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Spy1参与上皮性卵巢癌的增殖和凋亡。

Spy1 participates in the proliferation and apoptosis of epithelial ovarian cancer.

作者信息

Lu Shumin, Liu Rong, Su Min, Wei Yingze, Yang Shuyun, He Song, Wang Xia, Qiang Fulin, Chen Chen, Zhao Shuyang, Zhang Weiwei, Xu Pan, Mao Guoxin

机构信息

Department of Oncology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.

Department of Pathology, Nantong University Cancer Hospital, Nantong, 226001, Jiangsu Province, People's Republic of China.

出版信息

J Mol Histol. 2016 Feb;47(1):47-57. doi: 10.1007/s10735-015-9646-z. Epub 2015 Dec 7.

Abstract

This study focused on determining the role of Spy1 in human epithelial ovarian cancer (EOC). Speedy is a novel cell cycle protein capable of promoting cell proliferation. In this study, western blot and immunohistochemistrical analyses were performed to detect the expression of Spy1 in ovarian cancer. Spy1 protein levels increased with ovarian cancer grade, and Kaplan-Meier curve showed that overexpression of Spy1 was significantly correlated with reduced patient survival. In vitro, Spy1 depletion in ovarian cell lines led to reduced proliferation according to CCK8 and plate colony assays. The expression of Spy1 was positively related to pThr187-p27. Flow cytometry revealed that the reduced expression of Spy1 induced the apoptosis of the EOC cells. In summary, our findings suggested that Spy1 may be a novel independent prognostic predictor of survival for ovarian patients.

摘要

本研究聚焦于确定Spy1在人上皮性卵巢癌(EOC)中的作用。Speedy是一种能够促进细胞增殖的新型细胞周期蛋白。在本研究中,进行了蛋白质印迹法和免疫组织化学分析以检测Spy1在卵巢癌中的表达。Spy1蛋白水平随卵巢癌分级增加而升高,Kaplan-Meier曲线显示Spy1过表达与患者生存率降低显著相关。在体外,根据CCK8和平板集落试验,卵巢细胞系中Spy1缺失导致增殖减少。Spy1的表达与pThr187-p27呈正相关。流式细胞术显示Spy1表达降低诱导了EOC细胞凋亡。总之,我们的研究结果表明Spy1可能是卵巢癌患者生存的一种新型独立预后预测指标。

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