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蛋氨酸限制通过癌基因Src 打破细胞增殖和死亡的强制性偶联。

Methionine restriction breaks obligatory coupling of cell proliferation and death by an oncogene Src in .

机构信息

Division of Cell Physiology, Kobe University, Kobe, Japan.

RIKEN CPR, Kobe, Japan.

出版信息

Elife. 2021 Apr 27;10:e59809. doi: 10.7554/eLife.59809.

Abstract

Oncogenes often promote cell death as well as proliferation. How oncogenes drive these diametrically opposed phenomena remains to be solved. A key question is whether cell death occurs as a response to aberrant proliferation signals or through a proliferation-independent mechanism. Here, we reveal that Src, the first identified oncogene, simultaneously drives cell proliferation and death in an obligatorily coupled manner through parallel MAPK pathways. The two MAPK pathways diverge from a lynchpin protein Slpr. A MAPK p38 drives proliferation whereas another MAPK JNK drives apoptosis independently of proliferation signals. Src-p38-induced proliferation is regulated by methionine-mediated Tor signaling. Reduction of dietary methionine uncouples the obligatory coupling of cell proliferation and death, suppressing tumorigenesis and tumor-induced lethality. Our findings provide an insight into how cells evolved to have a fail-safe mechanism that thwarts tumorigenesis by the oncogene Src. We also exemplify a diet-based approach to circumvent oncogenesis by exploiting the fail-safe mechanism.

摘要

癌基因通常既促进细胞增殖又促进细胞死亡。癌基因如何驱动这两种截然相反的现象仍有待解决。一个关键问题是,细胞死亡是作为对异常增殖信号的反应发生的,还是通过增殖独立的机制发生的。在这里,我们揭示了第一个被确定的癌基因Src 以一种强制性偶联的方式通过平行的 MAPK 途径同时驱动细胞增殖和死亡。两条 MAPK 途径从一个关键蛋白 Slpr 分叉。MAPK p38 驱动增殖,而另一条 MAPK JNK 则独立于增殖信号驱动细胞凋亡。Src-p38 诱导的增殖受蛋氨酸介导的 Tor 信号调节。减少饮食中的蛋氨酸会打破细胞增殖和死亡的强制性偶联,从而抑制肿瘤发生和肿瘤诱导的致死性。我们的发现提供了一个深入了解细胞如何进化出一种失效保护机制的视角,该机制通过癌基因 Src 阻止肿瘤发生。我们还通过利用失效保护机制,举例说明了一种基于饮食的方法来规避致癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/715d/8079150/3c39227ae69d/elife-59809-fig1.jpg

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