LACTB is a tumour suppressor that modulates lipid metabolism and cell state

被引:0
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作者
Zuzana Keckesova
Joana Liu Donaher
Jasmine De Cock
Elizaveta Freinkman
Susanne Lingrell
Daniel A. Bachovchin
Brian Bierie
Verena Tischler
Aurelia Noske
Marian C. Okondo
Ferenc Reinhardt
Prathapan Thiru
Todd R. Golub
Jean E. Vance
Robert A. Weinberg
机构
[1] Whitehead Institute for Biomedical Research,Department of Medicine and the Group on Molecular and Cell Biology of Lipids
[2] University of Alberta,Department of Biology
[3] Broad Institute,undefined
[4] Massachusetts Institute of Technology,undefined
[5] Chemical Biology Program,undefined
[6] Memorial Sloan Kettering Cancer Center,undefined
[7] Institute of Surgical Pathology,undefined
[8] University Hospital Zurich,undefined
[9] Massachusetts Institute of Technology,undefined
[10] MIT Ludwig Center for Molecular Oncology,undefined
[11] Massachusetts Institute of Technology,undefined
[12] Metabolon,undefined
[13] Inc.,undefined
来源
Nature | 2017年 / 543卷
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摘要
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.
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页码:681 / 686
页数:5
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