| Literature DB >> 33592379 |
Wenli Shi1, Danyi Lu2, Chunlei Wu3, Meiqing Li4, Zhihao Ding3, Yanyan Li4, Binghua Chen4, Xian Lin3, Wu Su3, Ximing Shao3, Zhihui Xia5, Lijing Fang6, Ke Liu7, Hongchang Li8.
Abstract
Natural products are useful tools for biological mechanism research and drug discovery. Due to the excellent tumor cell growth inhibitory profile and sub-nanomolar potency, Coibamide A (CA), an N-methyl-stabilized depsipeptide isolated from marine cyanobacterium, has been considered as a promising lead compound for cancer treatment. However, the molecular anti-cancer mechanism of the action of CA remains unclear. Here, we showed that CA treatment induced caspase-independent cell death in breast cancer cells. CA treatment also led to severe lysosome defects, which was ascribed to the impaired glycosylation of lysosome membrane protein LAMP1 and LAMP2. As a consequence, the autophagosome-lysosome fusion was blocked upon CA treatment. In addition, we presented evidence that this autophagy defect partially contributed to the CA treatment-induced tumor cell death. Together, our work uncovers a novel mechanism underlying the anti-cancer action of CA, which will promote its further application for cancer therapy.Entities:
Keywords: Autophagy mediated cell death; Coibamide a; LAMP protein Glycosylation
Year: 2021 PMID: 33592379 DOI: 10.1016/j.bbrc.2021.01.112
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575