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HBx 通过增加 DDX17 促进 HBV 相关肝细胞癌的发生。

HBx Mediated Increase of DDX17 Contributes to HBV-Related Hepatocellular Carcinoma Tumorigenesis.

机构信息

Key Laboratory of Molecular Biology for Infectious Diseases, Chinese Ministry of Education, Chongqing Medical University, Chongqing, China.

出版信息

Front Immunol. 2022 Jun 16;13:871558. doi: 10.3389/fimmu.2022.871558. eCollection 2022.

Abstract

HBV is strongly associated with HCC development and DEAD-box RNA helicase 17 (DDX17) is a very important member of the DEAD box family that plays key roles in HCC development by promoting cancer metastasis. However, the important role of DDX17 in the pathogenesis of HBV-related HCC remains unclear. In this study, we investigated the role of DDX17 in the replication of HBV and the development of HBV-associated HCC. Based on data from the GEO database and HBV-infected cells, we found that DDX17 was upregulated by the HBV viral protein X (HBx). Mechanistically, increased DDX17 expression promoted HBV replication and transcription by upregulating ZWINT. Further study showed that DDX17 could promote HBx-mediated HCC metastasis. Finally, the promotive effect of DDX17 on HBV and HBV-related HCC was confirmed . In summary, the results revealed the novel role of DDX17 in the replication of HBV and the metastasis of HBV-associated HCC.

摘要

HBV 与 HCC 的发生发展密切相关,DEAD -box RNA 解旋酶 17(DDX17)是 DEAD -box 家族的一个重要成员,它通过促进癌症转移在 HCC 的发生发展中发挥关键作用。然而,DDX17 在 HBV 相关 HCC 发病机制中的重要作用尚不清楚。在本研究中,我们研究了 DDX17 在 HBV 复制和 HBV 相关 HCC 发生发展中的作用。基于 GEO 数据库和 HBV 感染细胞的数据,我们发现 DDX17 被 HBV 病毒蛋白 X(HBx)上调。在机制上,DDX17 表达的增加通过上调 ZWINT 促进了 HBV 的复制和转录。进一步的研究表明,DDX17 可以促进 HBx 介导的 HCC 转移。最后,证实了 DDX17 对 HBV 和 HBV 相关 HCC 的促进作用。综上所述,这些结果揭示了 DDX17 在 HBV 复制和 HBV 相关 HCC 转移中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad99/9243429/f88f6b9f41f2/fimmu-13-871558-g001.jpg

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