and related aryl tetralin lignans. J. Biotechnol. 2006, 122(4), 494-510.
    13. Rashid, S.; Unyayar, A.; Mazmanci, M. A.; McKeown, S. R.; Worthington, J.; Banat, I. M., Potential of a Funalia trogii laccase enzyme as an anticancer agent. Ann. Microbiol. 2015, 65, 175-183.
    14. Nguyen, H. T. K.; Lee, J.; Park, Y.; Park, H. J.; Ahn, S. K.; Kim, J. K.; Kang, D. K.; Kim, M.; Ahn, C.; Kim, C.; Choi, J., Comparative analysis of anticancer and antibacterial activities among seven Trametes species. Mycobiology 2023, 51(4), 256-263.
    15. Coussens, L. M.; Werb, Z., Inflammation and cancer. Nature 2002, 420(6917), 860-867.
    16. Crusz, S. M.; Balkwill, F. R., Inflammation and cancer: advances and new agents. Nat. Rev. Clin. Oncol. 2015, 12(10), 584-596.
    17. Singh, N.; Baby, D.; Rajguru, J. P.; Patil, P. B.; Thakkannavar, S. S.; Pujari, V. B., Inflammation and cancer. Ann. Afr. Med. 2019, 18(3), 121-126.
    18. Greten, F. R.; Grivennikov, S. I., Inflammation and cancer: triggers, mechanisms, and consequences. Immunity 2019, 51(1), 27-41.
    19. Barton, G. M., A calculated response: control of inflammation by the innate immune system. J. Clin. Invest. 2008, 118(2), 413-420.
    20. Libby, P., Inflammatory mechanisms: the molecular basis of inflammation and disease. Nutr. Rev. 2007, 65(12), S140-S146.
    21. Pan, M. H.; Lai, C. S.; Ho, C. T., Anti-inflammatory activity of natural dietary flavonoids. Food Funct. 2010, 1(1), 15-31.
    22. Hwang, T. L.; Li, G. L.; Lan, Y. H.; Chia, Y. C.; Hsieh, P. W.; Wu, Y. H.; Wu, Y. C., Potent inhibition of superoxide anion production in activated human neutrophils by isopedicin, a bioactive component of the Chinese medicinal herb Fissistigma oldhamii. Free Radic. Biol. Med. 2009, 46(4), 520-528.
    23. Ennis, M., Neutrophils in asthma pathophysiology. Curr. Allergy Asthma Rep. 2003, 3(2), 159-165.
    24. Malech, H. L.; Gallin, J. I., Current concepts: immunology. Neutrophils in human diseases. N. Engl. J. Med. 1987, 317(11), 687-694.
    25. Okajima, K.; Harada, N.; Uchiba, M., Ranitidine reduces ischemia/reperfusion-induced liver injury in rats by inhibiting neutrophil activation. J. Pharmacol. Exp. Ther. 2002, 301(3), 1157-1165.
    26. Vinten-Johansen, J., Involvement of neutrophils in the pathogenesis of lethal myocardial reperfusion injury. Cardiovasc. Res. 2004, 61(3), 481-497.
    27. Witko-Sarsat, V.; Rieu, P.; Descamps-Latscha, B.; Lesavre, P.; Halbwachs-Mecarelli, L., Neutrophils: molecules, functions and pathophysiological aspects. Lab. Invest. 2000, 80(5), 617-653.
    28. Kakoti, M.; Dullah, S.; Hazarika, D. J.; Barooah, M.; Boro, R. C., Cinnabarinic acid from Trametes coccinea fruiting bodies exhibits antibacterial activity through inhibiting the biofilm formation. Arch. Microbiol. 2022, 204(3), 173.
    29. Dávila Giraldo, L. R.; Pérez Jaramillo, C. C.; Méndez Arteaga, J. J.; Murillo-Arango, W., Nutritional value and antioxidant, antimicrobial and cytotoxic activity of wild macrofungi. Microorganisms 2023, 11(5), 1158.
    30. Li, Y. C.; Ngan, N. T.; Cheng, K. C.; Hwang, T. L.; Thang, T. D.; Tuan, N. N.; Yang, M. L.; Kuo, P. C.; Wu, T. S., Constituents from the fruiting bodies of Trametes cubensis and Trametes suaveolens in Vietnam and their anti-inflammatory bioactivity. Molecules 2021, 26(23), 7311.
    31. Appiah, T.; Agyare, C.; Luo, Y.; Boamah, V. E.; Boakye, Y. D., Antimicrobial and resistance modifying activities of cerevisterol isolated from Trametes species. Curr. Bioact. Compd. 2020, 16(2), 115-123.
    32. Gebreyohannes, G.; Sbhatu, D. B.; Nyerere, A.; Bii, C.; Gebrehiwot, A. G., Wild mushrooms: potential natural sources of antioxidant and anti-quorum sensing bioactive compounds for medical applications. Evid. Based Complement. Alternat. Med. 2023, 2023, 6141646.
    33. Knežević, A.; Stajić, M.; Sofrenić, I.; Stanojković, T.; Milovanović, I.; Tešević, V.; Vukojević, J., Antioxidative, antifungal, cytotoxic and antineurodegenerative activity of selected Trametes species from Serbia. PLoS ONE 2018, 13(8), e0203064.
    34. Ma, Y.; Mao, D.; Geng, L.; Wang, Z.; Xu, C., Production, fractionation, characterization of extracellular polysaccharide from a newly isolated Trametes gibbosa and its hypoglycemic activity. Carbohydr. Polym. 2013, 96(2), 460-465.
    35. Jouybari, H. B.; Valadan, R.; Mirzaee, F.; Karizno, F. B.; Habibi, E., Immunomodulatory activity of polysaccharide from Trametes gibbosa (Pers.) Fr (Basidiomycota, Fungi) mediated by TLR4 signaling pathway. Adv. Biomed. Res. 2023, 12, 127.
    36. He, N.; Tian, L.; Zhai, X.; Zhang, X.; Zhao, Y., Composition characterization, antioxidant capacities and anti-proliferative effects of the polysaccharides isolated from Trametes lactinea (Berk.) Pat. Int. J. Biol. Macromol. 2018, 115, 114-123.
    37. Zhang, Q.; Wang, J.; He, H.; Liu, H.; Yan, X.; Zou, K., Trametenolic acid B reverses multidrug resistance in breast cancer cells through regulating the expression level of P‐glycoprotein. Phytother. Res. 2014, 28(7), 1037-1044.
    38. Zhang, Q.; Huang, N.; Wang, J.; Luo, H.; He, H.; Ding, M.; Deng, W. Q.; Zou, K., The H+/K+-ATPase inhibitory activities of Trametenolic acid B from Trametes lactinea (Berk.) Pat, and its effects on gastric cancer cells. Fitoterapia 2013, 89, 210-217.
    39. León, F.; Brouard, I.; Rivera, A.; Torres, F.; Rubio, S.; Quintana, J.; Estévez, F.; Bermejo, J., Isolation, structure elucidation, total synthesis, and evaluation of new natural and synthetic ceramides on human SK-MEL-1 melanoma cells. J. Med. Chem. 2006, 49(19), 5830-5839.
    40. Ohshiro, T.; Namatame, I.; Ochiai, K.; Kawagishi, H.; Tomoda, H., Inhibition of lipid droplet accumulation in macrophages by triterpenoids produced from Trametes orientalis. Biol. Pharm. Bull. 2005, 28(10), 1925-1927.
    41. Zhou, L.; Lu, B.; Sun, Y., Glucose-lowering effect of Trametes orientalis polysaccharides in hyperglycemic and hyperlipidemic mice. J. South. Med. Univ. (Nan Fang Yi Ke Da Xue Xue Bao, 南方医科大学学报) 2020, 40(8), 1127-1133.
    42. Zheng, Y.; Li, Y; Wang, W. D., Optimization of ultrasonic-assisted extraction and in vitro antioxidant activities of polysaccharides from Trametes orientalis. Carbohydr. Polym. 2014, 111, 315-323.
