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LACTB是一种调节脂质代谢和细胞状态的肿瘤抑制因子。

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

作者信息

Keckesova Zuzana, Donaher Joana Liu, De Cock Jasmine, Freinkman Elizaveta, Lingrell Susanne, Bachovchin Daniel A, Bierie Brian, Tischler Verena, Noske Aurelia, Okondo Marian C, Reinhardt Ferenc, Thiru Prathapan, Golub Todd R, Vance Jean E, Weinberg Robert A

机构信息

Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA.

Metabolon, Inc., PO Box 110407, Research Triangle Park, North Carolina 27709, USA.

出版信息

Nature. 2017 Mar 30;543(7647):681-686. doi: 10.1038/nature21408. Epub 2017 Mar 22.

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.

摘要

有丝分裂后的分化细胞表现出多种与活跃生长的肿瘤细胞不同的特征,如细胞周期抑制剂和分化因子的表达。我们推测这些分化细胞的基因表达谱可能揭示出可能作为肿瘤抑制因子发挥作用的基因的身份。在这里,我们通过对小鼠和人类的体外和体内研究表明,线粒体蛋白LACTB能有效抑制乳腺癌细胞的增殖。其作用机制涉及线粒体脂质代谢的改变和乳腺癌细胞的分化。这至少部分是通过降低参与线粒体磷脂酰乙醇胺合成的线粒体磷脂丝氨酸脱羧酶的水平来实现的。这些观察结果揭示了一种新的线粒体肿瘤抑制因子,并证明了线粒体脂质代谢与乳腺癌细胞分化程序之间的联系,从而揭示了一种以前未描述的肿瘤抑制机制。

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