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MCM8 在结直肠癌发生发展中的功能和作用机制。

Function and mechanism of MCM8 in the development and progression of colorectal cancer.

机构信息

Key Laboratory of Cancer Prevention and Intervention, The Second Affiliated Hospital, Ministry of Education, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, 270 Dong'an Road, Shanghai, 200032, PR China.

出版信息

J Transl Med. 2023 Sep 14;21(1):623. doi: 10.1186/s12967-023-04084-9.

Abstract

Colorectal cancer (CRC) has become a global health problem which has almost highest morbidity and mortality in all types of cancers. This study aimed to uncover the biological functions and underlying mechanism of MCM8 in the development and progression of CRC. The expression level of MCM8 was found to be upregulated in CRC tissues and significantly associated with tumor grade and patients' survival. Knocking down MCM8 expression in CRC cells could restrain cell growth and cell motility while promoting cell apoptosis in vitro, as well as inhibit tumor growth in xenograft mice model. Based on the RNA screening performing on CRC cells with or without MCM8 knockdown and the following IPA analysis, CHSY1 was identified as a potential target of MCM8 in CRC, whose expression was also found to be higher in tumor tissues than in normal tissues. Moreover, it was demonstrated that MCM8 may regulate the expression of CHSY1 through affecting its NEDD4-mediated ubiquitination, both of which synergistically execute tumor promotion effects on CRC. In conclusion, the outcomes of our study showed the first evidence that MCM8 act as a tumor promotor in CRC, and may be a promising therapeutic target of CRC treatment.

摘要

结直肠癌(CRC)已成为全球健康问题,在所有类型的癌症中,CRC 的发病率和死亡率几乎最高。本研究旨在揭示 MCM8 在 CRC 发生和发展中的生物学功能和潜在机制。研究发现,MCM8 在 CRC 组织中表达上调,与肿瘤分级和患者生存显著相关。在体外,敲低 CRC 细胞中的 MCM8 表达可抑制细胞生长和迁移,促进细胞凋亡,在异种移植小鼠模型中抑制肿瘤生长。基于对有无 MCM8 敲低的 CRC 细胞进行的 RNA 筛选,以及随后的 IPA 分析,确定 CHSY1 是 MCM8 在 CRC 中的一个潜在靶点,其在肿瘤组织中的表达也高于正常组织。此外,研究表明 MCM8 可能通过影响其 NEDD4 介导的泛素化来调节 CHSY1 的表达,两者协同作用对 CRC 发挥促肿瘤作用。总之,本研究结果首次表明 MCM8 在 CRC 中作为肿瘤促进因子发挥作用,可能成为 CRC 治疗的有前途的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1041/10503009/568e0ef8ceff/12967_2023_4084_Fig1_HTML.jpg

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