MYC leads the way.

Q2 Biochemistry, Genetics and Molecular Biology
Small GTPases Pub Date : 2020-03-01 Epub Date: 2017-11-25 DOI:10.1080/21541248.2017.1364821
Niranjan Venkateswaran, Maralice Conacci-Sorrell
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引用次数: 25

Abstract

Members of the MYC family of proto-oncogenes are the most commonly deregulated genes in all human cancers. MYC proteins drive an increase in cellular proliferation and facilitate multiple aspects of tumor initiation and progression, thereby controlling all hallmarks of cancer. MYC's ability to drive metabolic reprogramming of tumor cells leading to biomass accumulation and cellular proliferation is the most studied function of these oncogenes. MYC also regulates tumor progression and is often implicated in resistance to chemotherapy and in metastasis. While most oncogenic functions of MYC are attributed to its role as a transcription factor, more recently, new roles of MYC as a pro-survival factor in the cytoplasm suggest a previously unappreciated diversity in MYC's roles in cancer progression. This review will focus on the role of MYC in invasion and will discuss the canonical functions of MYC in Epithelial to Mesenchymal Transition and the cytoplasmic functions of MYC-nick in collective migration.

MYC引领潮流。
MYC原癌基因家族的成员是所有人类癌症中最常见的不受调控的基因。MYC蛋白驱动细胞增殖增加,促进肿瘤发生和进展的多个方面,从而控制癌症的所有特征。MYC驱动肿瘤细胞代谢重编程导致生物量积累和细胞增殖的能力是这些癌基因研究最多的功能。MYC还调节肿瘤进展,并经常与化疗耐药和转移有关。虽然MYC的大多数致癌功能归因于其作为转录因子的作用,但最近,MYC作为细胞质中促生存因子的新作用表明,MYC在癌症进展中的作用存在以前未被认识到的多样性。本文将重点讨论MYC在侵袭中的作用,并讨论MYC在上皮细胞向间质细胞转化中的典型功能以及MYC-nick在集体迁移中的细胞质功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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