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KIAA1524/CIP2A通过协调mTORC1和MYC的活性促进癌症生长。

KIAA1524/CIP2A promotes cancer growth by coordinating the activities of MTORC1 and MYC.

作者信息

Puustinen Pietri, Jäättelä Marja

机构信息

Cell Death and Metabolism; Danish Cancer Society Research Center (DCRC); Copenhagen, Denmark.

出版信息

Autophagy. 2014 Jul;10(7):1352-4. doi: 10.4161/auto.29076. Epub 2014 May 15.

Abstract

KIAA1524/CIP2A/cancerous inhibitor of protein phosphatase 2A is a cancer-promoting protein that stabilizes the MYC proto-oncogene protein by inhibiting its dephosphorylation. Our recent report demonstrates that KIAA1524/CIP2A supports cancer cell growth also at the level of the mechanistic target of rapamycin complex 1 (MTORC1), a key signaling module that drives cell growth by stimulating protein synthesis and inhibiting autophagy. KIAA1524/CIP2A suppresses MTORC1-associated protein phosphatase 2A (PP2A) activity in an allosteric manner thereby stabilizing the phosphorylation of MTORC1 substrates and keeping the cell in an anabolic mode. In the absence of growth stimulating signals or nutrients, reduced MTORC1 activity triggers SQSTM1/p62-dependent autophagic degradation of KIAA1524/CIP2A enhancing the PP2A-mediated dephosphorylation of MTORC1 substrates and MYC. Thus, KIAA1524/CIP2A emerges as an oncoprotein that can coordinate the growth-promoting activities of MTORC1 and MYC in response to environmental and intrinsic cues.

摘要

KIAA1524/CIP2A/蛋白磷酸酶2A的癌性抑制剂是一种促进癌症的蛋白,它通过抑制原癌基因蛋白MYC的去磷酸化作用来使其稳定。我们最近的报告表明,KIAA1524/CIP2A在雷帕霉素复合物1(MTORC1)的机制靶点水平上也支持癌细胞生长,MTORC1是一个关键的信号模块,通过刺激蛋白质合成和抑制自噬来驱动细胞生长。KIAA1524/CIP2A以变构方式抑制MTORC1相关的蛋白磷酸酶2A(PP2A)活性,从而稳定MTORC1底物的磷酸化并使细胞保持在合成代谢模式。在没有生长刺激信号或营养物质的情况下,MTORC1活性降低会触发SQSTM1/p62依赖性的KIAA1524/CIP2A自噬降解,增强PP2A介导的MTORC1底物和MYC的去磷酸化。因此,KIAA1524/CIP2A作为一种癌蛋白出现,它可以根据环境和内在线索协调MTORC1和MYC的促生长活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8902/4203564/a67d22105b15/auto-10-1352-g1.jpg

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