    43. Zheng, Y.; Fan, J.; Chen, H. W.; Liu, E. Q., Trametes orientalis polysaccharide alleviates PM2.5-induced lung injury in mice through its antioxidant and anti-inflammatory activities. Food Funct. 2019, 10(12), 8005-8015.
    44. Zheng, Y.; Cui, J.; Chen, A. H.; Zong, Z. M.; Wei, X. Y., Optimization of ultrasonic-microwave assisted extraction and hepatoprotective activities of polysaccharides from Trametes orientalis. Molecules 2019, 24(1), 147.
    45. Zheng, Y.; Wang, W. D.; Li, Y., Antitumor and immunomodulatory activity of polysaccharide isolated from Trametes orientalis. Carbohydr. Polym. 2015, 131, 248-254.
    46. Zheng, Y.; Zong, Z. M.; Chen, S. L.; Chen, A. H.; Wei, X. Y., Ameliorative effect of Trametes orientalis polysaccharide against immunosuppression and oxidative stress in cyclophosphamide-treated mice. Int. J. Biol. Macromol. 2017, 95, 1216-1222.
    47. Kurniawan, B.; Bankeeree, W.; Yanatatsaneejit, P.; Prasongsuk, S., Antiproliferative activity and apoptosis‑inducing effects of Trametes polyzona polysaccharides against human breast cancer cells. Biomed. Rep. 2023, 19(5), 83.
    48. Im, K. H.; Nguyen, T. K.; Choi, J.; Lee, T. S., In vitro antioxidant, anti-diabetes, anti-dementia, and inflammation inhibitory effect of Trametes pubescens fruiting body extracts. Molecules 2016, 21(5), 639.
    49. Gou, Y.; Zheng, X.; Li, W.; Deng, H.; Qin, S., Polysaccharides produced by the mushroom Trametes robiniophila Murr boosts the sensitivity of hepatoma cells to oxaliplatin via the miR-224-5p/ABCB1/P-gp axis. Integr. Cancer Ther. 2022, 21, 15347354221090221.
    50. Pan, J.; Yang, C.; Jiang, Z.; Huang, J., Trametes robiniophila Murr: a traditional Chinese medicine with potent anti-tumor effects. Cancer Manag. Res. 2019, 11, 1541-1549.
    51. Song, X.; Li, Y.; Zhang, H.; Yang, Q., The anticancer effect of Huaier (Review). Oncol. Rep. 2015, 34(1), 12-21.
    52. Xu, D. Q.; Yuan, X. J.; Toyoda, H.; Hirayama, M., Anti-tumor effect of Huaier extract against neuroblastoma cells in vitro. Int. J. Med. Sci. 2021, 18(4), 1015-1023.
    53. Pan, J.; Jiang, Z.; Wu, D.; Yang, C.; Wang, Z.; Huang, J., Huaier extractum promotes dendritic cells maturation and favors them to induce ThI immune response: one of the mechanisms underlying its anti-tumor activity. Integr. Cancer Ther. 2020, 19, 1534735420946830.
    54. Chen, J.; Chen, S.; Zhou, Y.; Wang, S.; Wu, W., Efficacy and safety of huaier granule as an adjuvant therapy for cancer: an overview of systematic reviews and meta-analyses. Integr. Cancer Ther. 2022, 21, 15347354221083910.
    55. Sun, Y.; Sun, T.; Wang, F.; Zhang, J.; Li, C.; Chen, X.; Li, Q.; Sun, S., A polysaccharide from the fungi of Huaier exhibits anti-tumor potential and immunomodulatory effects. Carbohydr. Polym. 2013, 92(1), 577-582.
    56. Wang, X.; Zhang, N.; Huo, Q.; Yang, Q., Anti-angiogenic and antitumor activities of Huaier aqueous extract. Oncol. Rep. 2012, 28(4), 1167-1175.
    57. Liu, X.; Liu, L.; Chen, K.; Sun, L.; Li, W.; Zhang, S., Huaier shows anti‐cancer activities by inhibition of cell growth, migration and energy metabolism in lung cancer through PI3K/AKT/HIF‐1α pathway. J. Cell. Mol. Med. 2021, 25(4), 2228-2237.
    58. Su, D.; Jiang, B.; Yang, Y.; Miao, Y.; Fu, Q.; Zhang, F., Effect of Huaier on melanoma invasion, metastasis, and angiogenesis. BioMed Res. Int. 2020, 2020, 8163839.
    59. Xu, D. Q.; Yuan, X. J.; Hirayama, M.; Toyoda, H., Huaier extract induces apoptosis in hepatoblastoma cells via the MEK/ERK signaling pathway. In Vivo 2020, 34(5), 2381-2388.
    60. Ding, X.; Yang, Q.; Kong, X.; Haffty, B. G.; Gao, S.; Moran, M. S., Radiosensitization effect of Huaier on breast cancer cells. Oncol. Rep. 2016, 35(5), 2843-2850.
    61. Li, C.; Wang, X.; Chen, T.; Wang, W.; Yang, Q., Trametes robiniophila Murr in the treatment of breast cancer. Biomed. Pharmacother. 2020, 128, 110254.
    62. Yao, X.; Wu, W.; Qu, K.; Xi, W., Traditional Chinese biomedical preparation (Huaier Granule) for breast cancer: a PRISMA-compliant meta-analysis. Biosci. Rep. 2020, 40(8), BSR20202509.
    63. Zhang, N.; Kong, X.; Yan, S.; Yuan, C.; Yang, Q., Huaier aqueous extract inhibits proliferation of breast cancer cells by inducing apoptosis. Cancer Sci. 2010, 101(11), 2375-2383.
    64. Wang, J.; Wang, X.; Chen, T.; Jiang, L.; Yang, Q., Huaier extract inhibits breast cancer progression through a LncRNA-H19/MiR-675-5p pathway. Cell. Physiol. Biochem. 2017, 44(2), 581-593.
    65. Li, Y.; Qi, W.; Song, X.; Lv, S.; Zhang, H.; Yang, Q., Huaier extract suppresses breast cancer via regulating tumor-associated macrophages. Sci. Rep. 2016, 6, 20049.
    66. Wang, X.; Zhang, N.; Huo, Q.; Sun, M.; Lv, S.; Yang, Q., Huaier aqueous extract suppresses human breast cancer cell proliferation through inhibition of estrogen receptor α signaling. Int. J. Oncol. 2013, 43(1), 321-328.
    67. Wang, X.; Qi, W.; Li, Y.; Zhang, N.; Dong, L.; Sun, M.; Cun, J.; Zhang, Y.; Lv, S.; Yang, Q., Huaier extract induces autophagic cell death by inhibiting the mTOR/S6K pathway in breast cancer cells. PLoS ONE 2015, 10(7), e0131771.
    68. Zhang, Y.; Wang, X.; Chen, T., Efficacy of Huaier granule in patients with breast cancer. Clin. Transl. Oncol. 2019, 21(5), 588-595.
    69. Hu, B.; Yan, W.; Wang, M.; Cui, X.; Hu, Y.; Chen, Q.; Zhang, Y.; Qi, X.; Jiang, J., Huaier polysaccharide inhibits the stem-like characteristics of ERα-36high triple negative breast cancer cells via inactivation of the ERα-36 signaling pathway. Int. J. Biol. Sci. 2019, 15(7), 1358-1367.
    70. Wang, X.; Zhang, N.; Huo, Q.; Sun, M.; Dong, L.; Zhang, Y.; Xu, G.; Yang, Q., Huaier aqueous extract inhibits stem-like characteristics of MCF7 breast cancer cells via inactivation of hedgehog pathway. Tumor Biol. 2014, 35(11), 10805-10813.
    71. Luo, Z.; Hu, X.; Xiong, H.; Qiu, H.; Yuan, X.; Zhu, F.; Wang, Y.; Zou, Y., A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein. Carbohydr. Polym. 2016, 151, 1027-1033.
