Compound K: A systematic review of its anticancer properties and probable mechanisms

Author:

Tam Dao Ngoc Hien12,Nam Nguyen Hai23,Cuong Nguyen The Ky24,Hung Dang The25,Soa Dang Thi26,Altom Ahmad27,Tran Linh89,Elhadad Heba210,Huy Nguyen Tien211ORCID

Affiliation:

1. Asia Shine Trading & Service Co., Ltd. Ho Chi Minh City 700000 Vietnam

2. Online Research Club (https://www.onlineresearchclub.org/) Nagasaki Japan

3. Division of Hepato‐Biliary‐Pancreatic Surgery and Transplantation, Department of Surgery, Graduate School of Medicine Kyoto University Kyoto Japan

4. Oncology Department Thu Duc City Hospital Ho Chi Minh City 700000 Vietnam

5. Faculty of Medicine University of Medicine and Pharmacy Ho Chi Minh City Ho Chi Minh City 700000 Vietnam

6. Faculty of Pharmacy Vinh Medical University Nghe An 43000‐44000 Vietnam

7. Department of Internal Medicine, Faculty of Medicine Damascus University Damascus Syrian Arab Republic

8. Institute of Fundamental and Applied Sciences Duy Tan University Ho Chi Minh City 700000 Vietnam

9. Faculty of Natural Sciences Duy Tan University Da Nang City 550000 Vietnam

10. Department of Parasitology, Medical Research Institute Alexandria University Alexandria Egypt

11. School of Tropical Medicine and Global Health (TMGH) Nagasaki University 1‐12‐4 Sakamoto Nagasaki 852‐8523 Japan

Abstract

AbstractPanax ginseng is a common natural product, which is well‐known to have a wide range of pharmacological activities in cancer. Its metabolite, compound K (CK), has been reported to have anticancer activity. We aimed to systematically review the literature for evidence of anticancer effects of CK. We conducted a systematic search in eight databases. We included all in vitro and in vivo studies investigating the anticancer effects of CK with no restrictions. Quality assessment was applied by ToxRTool. Fifty‐four articles were included in our study. The purity of CK in our included studies was at least 95%. The in vitro studies reported that CK had a potential anticancer activity on several cell lines including human lung cancer cell lines (A549, PC‐9), nasopharyngeal carcinoma cell line (Hk‐1), liver cancer cell line (BEL 7402), and pediatric acute myeloid leukemia cell lines (Kasumi‐1, MV4‐11). The in vivo studies reported a significant decrease in tumor volume in mice treated with CK. CK is a potential supplementary treatment in cancer chemotherapies. The safety and further clinical trials of CK should be explored for future drug development.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference89 articles.

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