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PRDX2通过与PKM2/STAT3轴形成反馈环促进胃癌进展。

PRDX2 promotes gastric cancer progression by forming a feedback loop with PKM2/STAT3 axis.

作者信息

Zhou Yue, Wang Maoye, Qian Yu, Yu Dan, Zhang Jiahui, Fu Min, Zhang Xiaoxin, Qin Rong, Ji Runbi, Zhang Xu, Gu Jianmei

机构信息

Department of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang 212013, China; Kunshan Biomedical Big Data Innovation Application Laboratory, Kunshan Hospital Affiliated to Jiangsu University /Kunshan First People's Hospital, Kunshan 215300, China.

Department of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang 212013, China.

出版信息

Cell Signal. 2025 Mar;127:111586. doi: 10.1016/j.cellsig.2024.111586. Epub 2025 Jan 4.

Abstract

Peroxiredoxin 2 (PRDX2) is an antioxidant enzyme that has been reported to be overexpressed in various cancers. However, the role of PRDX2 in gastric cancer progression and its underlying mechanism remains unclear. Herein, we revealed the function of PRDX2 in gastric cancer progression and explored its molecule mechanism. We identified that PRDX2 was upregulated and associated with poor prognosis in gastric cancer. The knockdown of PRDX2 inhibited the proliferation, migration and invasion of gastric cancer cells in vitro and suppressed tumor growth in vivo. Mechanistically, PRDX2 interacted with PKM2 (pyruvate kinase isozyme type M2) and protected PKM2 from ubiquitination and degradation, which enhanced glycolysis in gastric cancer cells. The interaction between PRDX2 and PKM2 also enhanced the binding affinity between PKM2 and importin α5, which induced PKM2 nuclear translocation and activated STAT3 signaling pathway. In addition, STAT3 (signal transducer and activator of transcription 3) was identified to bind to PRDX2 gene promoter and upregulate PRDX2 expression, which forms a positive regulatory feedback loop in gastric cancer cells. The present study unravels the biological role of PRDX2 in cancer progression and illustrates the underlying molecular mechanism, which may provide a potential therapeutic target for gastric cancer.

摘要

过氧化物酶2(PRDX2)是一种抗氧化酶,据报道在多种癌症中过表达。然而,PRDX2在胃癌进展中的作用及其潜在机制仍不清楚。在此,我们揭示了PRDX2在胃癌进展中的功能,并探讨了其分子机制。我们发现PRDX2在胃癌中上调且与预后不良相关。敲低PRDX2可在体外抑制胃癌细胞的增殖、迁移和侵袭,并在体内抑制肿瘤生长。机制上,PRDX2与丙酮酸激酶M2型同工酶(PKM2)相互作用,保护PKM2不被泛素化和降解,从而增强胃癌细胞的糖酵解。PRDX2与PKM2之间的相互作用还增强了PKM2与输入蛋白α5之间的结合亲和力,诱导PKM2核转位并激活信号转导子及转录激活子3(STAT3)信号通路。此外,还发现STAT3与PRDX2基因启动子结合并上调PRDX2表达,在胃癌细胞中形成正调控反馈环。本研究揭示了PRDX2在癌症进展中的生物学作用,并阐明了潜在的分子机制,这可能为胃癌提供一个潜在的治疗靶点。

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