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促生存的 Oct4/Stat1/Mcl-1 轴与肺腺癌患者的不良预后相关。

The Pro-Survival Oct4/Stat1/Mcl-1 Axis Is Associated with Poor Prognosis in Lung Adenocarcinoma Patients.

机构信息

Department of Otolaryngology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 70403, Taiwan.

Department of Biochemistry and Molecular Biology, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

Cells. 2021 Oct 3;10(10):2642. doi: 10.3390/cells10102642.

Abstract

The embryonic stem cell marker Oct4 is expressed in several human cancers and is positively correlated with a poor outcome in cancer patients. However, its physiological role in cancer progression remains poorly understood. Tumor cells block apoptosis to escape cell death so that they can proliferate indefinitely, leading to ineffective therapy for cancer patients. In this study, we investigated whether Oct4 regulates the apoptosis pathway and contributes to poor prognosis in patients with lung adenocarcinoma. Our results revealed that Oct4 expression is correlated with Stat1 expression in lung adenocarcinoma patients and Oct4 is directly bound to the promoter to transactivate Stat1 in lung adenocarcinoma cells. Expression of the Stat1 downstream gene Mcl-1 increased in Oct4-overexpressing cancer cells, while Stat1 knockdown in Oct4-overexpressing cancer cells sensitized them to cisplatin-induced apoptosis. Furthermore, Oct4 promoted Stat1 expression and tumor growth, whereas silencing of Stat1 reduced Oct4-induced tumor growth in human lung tumor xenograft models. Taken together, we demonstrate that Oct4 is a pro-survival factor by inducing Stat1 expression and that the Oct4/Stat1/Mcl-1 axis may be a potential therapeutic target for lung adenocarcinoma.

摘要

胚胎干细胞标志物 Oct4 在多种人类癌症中表达,并与癌症患者的不良预后呈正相关。然而,其在癌症进展中的生理作用仍知之甚少。肿瘤细胞阻止细胞凋亡以逃避细胞死亡,从而使其能够无限增殖,导致癌症患者的治疗无效。在这项研究中,我们研究了 Oct4 是否调节细胞凋亡途径并导致肺腺癌患者预后不良。我们的结果表明,Oct4 在肺腺癌患者中与 Stat1 的表达相关,并且 Oct4 直接结合到肺腺癌细胞中的启动子上以反式激活 Stat1。在过表达 Oct4 的癌细胞中,Stat1 下游基因 Mcl-1 的表达增加,而在过表达 Oct4 的癌细胞中敲低 Stat1 使它们对顺铂诱导的细胞凋亡敏感。此外,Oct4 促进 Stat1 表达和肿瘤生长,而沉默 Stat1 则减少了 Oct4 诱导的人肺肿瘤异种移植模型中的肿瘤生长。综上所述,我们证明了 Oct4 通过诱导 Stat1 表达成为一种生存促进因子,并且 Oct4/Stat1/Mcl-1 轴可能是肺腺癌的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f58/8534205/7432ce3c6ee7/cells-10-02642-g001.jpg

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