Liu Youqing, Han Xiaobing, Gao Baoan
Department of Obstetrics and Gynecology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, Anhui 230001, P.R. China.
Department of Obstetrics and Gynecology, The First Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Exp Ther Med. 2015 Apr;9(4):1460-1464. doi: 10.3892/etm.2015.2257. Epub 2015 Feb 3.
As a member of the S100 protein family, S100A11 expression is often upregulated in human cancer tissues. Numerous studies have demonstrated that S100A11 plays an important role in the progression of cancer. However, the function of S100A11 in ovarian cancer remains elusive. In the present study, the expression levels of S100A11 were found to be significantly increased in ovarian cancer cells. Subsequently, the expression of S100A11 in ovarian cancer HO8910 cells was knocked down using short hairpin (sh)RNA in order to investigate the biological effects of S100A11 on the progression of the disease. The results demonstrated that knockdown of S100A11 by shRNA inhibited the proliferation, anchorage-independent growth, invasion and migration of HO8910 cells. In addition, knockdown of S100A11 increased the expression of E-cadherin and decreased the expression of Snail in HO8910 cells. Collectively, these results indicated that S100A11 was able to promote the growth, invasion and migration of ovarian cancer cells. Therefore, S100A11 may serve as a potential molecular target for the diagnosis and treatment of ovarian cancer.
作为S100蛋白家族的一员,S100A11在人类癌组织中的表达常常上调。众多研究已证明S100A11在癌症进展中发挥重要作用。然而,S100A11在卵巢癌中的功能仍不清楚。在本研究中,发现S100A11在卵巢癌细胞中的表达水平显著升高。随后,为了研究S100A11对该疾病进展的生物学效应,使用短发夹(sh)RNA敲低了卵巢癌HO8910细胞中S100A11的表达。结果表明,shRNA敲低S100A11可抑制HO8910细胞的增殖、非锚定依赖性生长、侵袭和迁移。此外,敲低S100A11可增加HO8910细胞中E-钙黏蛋白的表达并降低Snail的表达。总体而言,这些结果表明S100A11能够促进卵巢癌细胞的生长、侵袭和迁移。因此,S100A11可能作为卵巢癌诊断和治疗的潜在分子靶点。