    72. Qi, W.; Sun, M.; Kong, X.; Li, Y.; Wang, X.; Lv, S.; Ding, X.; Gao, S.; Cun, J.; Cai, C.; Wang, X.; Chen, J.; Yin, A.; Yang, Q., Huaier extract synergizes with tamoxifen to induce autophagy and apoptosis in ER-positive breast cancer cells. Oncotarget 2016, 7(18), 26003-26015.
    73. Gao, S.; Li, X.; Ding, X.; Jiang, L.; Yang, Q., Huaier extract restrains the proliferative potential of endocrine-resistant breast cancer cells through increased ATM by suppressing miR-203. Sci. Rep. 2017, 7(1), 7313.
    74. Li, C.; Wang, X.; Chen, T.; Li, W.; Zhou, X.; Wang, L.; Yang, Q., Huaier induces immunogenic cell death via CircCLASP1/PKR/eIF2α signaling pathway in triple negative breast cancer. Front. Cell Dev. Biol. 2022, 10, 913824.
    75. Wu, T.; Chen, W.; Liu, S.; Lu, H.; Wang, H.; Kong, D.; Huang, X.; Kong, Q.; Ning, Y.; Lu, Z., Huaier suppresses proliferation and induces apoptosis in human pulmonary cancer cells via upregulation of miR-26b-5p. FEBS Lett. 2014, 588(12), 2107-2114.
    76. Gan, H. Z.; Xu, X. X.; Bai, Y. Y., Trametes robiniophila represses angiogenesis and tumor growth of lung cancer via strengthening let-7d-5p and targeting NAP1L1. Bioengineered 2022, 13(3), 6698-6710.
    77. Chen, Y.; Wu, H.; Wang, X.; Wang, C; Gan, L.; Zhu, J.; Tong, J.; Li, Z., Huaier Granule extract inhibit the proliferation and metastasis of lung cancer cells through down-regulation of MTDH, JAK2/STAT3 and MAPK signaling pathways. Biomed. Pharmacother. 2018, 101, 311-321.
    78. Lv, F.; Li, X.; Wang, Y., An extraction from Trametes robiniophila Murr. (Huaier) inhibits non-small cell lung cancer proliferation via targeting to epidermal growth factor receptor. Bioengineered 2022, 13(4), 10931-10943.
    79. Tian, Y. Y.; Yang, A. L.; Chen, X. N.; Ren, H. M.; Liu, Y. X.; Qiu, H. L.; Tang, L. M. Y.; Huang, H. M.; Tu, P. F.; Hu, Z. D., Effect of Huaier aqueous extract on growth and metastasis of human non-small cell lung cancer NCI-H1299 cells and its underlying mechanisms. China J. Chin. Mater. Med. (Zhongguo Zhong Yao Za Zhi, 中国中药杂志) 2020, 45(15), 3700-3706.
    80. Xie, J.; Zhuan, B.; Wang, H.; Wang, Y.; Wang, X.; Yuan, Q.; Yang, Z., Huaier extract suppresses non‐small cell lung cancer progression through activating NLRP3‐dependent pyroptosis. Anat. Rec. 2021, 304(2), 291-301.
    81. Zhang, R. R.; Shao, M. Y.; Fu, Y.; Zhao, R. X.; Wang, J. W.; Li, M.; Zhao, Y. X.; Shao, F. L., Systematic evaluation of Huaier granules adjuvant treatment of primary liver cancer. China J. Chin. Mater. Med. (Zhongguo Zhong Yao Za Zhi, 中国中药杂志) 2021, 46(2), 478-487.
    82. Ma, Y.; Wang, C.; Zhang, Q.; Peng, X.; Feng, Y.; Meng, X., The effects of polysaccharides from Auricularia auricula (Huaier) in adjuvant anti-gastrointestinal cancer therapy: a systematic review and network meta-analysis. Pharmacol. Res. 2018, 132, 80-89.
    83. Li, B.; Cao, Q.; Liu, Z., The treatment effects of Trametes robiniophila Murr against colorectal cancer: a mini-review. Front. Med. 2022, 9, 981516.
    84. Yang, A.; Zhao, Y.; Wang, Y.; Zha, X.; Zhao, Y.; Tu, P.; Hu, Z. Huaier suppresses proliferative and metastatic potential of prostate cancer PC3 cells via downregulation of Lamin B1 and induction of autophagy. Oncol. Rep. 2018, 39(6), 3055-3063.
    85. Zhou, C.; Li, J.; Qian, W.; Yue, Y.; Xiao, Y.; Qin, T.; Ma, Q.; Li, X., Huaier extract restrains pancreatic cancer by suppressing Wnt/β-catenin pathway. Biomed. Pharmacother. 2020, 127, 110126.
    86. Fu, Z.; Ma, K.; Dong, B.; Zhao, C.; Che, C.; Dong, C.; Zhang, R.; Wang, H.; Wang, X.; Liang, R., The synergistic antitumor effect of Huaier combined with 5-fluorouracil in human cholangiocarcinoma cells. BMC Complement. Altern. Med. 2019, 19(1), 203.
    87. Hu, Z.; Yang, A.; Su, G.; Zhao, Y.; Wang, Y.; Chai, X.; Tu, P., Huaier restrains proliferative and invasive potential of human hepatoma SKHEP-1 cells partially through decreased Lamin B1 and elevated NOV. Sci. Rep. 2016, 6, 31298.
    88. Yang, A. L.; Xia, T. J.; Zhao, Y. N.; Song, J. Y.; Shen, H. R.; Xu, Z. H.; Tu, P. F.; Hu, Z. D., Huaier aqueous extract inhibits proliferation of human hepatoma SK-HEP-1 cells through up-regulation of autophagy. China J. Chin. Mater. Med. (Zhongguo Zhong Yao Za Zhi, 中国中药杂志) 2018, 43(3), 591-595.
    89. Zhang, F.; Zhang, Z.; Liu, Z., Effects of Huaier aqueous extract on proliferation and apoptosis in the melanoma cell line A875. Acta Histochem. 2013, 115(7), 705-711.
    90. Yang, A.; Fan, H.; Zhao, Y.; Zha, X.; Zhang, H.; Hu, Z.; Tu, P., Huaier aqueous extract inhibits proliferation and metastasis of tuberous sclerosis complex cell models through downregulation of JAK2/STAT3 and MAPK signaling pathways. Oncol. Rep. 2016, 36(3), 1491-1498.
    91. Guo, Y.; Wang, M.; Mou, J.; Zhao, Z.; Yang, J.; Zhu, F.; Pei, G.; Zhu, H.; Wang, Y.; Xu, G.; Zeng, R.; Yao, Y., Pretreatment of Huaiqihuang extractum protects against cisplatin-induced nephrotoxicity. Sci. Rep. 2018, 8(1), 7333.
    92. Fang, L.; Zhang, Y.; Wang, Q.; Zang, Y.; Li, Z.; Duan, Z.; Ren, J.; Xu, Z., A polysaccharide from Huaier ameliorates cisplatin nephrotoxicity by decreasing oxidative stress and apoptosis via PI3K/AKT signaling. Int. J. Biol. Macromol. 2019, 139, 932-943.
    93. Sun, W. W.; Dou, J. X.; Zhang, L.; Qiao, L. K.; Shen, N.; Gao, W. Y., Killing effect of Huaier combined with DC-CIK on nude mice bearing colon cancer HT29 stem cells in vivo. China J. Chin. Mater. Med. (Zhongguo Zhong Yao Za Zhi, 中国中药杂志) 2018, 43(1), 168-173.
    94. Wang, Y.; Lv, H.; Xu, Z.; Sun, J.; Ni, Y.; Chen, Z.; Cheng, X., Huaier n-butanol extract suppresses proliferation and metastasis of gastric cancer via c-Myc-Bmi1 axis. Sci. Rep. 2019, 9(1), 447.
    95. Shi, Y.; Yuan, L.; Xu, J.; Xu, H.; Wang, L.; Huang, L.; Xu, Z.; Cheng, X., Huaier inhibits gastric cancer growth and hepatic metastasis by reducing syntenin expression and STAT3 phosphorylation. J. Oncol. 2022, 2022, 6065516.
