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MYC 拨动生物钟:MYC 与癌症中分子生物钟的复杂相互作用。

MYC Ran Up the Clock: The Complex Interplay between MYC and the Molecular Circadian Clock in Cancer.

机构信息

Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.

Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.

出版信息

Int J Mol Sci. 2021 Jul 20;22(14):7761. doi: 10.3390/ijms22147761.

Abstract

The MYC oncoprotein and its family members N-MYC and L-MYC are known to drive a wide variety of human cancers. Emerging evidence suggests that MYC has a bi-directional relationship with the molecular clock in cancer. The molecular clock is responsible for circadian (~24 h) rhythms in most eukaryotic cells and organisms, as a mechanism to adapt to light/dark cycles. Disruption of human circadian rhythms, such as through shift work, may serve as a risk factor for cancer, but connections with oncogenic drivers such as MYC were previously not well understood. In this review, we examine recent evidence that MYC in cancer cells can disrupt the molecular clock; and conversely, that molecular clock disruption in cancer can deregulate and elevate MYC. Since MYC and the molecular clock control many of the same processes, we then consider competition between MYC and the molecular clock in several select aspects of tumor biology, including chromatin state, global transcriptional profile, metabolic rewiring, and immune infiltrate in the tumor. Finally, we discuss how the molecular clock can be monitored or diagnosed in human tumors, and how MYC inhibition could potentially restore molecular clock function. Further study of the relationship between the molecular clock and MYC in cancer may reveal previously unsuspected vulnerabilities which could lead to new treatment strategies.

摘要

MYC 癌蛋白及其家族成员 N-MYC 和 L-MYC 已知可驱动多种人类癌症。新出现的证据表明,MYC 与癌症中的分子钟之间存在双向关系。分子钟负责大多数真核细胞和生物体的昼夜节律(约 24 小时),是一种适应光/暗循环的机制。人类昼夜节律的破坏,例如通过轮班工作,可能是癌症的一个风险因素,但与 MYC 等致癌驱动因素的联系以前并不清楚。在这篇综述中,我们检查了最近的证据,表明癌细胞中的 MYC 可以破坏分子钟;相反,癌症中的分子钟破坏会使 MYC 失调和升高。由于 MYC 和分子钟控制着许多相同的过程,因此我们考虑了 MYC 和分子钟在肿瘤生物学的几个特定方面(包括染色质状态、全局转录谱、代谢重编程和肿瘤中的免疫浸润)之间的竞争。最后,我们讨论了如何在人类肿瘤中监测或诊断分子钟,以及 MYC 抑制如何可能恢复分子钟功能。进一步研究癌症中分子钟和 MYC 之间的关系可能会揭示以前未被怀疑的弱点,从而为新的治疗策略提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d64/8305799/d67d4a84037e/ijms-22-07761-g001.jpg

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