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微小 RNA-497-5p 的下调增加了肾透明细胞癌中 PD-L1 的表达。

MicroRNA-497-5p down-regulation increases PD-L1 expression in clear cell renal cell carcinoma.

机构信息

a Department of Urology , The Third Affiliated Hospital of Second Military Medical University , Shanghai , China.

b Department of Urology , Changzheng Hospital of Second Military Medical University , Shanghai , China.

出版信息

J Drug Target. 2019 Jan;27(1):67-74. doi: 10.1080/1061186X.2018.1479755. Epub 2018 Sep 11.

Abstract

Recent advances in immunotherapy are raising hope to treat clear cell renal cell carcinoma (ccRCC) with PD-L1 inhibitors, but only a small portion of patients are PD-L1 positive. The heterogeneous expression pattern of PD-L1 in patient population suggests that PD-L1 expression is under the control of diverse regulatory mechanisms. Although recent studies have identified numerous novel PD-L1 regulators, reports on microRNAs which modulate PD-L1 expression are much scarce. In this study, we confirmed that PD-L1 expression was up-regulated in ccRCC compared to paired normal tissues. Using miRDB and miRTarBase, 11 microRNAs were predicted to target PD-L1. After measuring the microRNA panel with TaqMan assays, we found that microRNA-497-5p down-regulation was associated with PD-L1 up-regulation. In TCGA-KIRC dataset, microRNA-497-5p down-regulation was also associated with PD-L1 up-regulation as well as shorter survival. We further validated that PD-L1 was a direct target of microRNA-497-5p in two RCC cell lines. In addition, microRNA-497-5p inhibited cell proliferation, clone formation and migration, while promoted apoptosis in in-vitro assays. Our study reveals a novel regulatory mechanism of PD-L1 expression and the potential of miR-497-5p as therapeutic target and biomarker deserves further investigation.

摘要

免疫疗法的最新进展为治疗 PD-L1 抑制剂的透明细胞肾细胞癌(ccRCC)带来了希望,但只有一小部分患者 PD-L1 呈阳性。PD-L1 在患者人群中的异质性表达模式表明 PD-L1 的表达受多种调控机制的控制。尽管最近的研究已经确定了许多新的 PD-L1 调节剂,但关于调节 PD-L1 表达的 microRNA 的报道却很少。在这项研究中,我们证实与配对的正常组织相比,ccRCC 中 PD-L1 的表达上调。使用 miRDB 和 miRTarBase,预测了 11 个 microRNA 靶向 PD-L1。在使用 TaqMan 测定法测量 microRNA 谱后,我们发现 microRNA-497-5p 的下调与 PD-L1 的上调有关。在 TCGA-KIRC 数据集,microRNA-497-5p 的下调也与 PD-L1 的上调以及较短的生存时间有关。我们进一步验证了 microRNA-497-5p 是两种 RCC 细胞系中 PD-L1 的直接靶标。此外,microRNA-497-5p 在体外实验中抑制细胞增殖、克隆形成和迁移,同时促进细胞凋亡。我们的研究揭示了 PD-L1 表达的新调控机制,microRNA-497-5p 作为治疗靶点和生物标志物的潜力值得进一步研究。

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