    96. Yan, X.; Lyu, T.; Jia, N.; Yu, Y.; Hua, K.; Feng, W., Huaier aqueous extract inhibits ovarian cancer cell motility via the AKT/GSK3β/β-catenin pathway. PLoS ONE 2013, 8(5), e63731.
    97. Zhao, X.; Ma, S.; Liu, N.; Liu, J.; Wang, W., A polysaccharide from Trametes robiniophila inhibits human osteosarcoma xenograft tumor growth in vivo. Carbohydr. Polym. 2015, 124, 157-163.
    98. Zhao, X.; Ma, S.; Liu, N.; Liu, J.; Wang, W., A polysaccharide from Trametes robiniophila Murrill induces apoptosis through intrinsic mitochondrial pathway in human osteosarcoma (U-2 OS) cells. Tumor Biol. 2015, 36(7), 5255-5263.
    99. Wang, L.; Xu, L.; Wang, Y., Huaier inhibits proliferation, migration, and invasion of cutaneous squamous cell carcinoma cells by inhibiting the methylation levels of CDKN2A and TP53. Integr. Cancer Ther. 2021, 20, 1-9.
    100. Su, D.; Zhang, X.; Zhang, L.; Zhou, J.; Zhang, F., A randomized, double-blind, controlled clinical study on the curative effect of Huaier on mild-to-moderate psoriasis and an experimental study on the proliferation of Hacat cells. BioMed Res. Int. 2018, 2018, 2372895.
    101. Ren, J.; Zheng, C.; Feng, G.; Liang, H.; Xia, X.; Fang, J.; Duan, X.; Zhao, H., Inhibitory effect of extract of fungi of Huaier on hepatocellular carcinoma cells. J. Huazhong Univ. Sci. Technol. Med. Sci. 2009, 29(2), 198-201.
    102. Chen, Q.; Shu, C.; Laurence, A. D.; Chen, Y.; Peng, B. G.; Zhen, Z. J.; Cai, J. Q.; Ding, Y. T.; Li, L. Q.; Zhang, Y. B.; Zheng, Q. C.; Xu, G. L.; Li, B.; Zhou, W. P.; Cai, S. W.; Wang, X. Y.; Wen, H.; Peng, X. Y.; Zhang, X. W.; Dai, C. L.; Bie, P.; Xing, B. C.; Fu, Z. R.; Liu, L. X.; Mu, Y.; Zhang, L.; Zhang, Q. S.; Jiang, B.; Qian, H. X.; Wang, Y. J.; Liu, J. F.; Qin, X. H.; Li, Q.; Yin, P.; Zhang, Z. W.; Chen, X. P., Effect of Huaier granule on recurrence after curative resection of HCC: a multicentre, randomised clinical trial. Gut 2018, 67(11), 2006-2016.
    103. Yang, A.; Fan, H.; Zhao, Y.; Chen, X.; Zhu, Z.; Zha, X.; Zhao, Y.; Chai, X.; Li, J.; Tu, P.; Hu, Z. An immune-stimulating proteoglycan from the medicinal mushroom Huaier up-regulates NF-κB and MAPK signaling via Toll-like receptor 4. J. Biol. Chem. 2019, 294(8), 2628-2641.
    104. Long, H.; Wu, Z., Immunoregulatory effects of Huaier (Trametes robiniophila Murr) and relevant clinical applications. Front. Immunol. 2023, 14, 1147098.
    105. Zhao, G. S.; Liu, Y.; Zhang, Q.; Li, C.; Zhang, Y. W.; Ren, Z. Z.; Zhou, J.; Zhang, M., Transarterial chemoembolization combined with Huaier granule for the treatment of primary hepatic carcinoma: safety and efficacy. Medicine 2017, 96(29), e7589.
    106. Qu, P.; Zhou, F.; Tan, L. F.; Wang, Z. J.; Wang, M. L.; Jin, R. M.; Han, J., Effect of Huaier aqueous extract combined with routine chemo-therapeutic drugs on human acute lymphoblastic leukemia cells Nalm-6 and Sup-B15. J. Exp. Hematol. (Zhongguo Shi Yan Xue Ye Xue Za Zhi, 中国实验血液学杂志) 2020, 28(5), 1451-1458.
    107. Qu, P.; Han, J.; Qiu, Y.; Yu, H.; Hao, J.; Jin, R.; Zhou, F., Huaier extract enhances the treatment efficacy of imatinib in Ik6+ Ph+ acute lymphoblastic leukemia. Biomed. Pharmacother. 2019, 117, 109071.
    108. Yuan, B.; Yin, C.; Ye, X.; Bai, Z.; Lu, Z.; Li, X.; Al-Azab, M.; Mu, L.; Li, W., Differential effects of Huaier aqueous extract on human CD4+T lymphocytes from patients with primary immune thrombocytopenia. Exp. Hematol. 2021, 101, 58-67.
    109. Zhang, Z.; Shen, C.; Zhou, F., The natural medicinal fungus Huaier promotes the anti-hepatoma efficacy of sorafenib through the mammalian target of rapamycin-mediated autophagic cell death. Med. Oncol. 2022, 39(12), 221.
    110. Wang, Z.; Yu, X. L.; Zhang, J.; Cheng, Z. G.; Han, Z. Y.; Liu, F. Y.; Dou, J. P.; Kong, Y.; Dong, X. J.; Zhao, Q. X.; Yu, J.; Liang, P.; Tang, W. Z., Huaier granule prevents the recurrence of early-stage hepatocellular carcinoma after thermal ablation: a cohort study. J. Ethnopharmacol. 2021, 281, 114539.
    111. Huan, C.; Yao, J.; Xu, W.; Zhang, W.; Zhou, Z.; Pan, H.; Gao, S., Huaier polysaccharide interrupts PRV infection via reducing virus adsorption and entry. Viruses 2022, 14(4), 745.
    112. Zhao, J. Y.; Wu, Y. B., Huaier extract attenuates acute kidney injury to chronic kidney disease transition by inhibiting endoplasmic reticulum stress and apoptosis via miR-1271 upregulation. BioMed Res. Int. 2020, 2020, 9029868.
    113. Lv, H.; Jiang, Y.; Liao, M.; Sun, H.; Zhang, S.; Peng, X., In vitro and in vivo treatments of Echinococcus granulosus with Huaier aqueous extract and albendazole liposome. Parasitol. Res. 2013, 112(1), 193-198.
    114. Ma, X.; Gao, H.; Yang, B.; Zhao, H.; Zhu, Z., Huaier polysaccharide attenuates doxorubicin-induced acute cardiotoxicity by regulating ferroptosis. Bull. Exp. Biol. Med. 2022, 174(1), 37-42.
    115. Li, L. T.; Shi, M. Y.; Wei, S. Y.; Li, T.; Li, B., Huai Qi Huang ameliorates proteinuria and hematuria in mild IgA nephropathy patients: a prospective randomized controlled study. J. Formos. Med. Assoc. 2013, 112(12), 766-772.
    116. Xu, J. L.; Yuan, L.; Hu, C.; Weng, C. Y.; Xu, H. D.; Shi, Y. F; Huang, L.; Ying, J. E.; Xu, Z. Y.; Qin, J. J.; Cheng, X. D, Trametes robiniophila Murr sensitizes gastric cancer cells to 5-fluorouracil by modulating tumor microenvironment. Front. Pharmacol. 2022, 13, 911663.
    117. Geng, W.; Tu, C.; Chen, D.; Lu, Z.; Mao, W.; Zhu, H., Huaier attenuates the adverse effects of pyroptosis by regulating the methylation of rat mesangial cells: an in vitro study. BMC Complement. Med. Ther. 2022, 22, 92.
    118. Zhang, M.; Yan, M.; Yang, J.; Li, F.; Wang, Y.; Feng, K.; Wang, S.; Lin, N.; Wang, Y.; Yang, B., Structural characterization of a polysaccharide from Trametes sanguinea Lloyd with immune-enhancing activity via activation of TLR4. Int. J. Biol. Macromol. 2022, 206, 1026-1038.
