ELP3稳定c-myc以促进肿瘤发生。

IF 5.3 2区 生物学 Q2 CELL BIOLOGY Journal of Molecular Cell Biology Pub Date : 2024-04-04 DOI:10.1093/jmcb/mjad059
Wentao Zhao, Cong Ouyang, Chen Huang, Jiaojiao Zhang, Qiao Xiao, Fengqiong Zhang, Huihui Wang, Furong Lin, Jinyang Wang, Zhanxiang Wang, Bin Jiang, Qinxi Li
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引用次数: 0

摘要

ELP3是Elongator复合物的催化亚基,是一种乙酰转移酶,与肿瘤进展有关。然而,ELP3致癌功能的细节在很大程度上仍不清楚。在这里,我们发现ELP3稳定c-Myc,以非依赖于乙酰转移酶的方式促进肿瘤发生。在机械上,ELP3与E3连接酶FBXW7β竞争c-Myc结合,导致FBXW8β介导的c-Myc的泛素化和蛋白酶体降解受到抑制。ELP3敲低减少了糖酵解和谷氨酰胺解,并通过下调c-Myc显著延缓细胞增殖和异种移植物生长,并且通过重建c-Myc表达来挽救这种影响。此外,ELP3和c-Myc在结直肠癌癌症和肝细胞癌中过表达,且呈正相关。总之,我们阐明了ELP3通过稳定c-Myc促进肿瘤发生的新功能,表明抑制ELP3是治疗c-Myc驱动的癌症的潜在策略。
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ELP3 stabilizes c-Myc to promote tumorigenesis.

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.

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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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