4.6 Article

Anticancer Activity of 2-O-caffeoyl Alphitolic Acid Extracted from the Lichen, Usnea barbata 2017-KL-10

期刊

MOLECULES
卷 26, 期 13, 页码 -

出版社

MDPI
DOI: 10.3390/molecules26133937

关键词

colorectal cancer; 2-O-caffeoyl alphitolic acid; lichen; Usnea barbata; apoptosis; HCT116

资金

  1. National Research Foundation of Korea (NFR) - Korea government (MSIT) [NRF-2018R1C1B5085764, NRF-2020R1A6A1A03044512, NRF-2021R1A2C1010727]

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Colorectal cancer is a life-threatening disease with poor prognosis for metastatic patients. Lichens have been identified as sources of bioactive metabolites, including anticancer properties. The study evaluated the anticancer effect of a lichen-derived metabolite, 2OCAA, on colorectal cancer cells, demonstrating its potential as a therapeutic candidate.
Colorectal cancer is one of the life-threatening ailments causing high mortality and morbidity worldwide. Despite the innovation in medical genetics, the prognosis for metastatic colorectal cancer in patients remains unsatisfactory. Recently, lichens have attracted the attention of researchers in the search for targets to fight against cancer. Lichens are considered mines of thousands of metabolites. Researchers have reported that lichen-derived metabolites demonstrated biological effects, such as anticancer, antiviral, anti-inflammatory, antibacterial, analgesic, antipyretic, antiproliferative, and cytotoxic, on various cell lines. However, the exploration of the biological activities of lichens' metabolites is limited. Thus, the main objective of our study was to evaluate the anticancer effect of secondary metabolites isolated from lichen (Usnea barbata 2017-KL-10) on the human colorectal cancer cell line HCT116. In this study, 2OCAA exhibited concentration-dependent anticancer activities by suppressing antiapoptotic genes, such as MCL-1, and inducing apoptotic genes, such as BAX, TP53, and CDKN1A(p21). Moreover, 2OCAA inhibited the migration and invasion of colorectal cancer cells in a concentration-dependent manner. Taken together, these data suggest that 2OCAA is a better therapeutic candidate for colorectal cancer.

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