    119. Yan, M.; Zhang, M.; Zhu, Z.; Zhang, J.; Cheng, G.; Lin, N.; Zhao, H.; Yang, B., Structural characterization and tumor microvascular inhibition activity of total polysaccharide from Trametes sanguinea Lloyd. Chem. Biodivers. 2022, 19(3), e202100765.
    120. Rashid, S.; Unyayar, A.; Mazmanci, M. A.; McKeown, S. R.; Banat, I. M.; Worthington, J., A study of anti-cancer effects of Funalia trogii in vitro and in vivo. Food Chem. Toxicol. 2011, 49(7), 1477-1483.
    121. Wang, S. R.; Zhang, L.; Chen, H. P.; Li, Z. H.; Dong, Z. J.; Wei, K.; Liu, J. K., Four new spiroaxane sesquiterpenes and one new rosenonolactone derivative from cultures of Basidiomycete Trametes versicolor. Fitoterapia 2015, 105, 127-131.
    122. Wu, J. M.; Doonan, B. B.; Hsieh, T. C.; Yang, Q.; Yang, X. T.; Ling, M. T. Recent advances and challenges in studies of control of cancer stem cells and the gut microbiome by the Trametes-derived polysaccharopeptide PSP (Review). Int. J. Med. Mushrooms 2016, 18(8), 651-660.
    123. Luo, K. W.; Yue, G. G. L.; Ko, C. H.; Lee, J. K. M.; Gao, S.; Li, L. F.; Li, G.; Fung, K. P.; Leung, P. C.; Lau, C. B. S., In vivo and in vitro anti-tumor and anti-metastasis effects of Coriolus versicolor aqueous extract on mouse mammary 4T1 carcinoma. Phytomedicine 2014, 21(8-9), 1078-1087.
    124. Leliebre-Lara, V.; Monzote Fidalgo, L.; Pferschy-Wenzig, E.-M.; Kunert, O.; Nogueiras Lima, C.; Bauer, R., In vitro antileishmanial activity of sterols from Trametes versicolor (Bres. Rivarden). Molecules 2016, 21(8), 1045.
    125. Leliebre-Lara, V.; García, M.; Nogueiras, C.; Monzote, L., Qualitative analysis of an ethanolic extract from Trametes versicolor and biological screening against Leishmania amazonensis. Emir. J. Food Agric. 2015, 27(7), 592-595.
    126. Jhan, M. H.; Yeh, C. H.; Tsai, C. C.; Kao, C. T.; Chang, C. K.; Hsieh, C. W., Enhancing the antioxidant ability of Trametes versicolor polysaccharopeptides by an enzymatic hydrolysis process. Molecules 2016, 21(9), 1215.
    127. Sun, X.; Sun, Y.; Zhang, Q.; Zhang, H.; Yang, B.; Wang, Z.; Zhu, W.; Li, B.; Wang, Q.; Kuang, H., Screening and comparison of antioxidant activities of polysaccharides from Coriolus versicolor. Int. J. Biol. Macromol. 2014, 69, 12-19.
    128. Scarpari, M.; Reverberi, M.; Parroni, A.; Scala, V.; Fanelli, C.; Pietricola, C.; Zjalic, S.; Maresca, V.; Tafuri, A.; Ricciardi, M. R.; Licchetta, R.; Mirabilii, S.; Sveronis, A.; Cescutti, P.; Rizzo, R., Tramesan, a novel polysaccharide from Trametes versicolor. Structural characterization and biological effects. PLoS ONE 2017, 12(8), e0171412.
    129. Smith, H.; Doyle, S.; Murphy, R., Filamentous fungi as a source of natural antioxidants. Food Chem. 2015, 185, 389-397.
    130. Chen, J.; Jin, X.; Zhang, L.; Yang, L., A study on the antioxidant effect of Coriolus versicolor polysaccharide in rat brain tissues. Afr. J. Tradit. Complement. Altern. Med. 2013, 10(6), 481-484.
    131. Rašeta, M.; Popović, M.; Knežević, P.; Šibul, F.; Kaišarević, S.; Karaman, M., Bioactive phenolic compounds of two medicinal mushroom species Trametes versicolor and Stereum subtomentosum as antioxidant and antiproliferative agents. Chem. Biodivers. 2020, 17(12), e2000683.
    132. Kozarski, M.; Klaus, A.; Nikšić, M.; Vrvić, M. M.; Todorović, N.; Jakovljević, D.; Van Griensven, L. J., Antioxidative activities and chemical characterization of polysaccharide extracts from the widely used mushrooms Ganoderma applanatum, Ganoderma lucidum, Lentinus edodes and Trametes versicolor. J. Food Compos. Anal. 2012, 26(1-2), 144-153.
    133. Orhan, I.; Üstün, O., Determination of total phenol content, antioxidant activity and acetylcholinesterase inhibition in selected mushrooms from Turkey. J. Food Compos. Anal. 2011, 24(3), 386-390.
    134. Kamiyama, M.; Horiuchi, M.; Umano, K.; Kondo, K.; Otsuka, Y.; Shibamoto, T., Antioxidant/anti-inflammatory activities and chemical composition of extracts from the mushroom Trametes versicolor. Int. J. Nutr. Food Sci. 2013, 2(2), 85-91.
    135. Karaman, M.; Jovin, E.; Malbaša, R.; Matavuly, M.; Popović, M., Medicinal and edible lignicolous fungi as natural sources of antioxidative and antibacterial agents. Phytother. Res. 2010, 24(10), 1473-1481.
    136. Michalak, K.; Winiarczyk, S.; Adaszek, Ł.; Kosikowska, U.; Andrzejczuk, S.; Garbacz, K.; Dobrut, A.; Jarosz, Ł.; Czupryna, W.; Pietras-Ożga, D., Antioxidant and antimicrobial properties of an extract rich in proteins obtained from Trametes versicolor. J. Vet. Res. 2023, 67(2), 209-218.
    137. Lowenthal, R.; Taylor, M.; Gidden, J. A.; Heflin, B.; Lay Jr, J. O.; Avaritt, N.; Tackett, A. J.; Urbaniak, A., The mycelium of the Trametes versicolor synn. Coriolus versicolor (Turkey tail mushroom) exhibit anti-melanoma activity in vitro. Biomed. Pharmacother. 2023, 161, 114424.
    138. Valisolalao, J.; Luu, B.; Ourisson, G., Steroides cytotoxiques de Polyporus versicolor. Tetrahedron 1983, 39(17), 2779-2785.
    139. Shnyreva, A. V.; Shnyreva, A. A.; Espinoza, C.; Padrón, J. M.; Trigos, Á., Antiproliferative activity and cytotoxicity of some medicinal wood-destroying mushrooms from Russia. Int. J. Med. Mushrooms 2018, 20(1), 1-11.
    140. He, Z.; Lin, J.; He, Y.; Liu, S., Polysaccharide-peptide from Trametes versicolor: the potential medicine for colorectal cancer treatment. Biomedicines 2022, 10(11), 2841.
    141. Janjušević, L.; Karaman, M.; Šibul, F.; Tommonaro, G.; Iodice, C.; Jakovljević, D.; Pejin, B., The lignicolous fungus Trametes versicolor (L.) Lloyd (1920): a promising natural source of antiradical and AChE inhibitory agents. J. Enzyme Inhib. Med. Chem. 2017, 32(1), 355-362.
    142. Donatini, B., Control of oral human papillomavirus (HPV) by medicinal mushrooms, Trametes versicolor and Ganoderma lucidum: a preliminary clinical trial. Int. J. Med. Mushrooms 2014, 16(5), 497-498.
    143. Rokos, T.; Pribulova, T.; Kozubik, E.; Biringer, K.; Holubekova, V.; Kudela, E., Exploring the bioactive mycocompounds (fungal compounds) of selected medicinal mushrooms and their potentials against HPV infection and associated cancer in humans. Life 2023, 13(1), 244.
