4.4 Article

Loss of ARID1A/BAF250a expression is linked to tumor progression and adverse prognosis in cervical cancer

期刊

HUMAN PATHOLOGY
卷 44, 期 7, 页码 1365-1374

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.humpath.2012.11.007

关键词

ARID1A/BAF250a; Cervical cancer; Immunohistochemistry; Prognostic marker; Tissue microarray

资金

  1. Basic Science Research Program through the National Research Foundation of Korea
  2. Ministry of Education, Science and Technology [2011-0005230, 2011-0010286, 2011-0007146]
  3. Yonsei University College of Medicine [3-2010-0072, 6-2011-0073]
  4. National Research Foundation of Korea [2011-0010286, 2011-0007146] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The tumor suppressor gene ARID1A encodes BAF250a, a component of human SWI/SNF chromatin-remodeling complexes. Loss of BAF250a expression has recently been reported in several tumor types. To investigate the potential correlation between BAF250a and various clinicopathologic parameters, we assessed the expression of BAF250a in archival tumor tissue specimens from 147 patients with cervical cancer and 191 with cervical intraepithelial neoplasia as well as 376 matched nonadjacent normal tissues by immunohistochemical staining. Messenger RNA expression level for BAF250a was decreased in cervical cancer cell lines (P = .013) and tissues (P = .010), when compared with normal cervical epithelial tissue using SYBR Green real-time polymerase chain reaction. BAF250a was also detected in nuclear fractions of HeLa cells and in nuclei of cervical cancer tissue samples by Western blotting and immunohistochemistry, respectively. BAF250a expression gradually decreased in transitioning from normal to cervical carcinoma (P < .001), and this loss of expression was significantly associated with tumor stage (P = .005), tumor grade (P = .029), tumor size (P = .003), and lymph node metastasis (P = .020). In multivariate analysis, overall survival in cervical cancer was significantly reduced in cases with BAF250a loss (hazard ratio, 2.78 [1.01-7.63]; P = .047). Our findings suggest a potential role for BAF250a in providing valuable prognostic information to clinicians for risk assessment in cervical cancer. (C) 2013 Elsevier Inc. All rights reserved.

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