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SCC-S2在结肠癌中过度表达并调节细胞增殖。

SCC-S2 is overexpressed in colon cancers and regulates cell proliferation.

作者信息

Miao Zhifeng, Zhao Tingting, Wang Zhenning, Xu Yingying, Song Yongxi, Wu Jianhua, Xu Huimian

机构信息

Department of General Surgery, First Affiliated Hospital of China Medical University, Shenyang, China.

出版信息

Tumour Biol. 2012 Dec;33(6):2099-106. doi: 10.1007/s13277-012-0469-1. Epub 2012 Aug 12.

Abstract

SCC-S2 was recently reported to be overexpressed in various cancers and associated with the malignant behavior of cancer cells. However, the expression of SCC-S2 and its biological roles in colon cancers have not been reported. The aim of this study is to investigate the expression and clinical significance of SCC-S2 in colon cancers and explore its biological function in colon cancer cells. We analyzed the expression pattern of SCC-S2 in 92 colon cancer tissues by immunohistochemistry and found that SCC-S2 was overexpressed in 45 (48.9 %) of 92 colon cancer specimens. There was a significant association between SCC-S2 overexpression and TNM stage (p = 0.0387), lymph node metastasis (p = 0.0219), and proliferation index (p = 0.0279). siRNA knockdown of SCC-S2 expression in CACO2 and HCT116 cells decrease cell proliferation, colony formation, and soft agar colony formation ability. Furthermore, western blot analysis showed that SCC-S2 depletion decreased cyclin D1 and phospho-Rb levels. In conclusion, we demonstrated that SCC-S2 is overexpressed in colon cancers and contributes to malignant cell growth by cyclin D1 and phospho-Rb modulation, which makes SCC-S2 a candidate therapeutic target in colon cancer.

摘要

最近有报道称SCC - S2在多种癌症中过表达,并与癌细胞的恶性行为相关。然而,SCC - S2在结肠癌中的表达及其生物学作用尚未见报道。本研究的目的是探讨SCC - S2在结肠癌中的表达及临床意义,并探索其在结肠癌细胞中的生物学功能。我们通过免疫组织化学分析了92例结肠癌组织中SCC - S2的表达模式,发现92例结肠癌标本中有45例(48.9%)SCC - S2过表达。SCC - S2过表达与TNM分期(p = 0.0387)、淋巴结转移(p = 0.0219)和增殖指数(p = 0.0279)之间存在显著相关性。在CACO2和HCT116细胞中,通过小干扰RNA敲低SCC - S2的表达可降低细胞增殖、集落形成和软琼脂集落形成能力。此外,蛋白质印迹分析表明,SCC - S2表达缺失会降低细胞周期蛋白D1和磷酸化Rb的水平。总之,我们证明了SCC - S2在结肠癌中过表达,并通过调节细胞周期蛋白D1和磷酸化Rb促进恶性细胞生长,这使得SCC - S2成为结肠癌的一个候选治疗靶点。

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