| Literature DB >> 28329758 |
Zuzana Keckesova1, Joana Liu Donaher1, Jasmine De Cock1, Elizaveta Freinkman1,2, Susanne Lingrell3, Daniel A Bachovchin4,5, Brian Bierie1, Verena Tischler6, Aurelia Noske6, Marian C Okondo5, Ferenc Reinhardt1, Prathapan Thiru1, Todd R Golub4, Jean E Vance3, Robert A Weinberg1,7,8.
Abstract
Post-mitotic, differentiated cells exhibit a variety of characteristics that contrast with those of actively growing neoplastic cells, such as the expression of cell-cycle inhibitors and differentiation factors. We hypothesized that the gene expression profiles of these differentiated cells could reveal the identities of genes that may function as tumour suppressors. Here we show, using in vitro and in vivo studies in mice and humans, that the mitochondrial protein LACTB potently inhibits the proliferation of breast cancer cells. Its mechanism of action involves alteration of mitochondrial lipid metabolism and differentiation of breast cancer cells. This is achieved, at least in part, through reduction of the levels of mitochondrial phosphatidylserine decarboxylase, which is involved in the synthesis of mitochondrial phosphatidylethanolamine. These observations uncover a novel mitochondrial tumour suppressor and demonstrate a connection between mitochondrial lipid metabolism and the differentiation program of breast cancer cells, thereby revealing a previously undescribed mechanism of tumour suppression.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28329758 PMCID: PMC6246920 DOI: 10.1038/nature21408
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962