    144. Arunachalam, K.; Sasidharan, S. P.; Yang, X., A concise review of mushrooms antiviral and immunomodulatory properties that may combat against COVID-19. Food Chem. Adv. 2022, 1, 100023.
    145. Jędrzejewski, T.; Pawlikowska, M.; Sobocińska, J.; Wrotek, S., COVID-19 and cancer diseases—The potential of Coriolus versicolor mushroom to combat global health challenges. Int. J. Mol. Sci. 2023, 24(5), 4864.
    146. Sharma, H. N.; Catrett, J.; Nwokeocha, O. D.; Boersma, M.; Miller, M. E.; Napier, A.; Robertson, B. K.; Abugri, D. A., Anti-Toxoplasma gondii activity of Trametes versicolor (Turkey tail) mushroom extract. Sci. Rep. 2023, 13(1), 8667.
    147. Dou, H.; Chang, Y.; Zhang, L., Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China. Prog. Mol. Biol. Transl. Sci. 2019, 163, 361-381.
    148. Standish, L. J.; Wenner, C. A.; Sweet, E. S.; Bridge, C.; Nelson, A.; Martzen, M.; Novack, J.; Torkelson, C., Trametes versicolor mushroom immune therapy in breast cancer. J. Soc. Integr. Oncol. 2008, 6(3), 122-128.
    149. Sekhon, B. K.; Sze, D. M. Y.; Chan, W. K.; Fan, K.; Li, G. Q.; Moore, D. E.; Roubin, R. H., PSP activates monocytes in resting human peripheral blood mononuclear cells: immunomodulatory implications for cancer treatment. Food Chem. 2013, 138(4), 2201-2209.
    150. Saleh, M. H.; Rashedi, I.; Keating, A., Immunomodulatory properties of Coriolus versicolor: the role of polysaccharopeptide. Front. Immunol. 2017, 8, 1087.
    151. Li, W.; Liu, M.; Lai, S.; Xu, C.; Lu, F.; Xiao, X.; Bao, Y., Immunomodulatory effects of polysaccharopeptide (PSP) in human PBMC through regulation of TRAF6/TLR immunosignal-transduction pathways. Immunopharmacol. Immunotoxicol. 2010, 32(4), 576-584.
    152. Wang, J.; Dong, B.; Tan, Y.; Yu, S.; Bao, Y. X., A study on the immunomodulation of polysaccharopeptide through the TLR4-TIRAP/MAL-MyD88 signaling pathway in PBMCs from breast cancer patients. Immunopharmacol. Immunotoxicol. 2013, 35(4), 497-504.
    153. Williams, L. M.; Berthon, B. S.; Stoodley, I. L.; Williams, E. J.; Wood, L. G., Medicinal mushroom extracts from Hericium coralloides and Trametes versicolor exert differential immunomodulatory effects on immune cells from older adults in vitro. Nutrients 2023, 15(9), 2227.
    154. Li, F.; Wen, H.; Zhang, Y.; An, M.; Liu, X., Purification and characterization of a novel immunomodulatory protein from the medicinal mushroom Trametes versicolor. Sci. China Life Sci. 2011, 54(4), 379-385.
    155. Yang, C. L. H.; Chik, S. C. C.; Lau, A. S. Y.; Chan, G. C. F., Coriolus versicolor and its bioactive molecule are potential immunomodulators against cancer cell metastasis via inactivation of MAPK pathway. J. Ethnopharmacol. 2023, 301, 115790.
    156. Hung, P. H.; Lin, C. M.; Tsai, J. C.; Hsu, T. H.; Chang, S. L.; Chen, Y. I.; Tzeng, C. Y., Acetylsalicylic acid-like analgesic effects of Trametes versicolor in Wistar rats. Biomed. Pharmacother. 2020, 129, 110328.
    157. Pallav, K.; Dowd, S. E.; Villafuerte, J.; Yang, X.; Kabbani, T.; Hansen, J.; Dennis, M.; Leffler, D. A.; Newburg, D. S.; Kelly, C. P., Effects of polysaccharopeptide from Trametes versicolor and amoxicillin on the gut microbiome of healthy volunteers: a randomized clinical trial. Gut Microbes 2014, 5(4), 458-467.
    158. Smith, H.; Doyle, S.; Murphy, R., Target directed identification of natural bioactive compounds from filamentous fungi. Food Chem. 2023, 405(pt.A), 134743.
    159. Bains, A.; Chawla, P., In vitro bioactivity, antimicrobial and anti-inflammatory efficacy of modified solvent evaporation assisted Trametes versicolor extract. 3 Biotech 2020, 10(9), 404.
    160. Roca-Lema, D.; Martinez-Iglesias, O.; Ana Portela, C. F.; Rodríguez-Blanco, A.; Valladares-Ayerbes, M.; Díaz-Díaz, A.; Casas-Pais, A.; Prego, C.; Figueroa, A., In vitro anti-proliferative and anti-invasive effect of polysaccharide-rich extracts from Trametes versicolor and Grifola frondosa in colon cancer cells. Int. J. Med. Sci. 2019, 16(2), 231-240.
    161. Ko, C. H.; Yue, G. G. L.; Gao, S.; Luo, K. W.; Siu, W. S.; Shum, W. T.; Shiu, H. T.; Lee, J. K. M.; Li, G.; Leung, P. C.; Evdokiou, A.; Lau, C. B. S., Evaluation of the combined use of metronomic zoledronic acid and Coriolus versicolor in intratibial breast cancer mouse model. J. Ethnopharmacol. 2017, 204, 77-85.
    162. Ricciardi, M. R.; Licchetta, R.; Mirabilii, S.; Scarpari, M.; Parroni, A.; Fabbri, A. A.; Cescutti, P.; Reverberi, M.; Fanelli, C.; Tafuri, A., Preclinical antileukemia activity of tramesan: a newly identified bioactive fungal metabolite. Oxid. Med. Cell. Longev. 2017, 2017, 5061639.
    163. Huang, Z.; Zhang, M.; Wang, Y.; Zhang, S.; Jiang, X., Extracellular and intracellular polysaccharide extracts of Trametes versicolor improve lipid profiles via serum regulation of lipid-regulating enzymes in hyperlipidemic mice. Curr. Microbiol. 2020, 77(11), 3526-3537.
    164. Wang, K. L.; Lu, Z. M.; Mao, X.; Chen, L.; Gong, J. S.; Ren, Y.; Geng, Y.; Li, H.; Xu, H. Y.; Xu, G. H.; Shi, J. S.; Xu, Z. H., Structural characterization and anti-alcoholic liver injury activity of a polysaccharide from Coriolus versicolor mycelia. Int. J. Biol. Macromol. 2019, 137, 1102-1111.
    165. Meng, F.; Lin, Y.; Hu, L.; Feng, W.; Su, P.; Wu, L., The therapeutic effect of Coriolus versicolor fruiting body on STZ-induced ICR diabetic mice. J. Healthc. Eng. 2022, 2022, 7282453.
    166. Lin, J.; He, Z.; Liu, S.; Polysaccharide peptide induced colorectal cancer cells apoptosis by down-regulating EGFR and PD-L1 expression. Iran. J. Pharm. Res. 2022, 21(1), e123909.
    167. Pilkington, K.; Wieland, L. S.; Teng, L.; Jin, X. Y.; Storey, D.; Liu, J. P., Coriolus (Trametes) versicolor mushroom to reduce adverse effects from chemotherapy or radiotherapy in people with colorectal cancer. Cochrane Database Syst. Rev. 2022, 11(11), CD012053.
    168. Shi, S.; Yin, L.; Shen, X.; Dai, Y.; Wang, J.; Yin, D.; Zhang, D.; Pan, X., β-Glucans from Trametes versicolor (L.) Lloyd is effective for prevention of influenza virus infection. Viruses 2022, 14(2), 237.
