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Article

Patient-Derived Tumor Chemosensitization of GKB202, an Antrodia Cinnamomea Mycelium-Derived Bioactive Compound

1
Biotech Research Institute, Grape King Bio, Taoyuan 32542, Taiwan
2
CancerFree Biotech Ltd., Taipei City 106, Taiwan
3
Department of Radiation Oncology, Taipei Medical University Hospital, Taipei City 110, Taiwan
4
TMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei City 110, Taiwan
5
Department of Radiology, School of Medicine, College of Medicine, Taipei Medical University, Taipei City 110, Taiwan
6
Graduate Institute of Biomedical Materials and Tissue Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei City 110, Taiwan
7
International Ph.D. Program in Biomedical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei City 110, Taiwan
8
International Ph.D. Program for Cell Therapy and Regenerative Medicine, College of Medicine, Taipei Medical University, Taipei City 11031, Taiwan
9
Department of Food Science, Nutrition, and Nutraceutical Biotechnology, Shih Chien University, Taipei City 104, Taiwan
10
Institute of Food Science and Technology, National Taiwan University, Taipei City 10617, Taiwan
*
Authors to whom correspondence should be addressed.
Molecules 2021, 26(19), 6018; https://doi.org/10.3390/molecules26196018
Submission received: 18 August 2021 / Revised: 29 September 2021 / Accepted: 29 September 2021 / Published: 4 October 2021
(This article belongs to the Special Issue Bioactive Compounds from Nature: New Research and Prospects)

Abstract

Oral cancers, hepatocellular carcinoma, and colorectal cancers are the three most common cancers, leading to 18,000 cases of cancer-related mortality in Taiwan per year. To bridge the gap towards clinical translation, we developed a circulating tumor cell (CTC) organoid culture workflow that efficiently expands CTC from patients to test Antrodia Cinnamomea mycelium-derived bioactive compounds. Three ACM-derived bioactive compounds were evaluated for tumor chemosensitization characteristics. Significant and consistent cytotoxic/5-FU sensitizing effects of GKB202 were found on 8 different patient-derived tumors. Acute toxicity profile and hepatic metabolism of GKB202 in rats suggest GKB202 is rapidly cleared by liver and is well tolerated up to the dose of 20 mg/kg. This comprehensive study provides new evidence that liquid fermentation of Antrodia cinnamomea mycelium (ACM) contains bioactive compounds that lead to effective control of CTC, especially when combined with 5-FU. Together, these data suggest ACM-derived GKB202 may be considered for further clinical investigation in the context of 5-FU-based combination therapy.
Keywords: Antrodia Cinnamomea mycelium; ACM; circulating tumor cells; patient-derived organoid; 5-FU Antrodia Cinnamomea mycelium; ACM; circulating tumor cells; patient-derived organoid; 5-FU

Share and Cite

MDPI and ACS Style

Li, T.-J.; Lin, T.-W.; Wu, S.-P.; Chu, H.-T.; Kuo, Y.-H.; Chiou, J.-F.; Lu, L.-S.; Chen, C.-C. Patient-Derived Tumor Chemosensitization of GKB202, an Antrodia Cinnamomea Mycelium-Derived Bioactive Compound. Molecules 2021, 26, 6018. https://doi.org/10.3390/molecules26196018

AMA Style

Li T-J, Lin T-W, Wu S-P, Chu H-T, Kuo Y-H, Chiou J-F, Lu L-S, Chen C-C. Patient-Derived Tumor Chemosensitization of GKB202, an Antrodia Cinnamomea Mycelium-Derived Bioactive Compound. Molecules. 2021; 26(19):6018. https://doi.org/10.3390/molecules26196018

Chicago/Turabian Style

Li, Tsung-Ju, Ting-Wei Lin, Shih-Pei Wu, Hsin-Tung Chu, Yu-Hsuan Kuo, Jeng-Fong Chiou, Long-Sheng Lu, and Chin-Chu Chen. 2021. "Patient-Derived Tumor Chemosensitization of GKB202, an Antrodia Cinnamomea Mycelium-Derived Bioactive Compound" Molecules 26, no. 19: 6018. https://doi.org/10.3390/molecules26196018

APA Style

Li, T.-J., Lin, T.-W., Wu, S.-P., Chu, H.-T., Kuo, Y.-H., Chiou, J.-F., Lu, L.-S., & Chen, C.-C. (2021). Patient-Derived Tumor Chemosensitization of GKB202, an Antrodia Cinnamomea Mycelium-Derived Bioactive Compound. Molecules, 26(19), 6018. https://doi.org/10.3390/molecules26196018

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