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miR-375 通过阻断 JAK2/STAT1 信号通路抑制头颈部鳞状细胞癌细胞中 IFN-γ 诱导的程序性死亡受体 1 配体 1 表面表达。

miR-375 inhibits IFN-γ-induced programmed death 1 ligand 1 surface expression in head and neck squamous cell carcinoma cells by blocking JAK2/STAT1 signaling.

机构信息

Department of Ear, Nose and Throat, The Ninth Affliated Hospital of Shanghai Jiao Tong University, Shanghai 200011, P.R. China.

出版信息

Oncol Rep. 2018 Mar;39(3):1461-1468. doi: 10.3892/or.2018.6177. Epub 2018 Jan 2.

Abstract

Upregulation of programmed death 1 ligand 1 (PD-L1) in cancer cells and its ligation to PD-1 on T cells facilitates cancer cell escape from immune surveillance. Therapies with PD-1 or PD-L1 antibodies have resulted in marked clinical responses in various cancer types. Hence, modulators that inhibit PD-L1 expression in cancer cells may serve as a novel strategy by which to enhance host immune responses. In the present study, we investigated the effects of miR-375 on PD-L1 expression in head and neck squamous cell carcinoma (HNSCC) cells by qRT-PCR and western blot analyses. We confirmed that miR-375 inhibited IFN-γ-induced PD-L1 surface expression in HNSCC cells, and we observed that Janus kinase 2 (JAK2) is a bona fide target of miR-375 and further activated signal transducer and activator of transcription 1 (STAT1). Additionally, miR-375-mediated inhibition of PD-L1 expression was dependent on the JAK2/STAT1 pathway. Therefore, by attenuating PD-1/PD-L1 signaling, miR-375 may also serve as a modulator to increase the cell immune responses to HNSCC.

摘要

程序性死亡受体 1 配体 1(PD-L1)在癌细胞中的上调及其与 T 细胞上的 PD-1 的结合,促进了癌细胞逃避免疫监视。PD-1 或 PD-L1 抗体的治疗在各种癌症类型中产生了显著的临床反应。因此,抑制癌细胞中 PD-L1 表达的调节剂可能成为增强宿主免疫反应的一种新策略。在本研究中,我们通过 qRT-PCR 和 Western blot 分析研究了 miR-375 对头颈鳞状细胞癌(HNSCC)细胞中 PD-L1 表达的影响。我们证实 miR-375 抑制 IFN-γ诱导的 HNSCC 细胞 PD-L1 表面表达,并且观察到 Janus 激酶 2(JAK2)是 miR-375 的真正靶标,并进一步激活信号转导和转录激活因子 1(STAT1)。此外,miR-375 介导的 PD-L1 表达抑制依赖于 JAK2/STAT1 通路。因此,通过减弱 PD-1/PD-L1 信号,miR-375 也可能作为一种调节剂,增加细胞对 HNSCC 的免疫反应。

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