    169. Razmovski-Naumovski, V.; Kimble, B.; Laurenti, D.; Nammi, S.; Norimoto, H.; Chan, K., Polysaccharide peptide extract from Coriolus versicolor increased Tmax of tamoxifen and maintained biochemical serum parameters, with no change in the metabolism of tamoxifen in the rat. Front. Pharmacol. 2022, 13, 857864.
    170. Nikolic, M.; Lazarevic, N.; Novakovic, J.; Jeremic, N.; Jakovljevic, V.; Zivkovic, V.; Bradic, J.; Pecarski, D.; Tel-Çayan, G.; Glamocija, J.; Sokovic, M.; Gregori, A.; Petrovic, J., Characterization, in vitro biological activity and in vivo cardioprotective properties of Trametes versicolor (L.:Fr.) Quél. heteropolysaccharides in a rat model of metabolic syndrome. Pharmaceuticals 2023, 16(6), 787.
    171. Chen, H. L.; Chiang, H. C., Constituents of fruit bodies of Tramete orientalis. J. Chin. Chem. Soc. 1995, 42(1), 97-100.
    172. Rösecke, J.; Pietsch, M.; König, W. A., Volatile constituents of wood-rotting basidiomycetes. Phytochemistry 2000, 54(8), 747-750.
    173. Bian, X.; Bai, J.; Sun, K.; Huang, S.; Wang, K.; Tang, S.; Xue, C.; Hu, G.; Wu, X.; Hua, H.; Pei, Y., Trametramide A, a new pyridone alkaloid from the fungus Trametes trogii TGC-P-3. Magn. Reson. Chem. 2016, 54(9), 773-776.
    174. Habibi, E.; Sadat-Ebrahimi, S. E.; Mousazadeh, S. A.; Amanzadeh, Y., Mycochemical investigation of the turkey tail medicinal mushroom Trametes versicolor (higher basidiomycetes): a potential application of the isolated compounds in documented pharmacological studies. Int. J. Med. Mushrooms 2015, 17(3), 255-265.
    175. Borlagdan, M. S.; De Castro, M. E. G.; van Altena, I. A.; Ragasa, C. Y., Sterols from Trametes versicolor. Res. J. Pharm. Biol. Chem. Sci. 2017, 8(2), 740-744.
    176. Jin, M.; Zhou, W.; Jin, C.; Jiang, Z.; Diao, S.; Jin, Z.; Li, G., Anti-inflammatory activities of the chemical constituents isolated from Trametes versicolor. Nat. Prod. Res. 2019, 33(16), 2422-2425.
    177. Bi, C.; Guo, X. Y.; Che, Q. M., Chemical constituents from Coriolus versicolor L. J. Chin. Pharm. Sci. 2007, 16(1), 38-40.
    178. Qin, X. D.; Liu, J. K., Chemical constituents of Coriolus versicolor. J. Yunnan Agric. Univ. (Yunnan Nong Ye Da Xue Xue Bao, 云南农业大学学报) 2012, 27(5), 774-776.
    179. Kıvrak, I.; Kivrak, S.; Karababa, E., Assessment of bioactive compounds and antioxidant activity of Turkey tail medicinal mushroom Trametes versicolor (Agaricomycetes). Int. J. Med. Mushrooms 2020, 22(6), 559-571.
    180. Jinming, G.; Lin, H.; Jikai, L., A novel sterol from Chinese truffles Tuber indicum. Steroids 2001, 66(10), 771-775.
    181. Tran, T. T. T.; Dang, H. P.; Nguyen, T. N., Chemical constituents from methanolic extract of Solanum procumbens Lour (Solanaceae). Vietnam J. Sci. Technol. Eng. 2019, 61(3), 9-11.
    182. Kobori, M.; Yoshida, M.; Ohnishi-Kameyama, M.; Takei, T.; Shinmoto, H., 5α, 8α-epidioxy-22E-ergosta-6,9(11),22-trien-3β-ol from an edible mushroom suppresses growth of HL60 leukemia and HT29 colon adenocarcinoma cells. Biol. Pharm. Bull. 2006, 29(4), 755-759.
    183. Kawahara, N.; Sekita, S.; Satake, M., Steroids from Calvatia cyathiformis. Phytochemistry 1994, 37(1), 213-215.
    184. Liendo, A.; Visbal, G.; Piras, M. M.; Piras, R.; Urbina, J. A., Sterol composition and biosynthesis in Trypanosoma cruzi amastigotes. Mol. Biochem. Parasitol. 1999, 104(1), 81-91.
    185. Suttiarporn, P.; Chumpolsri, W.; Mahatheeranont, S.; Luangkamin, S.; Teepsawang, S.; Leardkamolkarn, V., Structures of phytosterols and triterpenoids with potential anti-cancer activity in bran of black non-glutinous rice. Nutrients 2015, 7(3), 1672-1687.
    186. Ukiya, M.; Akihisa, T.; Tokuda, H.; Hirano, M.; Oshikubo, M.; Nobukuni, Y.; Kimura, Y.; Tai, T.; Kondo, S.; Nishino, H., Inhibition of tumor-promoting effects by poricoic acids G and H and other lanostane-type triterpenes and cytotoxic activity of poricoic acids A and G from Poria cocos. J. Nat. Prod. 2002, 65, 462-465.
    187. Zhang, J.; Chen, B.; Liang, J.; Han, J.; Zhou, L.; Zhao, R.; Liu, H.; Dai, H., Lanostane triterpenoids with PTP1B inhibitory and glucose-uptake stimulatory activities from mushroom Fomitopsis pinicola collected in North America. J. Agric. Food Chem. 2020, 68, 10036-10049.
    188. Sofrenić, I.; Anđelković, B.; Todorović, N.; Stanojković, T.; Vujisić, L.; Novaković, M.; Milosavljević, S.; Tešević, V., Cytotoxic triterpenoids and triterpene sugar esters from the medicinal mushroom Fomitopsis betulina. Phytochemistry 2021, 181, 112580.
    189. Hung, D. X.; Kuo, P. C.; Tuan, N. N.; Trung, H. V.; Thanh, N. T.; Ha, N. T.; Giang, B. L.; Trung, N. Q.; Ngan, N. T.; Hai, H. V.; Phuong, D. L.; Quang, D. N.; Thang, T. D., Triterpenoids and steroids from the fruiting bodies of Hexagonia tenuis and their cytotoxicity. Nat. Prod. Res. 2021, 35, 251-256.
    190. Shao, H. J.; Qing, C.; Wang, F.; Zhang, Y. L.; Luo, D. Q.; Liu, J. K., A new cytotoxic lanostane triterpenoid from the basidiomycete Hebeloma versipelle. J. Antibiot. 2005, 58(12), 828-831.
    191. Huang, T. Z.; Du, D. Y.; Chen, Y. Q.; Yuan, B.; Ju, X. Y.; Feng, Y. J.; Wang, L.; Jiang, J. H., Chemical constituents and antitumor activity of fruiting body of Fomes fomentarius. Mycosystema 2012, 31(5), 775-783.
    192. Kobata, K.; Wada, T.; Hayashi, Y.; Shibata, H., Volemolide, a novel norsterol from the fungus Lactarius volemus. Biosci. Biotechnol. Biochem. 1994, 58(8), 1542-1544.
    193. Togashi, H.; Mizushina, Y.; Takemura, M.; Sugawara, F.; Koshino, H.; Esumi, Y.; Uzawa, J.; Kumagai, H.; Matsukage, A.; Yoshida, S.; Sakaguchi, K., 4-Hydroxy-17-methylincisterol, an inhibitor of DNA polymerase-α activity and the growth of human cancer cells in vitro. Biochem. Pharmacol. 1998, 56(5), 583-590.
    194. Mansoor, T. A.; Hong, J.; Lee, C. O.; Bae, S. J.; Im, K. S.; Jung, J. H., Cytotoxic sterol derivatives from a marine sponge Homaxinella sp. J. Nat. Prod. 2005, 68(3), 331-336.
