论著·基础研究

UBE3C对卵巢癌SKOV3细胞增殖和侵袭能力的影响

  • 徐华丽 ,
  • 刘文雪 ,
  • 沈方倩 ,
  • 席晓薇
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  • 上海交通大学附属第一人民医院妇产科,上海200080
徐华丽(1990—),女,硕士生;电子信箱:xuhualisjtu@126.com。

网络出版日期: 2018-07-03

基金资助

上海市科学技术委员会课题(15411952300)

Effects of UBE3C on proliferation and invasion in ovarian cancer SKOV3 cells

  • XU Hua-li ,
  • LIU Wen-xue ,
  • SHEN Fang-qian ,
  • XI Xiao-wei
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  • Department of Obstetrics and Gynecology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200080

Online published: 2018-07-03

Supported by

Foundation of Science and Technology Commission of Shanghai Municipality, 15411952300

摘要

目的·探讨泛素连接酶E3C(ubiquitin protein ligase E3C,UBE3C)对卵巢癌SKOV3细胞增殖、侵袭能力的影响。方法· Western blotting法检测UBE3C蛋白在不同卵巢癌细胞株和正常卵巢上皮细胞中的表达。选择卵巢癌SKOV3细胞株转染si-UBE3C下调UBE3C表达,转染ex-UBE3C质粒上调UBE3C表达。CCK-8法、平板克隆实验检测细胞增殖能力的变化,细胞划痕、Transwell侵袭实验检测细胞迁移、侵袭能力的变化,并检测增殖、转移相关蛋白β-catenin、c-Myc的表达。结果· UBE3C在卵巢癌细胞株中的表达显著高于正常卵巢上皮细胞。si-UBE3C转染SKOV3细胞沉默UBE3C表达,细胞增殖能力下降,迁移及侵袭能力减弱,β-catenin、c-Myc蛋白表达下调。ex-UBE3C转染后UBE3C过表达,SKOV3细胞增殖、迁移、侵袭能力增强,且β-catenin、c-Myc蛋白表达水平升高。结论· UBE3C可能通过上调β-catenin及c-Myc蛋白表达,增强卵巢癌SKOV3细胞的增殖、侵袭能力。

本文引用格式

徐华丽 , 刘文雪 , 沈方倩 , 席晓薇 . UBE3C对卵巢癌SKOV3细胞增殖和侵袭能力的影响[J]. 上海交通大学学报(医学版), 2018 , 38(6) : 610 . DOI: 10.3969/j.issn.1674-8115.2018.06.005

Abstract

Objective · To explore the effects of ubiquitin protein ligase E3C (UBE3C) on proliferation and invasion in epithelial ovarian cancer SKOV3cells. Methods · Western blotting was used to detect the difference of UBE3C in epithelial ovarian cancer cell lines and normal ovarian cell lines. SKOV3 cells were transfected with si-UBE3C to knockdown UBE3C protein level, while ex-UBE3C plasmid was used to upregulate the of UBE3C. Cell proliferation was measuredCCK-8 assay and colony formation assay. Wound healing assay and Transwell assay were performed to investigate the effect of UBE3C on migration and invasion. Protein levels of β-catenin and c-Myc were also detected in different groups, which were closely related to proliferation and invasion. Results · UBE3C was highly expressed in epithelial ovarian cancer cell lines. UBE3C was successfully silenced with si-UBE3C transfection in SKOV3 cells. Inhibition of UBE3C significantly weakened the abilities of cell proliferation, migration and invasion. A reduction of β-catenin and c-Myc protein levels was also accompaniedUBE3C knockdown. Over of UBE3C with exUBE3Cplasmid promoted the abilities of proliferation, migration and invasion. Enhanced levels of β-catenin and c-Myc were also verified. Conclusion · UBE3C promotes proliferation and invasion of epithelial ovarian cancer SKOV3 cells. This might be to do with upregulation of β-catenin and c-Myc protein levels.
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