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MYC、细胞竞争与癌症中的细胞死亡:不可分割的三联体

MYC, Cell Competition, and Cell Death in Cancer: The Inseparable Triad.

作者信息

Di Giacomo Simone, Sollazzo Manuela, Paglia Simona, Grifoni Daniela

机构信息

Department of Pharmacy and Biotechnology, University of Bologna, Via Selmi 3, 40126 Bologna, Italy.

出版信息

Genes (Basel). 2017 Apr 17;8(4):120. doi: 10.3390/genes8040120.

Abstract

Deregulation of MYC family proteins in cancer is associated with a global reprogramming of gene expression, ultimately promoting glycolytic pathways, cell growth, and proliferation. It is well known that MYC upregulation triggers cell-autonomous apoptosis in normal tissues, while frankly malignant cells develop resistance to apoptotic stimuli, partly resulting from MYC addiction. As well as inducing cell-autonomous apoptosis, MYC upregulation is able to trigger non cell-autonomous apoptotic death through an evolutionarily conserved mechanism known as "cell competition". With regard to this intimate and dual relationship between MYC and cell death, recent evidence obtained in models of cancer has revealed that, in early tumourigenesis, MYC upregulation guides the clonal expansion of mutant cells, while the surrounding tissue undergoes non-cell autonomous death. Apoptosis inhibition in this context was shown to restrain tumour growth and to restore a wild-type phenotype. This suggests that cell-autonomous and non cell-autonomous apoptosis dependent on MYC upregulation may shape tumour growth in different ways, soliciting the need to reconsider the role of cell death in cancer in the light of this new level of complexity. Here we review recent literature about MYC and cell competition obtained in , with a particular emphasis on the relevance of cell death to cell competition and, more generally, to cancer. Possible implications of these findings for the understanding of mammalian cancers are also discussed.

摘要

癌症中MYC家族蛋白的失调与基因表达的全面重编程相关,最终促进糖酵解途径、细胞生长和增殖。众所周知,MYC上调会在正常组织中引发细胞自主性凋亡,而恶性细胞对凋亡刺激产生抗性,部分原因是对MYC成瘾。除了诱导细胞自主性凋亡外,MYC上调还能够通过一种称为“细胞竞争”的进化保守机制引发非细胞自主性凋亡死亡。关于MYC与细胞死亡之间这种密切的双重关系,最近在癌症模型中获得的证据表明,在早期肿瘤发生过程中,MYC上调引导突变细胞的克隆扩增,而周围组织则经历非细胞自主性死亡。在这种情况下,凋亡抑制被证明可以抑制肿瘤生长并恢复野生型表型。这表明依赖于MYC上调的细胞自主性和非细胞自主性凋亡可能以不同方式塑造肿瘤生长,促使我们需要根据这种新的复杂程度重新考虑细胞死亡在癌症中的作用。在这里,我们回顾了最近在[具体模型]中获得的关于MYC和细胞竞争的文献,特别强调细胞死亡与细胞竞争以及更广泛地与癌症的相关性。还讨论了这些发现对理解哺乳动物癌症的可能影响。

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