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REV7 在小细胞肺癌中的表达增加及其与肿瘤细胞存活和增殖的关系。

Increased expression of REV7 in small cell lung carcinomas and its association with tumor cell survival and proliferation.

机构信息

Department of Pathology, Kitasato University School of Medicine, Kanagawa, Japan.

出版信息

Pathol Int. 2021 Jan;71(1):15-23. doi: 10.1111/pin.13040. Epub 2020 Oct 28.

Abstract

REV7 is involved in multiple biological processes including DNA damage tolerance, cell cycle regulation and gene expression, and is an accessory subunit of the mutation-prone DNA polymerase ζ. It has been reported that REV7 expression is associated with poor prognosis in several human cancers. The aim of this study is to investigate the significance of REV7 in lung carcinogenesis. Immunohistochemical analyses of surgically resected lung cancer specimens revealed that REV7 shows an increased expression in small cell lung carcinomas (SCLCs) when compared with other histological types of lung carcinoma. Association between REV7 expression levels and clinicopathological factors was investigated using SCLC cases with or without surgical resection. Our analyses revealed that high REV7 expression significantly correlated with tumor cell proliferation, assessed by Ki-67 labeling indices, and was negatively associated with distant metastasis and extensive-stage disease. No significant association was detected between REV7 expression and other factors, including prognosis or response to chemoradiotherapy in SCLC. Increase in REV7 expression in SCLC was confirmed using SCLC cell lines. In addition, siRNA-mediated depletion of REV7 activated the apoptotic pathway and suppressed cell growth in SCLC cells. These results suggest that REV7 plays an important role in tumor cell survival and proliferation in SCLC.

摘要

REV7 参与多种生物学过程,包括 DNA 损伤耐受、细胞周期调控和基因表达,是易错 DNA 聚合酶 ζ 的辅助亚基。有报道称,REV7 的表达与几种人类癌症的不良预后相关。本研究旨在探讨 REV7 在肺癌发生中的意义。对手术切除的肺癌标本进行免疫组织化学分析表明,与其他肺癌组织学类型相比,REV7 在小细胞肺癌(SCLC)中表达增加。使用有或无手术切除的 SCLC 病例研究了 REV7 表达水平与临床病理因素之间的关系。我们的分析表明,高 REV7 表达与 Ki-67 标记指数评估的肿瘤细胞增殖显著相关,并且与远处转移和广泛期疾病呈负相关。在 SCLC 中,未检测到 REV7 表达与其他因素(包括预后或对放化疗的反应)之间存在显著关联。使用 SCLC 细胞系证实了 SCLC 中 REV7 表达的增加。此外,siRNA 介导的 REV7 耗竭激活了凋亡途径并抑制了 SCLC 细胞的生长。这些结果表明,REV7 在 SCLC 中的肿瘤细胞存活和增殖中发挥重要作用。

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