[Expressions of stromal cell-derived factor-1 and CXCR4 in endometrial carcinoma tissues and cell lines]

Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Oct 18;38(5):458-62.
[Article in Chinese]

Abstract

Objective: To investigate the expressions of SDF-1 and CXCR4 in human endometrial carcinoma tissues.

Methods: SDF-1 and CXCR4 protein expression levels were detected by immunohistochemical staining in 26 cases of atypic hyperplasia endometrium,simple hyperplasia endometrium and normal endometrium and 44 cases of endometrial carcinoma tissues.

Results: Both SDF-1 mRNA and CXCR4 mRNA were expressed in Ishikawa, while no expression of SDF-1 mRNA was detected in HEC-1A. The rates of CXCR4 and SDF-1 protein expressions were 100% in glandular cells of human normal endometrial tissues, while 90.9% and 93.2% in glandular cells of endometrial carcinoma tissues. These immunoreactivities of SDF-1 and CXCR4 were significantly low in endometrial carcinoma tissues as compared with those in normal endometrium; and the intensities of immunohistochemical staining significantly decreasesd in immunoreactivity of SDF-1 and CXCR4 in low grade as compared with that in hight grade.

Conclusion: SDF-1 and CXCR4 were expressed differently in endometrial cell lines, human normal endometrial tissues,and endometrial carcinoma tissues. As compared with normal endometrium ,these were significantly low levels expression of SDF-1 and CXCR4 in endometrial carcinoma tissues.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Cell Line, Tumor
  • Chemokine CXCL12 / biosynthesis
  • Chemokine CXCL12 / genetics*
  • Endometrial Neoplasms / genetics
  • Endometrial Neoplasms / metabolism
  • Endometrial Neoplasms / pathology*
  • Endometrium / cytology
  • Endometrium / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Immunohistochemistry
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, CXCR4 / biosynthesis
  • Receptors, CXCR4 / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • CXCL12 protein, human
  • Chemokine CXCL12
  • RNA, Messenger
  • Receptors, CXCR4