| Literature DB >> 33431809 |
Emilie Jaune1,2,3, Elisa Cavazza1,2,3, Cyril Ronco3,4, Oleksandr Grytsai3,4, Patricia Abbe1,2,3, Nedra Tekaya1,2,3, Marwa Zerhouni1,2,3, Guillaume Beranger1,2,3, Lisa Kaminski3,5, Frédéric Bost3,5, Maeva Gesson1,2,3, Meri Tulic1,2,3, Paul Hofman6,7,8, Robert Ballotti3,9, Thierry Passeron1,2,10, Thomas Botton11,12,13, Rachid Benhida14,15, Stéphane Rocchi16,17,18.
Abstract
In the search of biguanide-derived molecules against melanoma, we have discovered and developed a series of bioactive products and identified the promising new compound CRO15. This molecule exerted anti-melanoma effects on cells lines and cells isolated from patients including the ones derived from tumors resistant to BRAF inhibitors. Moreover, CRO15 was able to decrease viability of cells lines from a broad range of cancer types. This compound acts by two distinct mechanisms. First by activating the AMPK pathway induced by a mitochondrial disorder. Second by inhibition of MELK kinase activity, which induces cell cycle arrest and activation of DNA damage repair pathways by p53 and REDD1 activation. All of these mechanisms activate autophagic and apoptotic processes resulting in melanoma cell death. The strong efficacy of CRO15 to reduce the growth of melanoma xenograft sensitive or resistant to BRAF inhibitors opens interesting perspective.Entities:
Year: 2021 PMID: 33431809 PMCID: PMC7801734 DOI: 10.1038/s41419-020-03344-6
Source DB: PubMed Journal: Cell Death Dis Impact factor: 8.469