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WD40 重复包含蛋白 62 过表达可作为人类胃癌预后不良的一个新指标。

WD40 repeat-containing 62 overexpression as a novel indicator of poor prognosis for human gastric cancer.

机构信息

Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Eur J Cancer. 2013 Nov;49(17):3752-62. doi: 10.1016/j.ejca.2013.07.015. Epub 2013 Aug 3.

Abstract

AIM

WD40 repeat-containing 62 (WDR62) is a centrosome-associated gene involved in cell cycling and proliferation. However, the role of WDR62 in human malignancies remains unknown. The present study aimed to identify the role, if any, of WDR62 in the pathogenesis of human gastric cancer (GC).

METHODS

WDR62 expression in 372 cases of human GC and eight GC cell lines was determined using quantitative reverse transcription-polymerase chain reaction (qRT-PCR), immunohistochemistry and Western blotting. Correlations between WDR62 expression and clinicopathological characteristics, as well as GC prognosis were determined. WDR62 regulation of GC cell proliferation, invasion, migration and cell cycle distribution were studied both in vitro and in vivo.

RESULTS

WDR62 expression was significantly increased in GC tissues and cell lines and was associated with poor differentiation and prognosis of GC. WDR62 expression was elevated in GC multidrug resistant cells. Suppressing WDR62 significantly decreased cell proliferation and induced G2/M phase arrest of GC cells. Consistently, WDR62 knockdown inhibited gastric carcinogenesis in nude mice. Regulation of Akt/p38-mitogen-activated protein kinase (MAPK)/multidrug resistance gene 1 (MDR1) expression and activation by WDR62 contributed to the chemoresistance of GC cells. WDR62 overexpresses in GC and the suppression of WDR62 inhibits GC cell growth by inducing G2/M cell cycle arrest.

CONCLUSION

WDR62 may be a novel prognostic marker and a potential chemotherapy target for GC.

摘要

目的

WD40 重复包含蛋白 62(WDR62)是一种与中心体相关的基因,参与细胞周期和增殖。然而,WDR62 在人类恶性肿瘤中的作用尚不清楚。本研究旨在确定 WDR62 在人类胃癌(GC)发病机制中的作用。

方法

采用定量逆转录-聚合酶链反应(qRT-PCR)、免疫组织化学和 Western blot 检测 372 例人 GC 组织和 8 种 GC 细胞系中 WDR62 的表达。分析 WDR62 表达与临床病理特征及 GC 预后的相关性。在体外和体内研究 WDR62 对 GC 细胞增殖、侵袭、迁移和细胞周期分布的调控作用。

结果

WDR62 在 GC 组织和细胞系中的表达明显增加,与 GC 的低分化和预后不良相关。WDR62 在 GC 多药耐药细胞中表达上调。抑制 WDR62 可显著降低 GC 细胞的增殖,并诱导其 G2/M 期阻滞。同样,WDR62 敲低可抑制裸鼠胃发生肿瘤。WDR62 通过调节 Akt/p38-丝裂原活化蛋白激酶(MAPK)/多药耐药基因 1(MDR1)的表达和激活来促进 GC 细胞的耐药性。WDR62 在 GC 中高表达,抑制 WDR62 可通过诱导 G2/M 细胞周期阻滞抑制 GC 细胞生长。

结论

WDR62 可能是 GC 的一种新的预后标志物和潜在的化疗靶点。

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