4.6 Article

A combined treatment with melatonin and andrographis promotes autophagy and anticancer activity in colorectal cancer

期刊

CARCINOGENESIS
卷 43, 期 3, 页码 217-230

出版社

OXFORD UNIV PRESS
DOI: 10.1093/carcin/bgac008

关键词

-

类别

资金

  1. National Cancer Institute, National Institutes of Health [CA184792, CA187956, CA227602, CA072851, CA202797]

向作者/读者索取更多资源

Melatonin and andrographis were found to have a synergistic therapeutic effect in the treatment of colorectal cancer (CRC) by inducing autophagy-associated pathways and apoptotic activation. This combination therapy shows promise as a potential treatment option for CRC patients.
We systematically used multiple in vitroand in vivomodels to demonstrate melatonin and andrographis exhibit pronounced synergistic activity in CRC inhibition, mediated in part by autophagy-associated pathways induced apoptotic activation, highlighting the combinatorial therapeutic potential of these two natural products in patients with CRC. Colorectal cancer (CRC) is one of the most frequent malignancies worldwide and remains one of the leading causes of cancer-related deaths in the USA. The high degree of morbidity and mortality associated with this disease is largely due to the inadequate efficacy of current treatments as well the development of chemoresistance. In recent years, several pharmaceutical agents screened from natural products have shown the promise to offer a safe, inexpensive and synergistically multi-targeted treatment option in various cancers. Given the growing evidence of anti-carcinogenic properties of two natural compounds, melatonin (MLT) and andrographis (Andro), we aimed to evaluate their synergistic anticancer effects in CRC. We demonstrate that indeed these two compounds possessed a synergistic anticancer effect in terms of their ability to inhibit cell viability, suppression of colony-formation and induction of apoptosis (P < 0.05). In line with our in vitro findings, we were able to validate this combinatorial anticancer activity in xenograft animal models (P < 0.001) as well as tumor-derived 3D organoids (P < 0.01). RNA-sequencing analysis revealed candidate pathways and genes that mediated antitumor efficacy of MLT and Andro in CRC, among which autophagy pathway and related genes, including NR4A1, CTSL and Atg12, were found to be primarily responsible for the increased anticancer effect by the two natural products. In conclusion, our data reveal a potent and synergistic therapeutic effect of MLT and Andro in the treatment of CRC and provides a rationale for suppressing autophagy in cancer cells as a potential therapeutic strategy for CRC.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据