    195. Huang, L.; Cao, Y.; Xu, H.; Chen, G., Separation and purification of ergosterol and stigmasterol in Anoectochilus roxburghii (wall) Lindl by high‐speed counter‐current chromatography. J. Sep. Sci. 2011, 34(4), 385-392.
    196. Anaya, J.; Caballero, M.; Grande, M.; Navarro, J. J.; Tapia, I.; Almeida, J. F., A lupeol derivative from Salvia pratensis. Phytochemistry 1989, 28(8), 2206-2208.
    197. Liu, H. K.; Tsai, T. H.; Chang, T. T.; Chou, C. J.; Lin, L. C., Lanostane-triterpenoids from the fungus Phellinus gilvus. Phytochemistry 2009, 70(4), 558-563.
    198. Lee, T. H.; Chiou, J. L.; Lee, C. K.; Kuo, Y. H., Separation and determination of chemical constituents in the roots of Rhus javanica L. var. roxburghiana. J. Chin. Chem. Soc. 2005, 52(4), 833-841.
    199. Ambrus, G.; Ilkőy, É.; Jekkel, A.; Horváth, G.; Böcskei, Z., Microbial transformation of β-sitosterol and stigmasterol into 26-oxygenated derivatives. Steroids 1995, 60(9), 621-625.
    200. Jo, B. S.; Cho, Y. J., Inhibitory activity against Helicobacter pylori of isolated compounds from Pinus koraiensis Siebold et Zucc Leaves. J. Appl. Biol. Chem. 2016, 59(1), 19-23.
    201. Chen, C. Y.; Chang, F. R.; Teng, C. M.; Wu, Y. C., Cheritamine, a new N-fatty tryptamine and other constituents from the stems of Annona cherimola. J. Chin. Chem. Soc. 1999, 46(1), 77-86.
    202. Aissa, I.; Sghair, R. M.; Bouaziz, M.; Laouini, D.; Sayadi, S.; Gargouri, Y., Synthesis of lipophilic tyrosyl esters derivatives and assessment of their antimicrobial and antileishmania activities. Lipids Health Dis. 2012, 11, 1-8.
    203. Chung, C. P.; Hsia, S. M.; Lee, M. Y.; Chen, H. J.; Cheng, F.; Chan, L. C.; Kuo, Y. H.; Lin, Y. L.; Chiang, W., Gastroprotective activities of adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) on the growth of the stomach cancer AGS cell line and indomethacin-induced gastric ulcers. J. Agric. Food Chem. 2011, 59(11), 6025-6033.
    204. Dang, N. Q.; Dang, D. B., Ergosta-4,6,8(14), 22-tetraen-3-one from Vietnamese Xylaria sp. possessing inhibitory activity of nitric oxide production. Nat. Prod. Res. 2008, 22(10), 901-906.
    205. Shin, M. K.; Sasaki, F.; Ki, D. W.; Win, N. N.; Morita, H.; Hayakawa, Y., Anti-metastatic effects of ergosterol peroxide from the entomopathogenic fungus Ophiocordyceps gracilioides on 4T1 breast cancer cells. J. Nat. Med. 2021, 75(4), 824-832.
    206. Kang, J. H.; Jang, J. E.; Mishra, S. K.; Lee, H. J.; Nho, C. W.; Shin, D.; Jin, M.; Kim, M. K.; Choi, C.; Oh, S. H., Ergosterol peroxide from Chaga mushroom (Inonotus obliquus) exhibits anti-cancer activity by down-regulation of the β-catenin pathway in colorectal cancer. J. Ethnopharmacol. 2015, 173, 303-312.
    207. Lu, H.; Zou, W. X.; Meng, J. C.; Hu, J.; Tan, R. X., New bioactive metabolites produced by Colletotrichum sp., an endophytic fungus in Artemisia annua. Plant Sci. 2000, 151(1), 67-73.
    208. Keyzers, R. A.; Davies-Coleman, M. T., Anti-inflammatory metabolites from marine sponges. Chem. Soc. Rev. 2005, 34(4), 355-365.
    209. Liaw, C. C.; Wu, S. J.; Chen, C. F.; Lai, M. N.; Ng, L. T., Anti-inflammatory activity and bioactive constituents of cultivated fruiting bodies of Xylaria nigripes (ascomycetes), a chinese medicinal fungus. Int. J. Med. Mushrooms 2017, 19(10), 915-924.
    210. Pereira, D. M.; Correia-da-Silva, G.; Valentão, P.; Teixeira, N.; Andrade, P. B., Anti-inflammatory effect of unsaturated fatty acids and ergosta-7,22-dien-3-ol from Marthasterias glacialis: prevention of CHOP-mediated ER-stress and NF-κB activation. PLoS ONE 2014, 9(2), e88341.
    211. Lone, S. H.; Bhat, K. A; Khuroo, M. A., Phytochemical analysis and chemobiological standardization of Artemisia amygdalina. Chem. Pharmacol. Perspect. Artemisia amygdalina 2015, 25-37.
    212. Seo, H. W.; Hung, T. M.; Na, M.; Jung, H. J.; Kim, J. C.; Choi, J. S.; Kim, J. H.; Lee, H. K.; Lee, I. S.; Bae, K. H.; Hattori, M.; Min, B. S., Steroids and triterpenes from the fruit bodies of Ganoderma lucidum and their anti-complement activity. Arch. Pharmacal Res. 2009, 32, 1573-1579.
    213. Mayaka, R. K.; Njue, A. W.; Langat, M. K.; Cheplogoi, P. K.; Omolo, J. O., Antimicrobial compounds from the Kenyan Ganoderma adspersum (Schulz.) Donk species. Int. J. Biol. Chem. Sci. 2019, 13(7), 3390-3397.
    214. Hung, D. X.; Kuo, P. C.; Tuan, N. N.; Trung, H. V.; Thanh, N. T.; Ha, N. T.; Giang, B. L.; Trung, N. Q.; Ngan, N. T.; Hai, H. V.; Phuong, D. L.; Quang, D. N.; Thang, T. D., Triterpenoids and steroids from the fruiting bodies of Hexagonia tenuis and their cytotoxicity. Nat. Prod. Res. 2021, 35(2), 251-256.
    215. Russo, A.; Cardile, V.; Piovano, M.; Caggia, S.; Espinoza, C. L.; Garbarino, J. A., Pro-apoptotic activity of ergosterol peroxide and (22E)-ergosta-7,22-dien-5α-hydroxy-3,6-dione in human prostate cancer cells. Chem. Biol. Interact. 2010, 184, 352-358.
    216. Ling, T.; Lang, W. H.; Martinez-Montemayor, M. M.; Rivas, F., Development of ergosterol peroxide probes for cellular localisation studies. Org. Biomol. Chem. 2019, 17, 5223-5229.
    217. Akihisa, T.; Nakamura, Y.; Tagata, M.; Tokuda, H.; Yasukawa, K.; Uchiyama, E.; Suzuki, T.; Kimura, Y., Anti‐inflammatory and anti‐tumor‐promoting effects of triterpene acids and sterols from the fungus Ganoderma lucidum. Chem. Biodivers. 2007, 4(2), 224-231.
    218. Chen, C.; Liang, F.; Chen, B.; Sun, Z.; Xue, T.; Yang, R.; Luo, D., Identification of demethylincisterol A3 as a selective inhibitor of protein tyrosine phosphatase Shp2. Eur. J. Pharmacol. 2017, 795, 124-133.
    219. Zhou, J.; Li, G.; Deng, Q.; Zheng, D.; Yang, X.; Xu, J., Cytotoxic constituents from the mangrove endophytic Pestalotiopsis sp. induce G0/G1 cell cycle arrest and apoptosis in human cancer cells. Nat. Prod. Res. 2018, 32(24), 2968-2972.
    220. Sun, M.; Zhou, D.; Wu, J.; Zhou, J.; Xu, J., Sdy-1 executes antitumor activity in HepG2 and HeLa cancer cells by inhibiting the Wnt/β-catenin signaling pathway. Mar. Drugs 2022, 20(2), 125.

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