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ELP3通过稳定c-Myc来促进肿瘤发生。

ELP3 stabilizes c-Myc to promote tumorigenesis.

作者信息

Zhao Wentao, Ouyang Cong, Huang Chen, Zhang Jiaojiao, Xiao Qiao, Zhang Fengqiong, Wang Huihui, Lin Furong, Wang Jinyang, Wang Zhanxiang, Jiang Bin, Li Qinxi

机构信息

State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen 361102, China.

Department of Neurosurgery and Department of Neuroscience, Fujian Key Laboratory of Brain Tumors Diagnosis and Precision Treatment, Xiamen Key Laboratory of Brain Center, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen 361003, China.

出版信息

J Mol Cell Biol. 2024 Apr 4;15(9). doi: 10.1093/jmcb/mjad059.

Abstract

ELP3, the catalytic subunit of the Elongator complex, is an acetyltransferase and associated with tumor progression. However, the detail of ELP3 oncogenic function remains largely unclear. Here, we found that ELP3 stabilizes c-Myc to promote tumorigenesis in an acetyltransferase-independent manner. Mechanistically, ELP3 competes with the E3-ligase FBXW7β for c-Myc binding, resulting in the inhibition of FBXW7β-mediated ubiquitination and proteasomal degradation of c-Myc. ELP3 knockdown diminishes glycolysis and glutaminolysis and dramatically retards cell proliferation and xenograft growth by downregulating c-Myc, and such effects are rescued by the reconstitution of c-Myc expression. Moreover, ELP3 and c-Myc were found overexpressed with a positive correlation in colorectal cancer and hepatocellular carcinoma. Taken together, we elucidate a new function of ELP3 in promoting tumorigenesis by stabilizing c-Myc, suggesting that inhibition of ELP3 is a potential strategy for treating c-Myc-driven carcinomas.

摘要

ELP3是延伸因子复合物的催化亚基,是一种乙酰转移酶,与肿瘤进展相关。然而,ELP3致癌功能的细节在很大程度上仍不清楚。在此,我们发现ELP3以不依赖乙酰转移酶的方式稳定c-Myc以促进肿瘤发生。机制上,ELP3与E3连接酶FBXW7β竞争结合c-Myc,导致FBXW7β介导的c-Myc泛素化和蛋白酶体降解受到抑制。ELP3基因敲低通过下调c-Myc减少糖酵解和谷氨酰胺分解,并显著抑制细胞增殖和异种移植瘤生长,而c-Myc表达的恢复可挽救这些效应。此外,在结直肠癌和肝细胞癌中发现ELP3和c-Myc呈正相关且过表达。综上所述,我们阐明了ELP3通过稳定c-Myc促进肿瘤发生的新功能,提示抑制ELP3是治疗c-Myc驱动的癌症的潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83c8/11054291/45376a08baca/mjad059fig1.jpg

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