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干扰素调节因子1通过靶向自噬相关蛋白13抑制自噬介导的结直肠癌增殖。

IRF1 Inhibits Autophagy-Mediated Proliferation of Colorectal Cancer via Targeting ATG13.

作者信息

Yuan Li, Zhang Xiao, Cheng Kai, Li Liping, Guo Zhongming, Zeng Liang

机构信息

Department of Pathology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Department of Gastrointestinal Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

出版信息

Cancer Invest. 2022 Jan;40(1):35-45. doi: 10.1080/07357907.2021.1961265. Epub 2021 Aug 17.

Abstract

IRF1 is a nuclear transcription factor that mediates interferon effects and appears to have anti-tumor activity. To determine the roles of IRF1 in colorectal cancer (CRC), we investigated the effects of IRF1 in CRC cells. We found that IRF1 inhibit cell proliferation and tumor growth. Under starvation conditions, IRF1 enhanced apoptosis and reduced autophagic flux. ATG13, an important factor of autophagy complex, was confirmed as a target of IRF1. These findings indicated that IRF1 function as a tumor suppressor in CRC and inhibit autophagy through ATG13, targeting this pathway may provide new insights into the molecular mechanisms of CRC progression.

摘要

IRF1是一种核转录因子,可介导干扰素效应,似乎具有抗肿瘤活性。为了确定IRF1在结直肠癌(CRC)中的作用,我们研究了IRF1在CRC细胞中的作用。我们发现IRF1抑制细胞增殖和肿瘤生长。在饥饿条件下,IRF1增强细胞凋亡并减少自噬通量。自噬复合体的一个重要因子ATG13被确认为IRF1的一个靶点。这些发现表明,IRF1在CRC中作为一种肿瘤抑制因子发挥作用,并通过ATG13抑制自噬,针对这一途径可能为CRC进展的分子机制提供新的见解。

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