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[Overexpression of estrogen receptor-related receptor alpha can stimulate estrogen receptor negative endometrial cancer cell proliferation].

AbstractOBJECTIVE:
To investigate the role of human estrogen receptor-related receptor (ERR) alpha, a submember of orphan receptors, in the tumorigenesis of endometrial cancer.
METHODS:
Plasmid of pSG-ERRalpha was transfected into endometrial cancer cell lines HEC-1A, HEC-1B, and Ishikawa. Real-time quantitative RT-PCR and western blot were used to analyze the mRNA and protein expression of ERRalpha in endometrial cancer cell. Flow cytometry was used to analyze the cellular growth.
RESULTS:
Expressions of the ERRalpha were significantly increased in the endometrial cancer cells transfected with pSG-ERRalpha plasmid; expression of the ERRalpha mRNA in HEC-1A cell was 9644.4 copies/ng, HEC-1B: 9835.3 copies/ng, and Ishikawa: 8008.6 copies/ng (P < 0.01); expression of the ERRalpha protein in HEC-1A cell was 1.128, HEC-1B: 1.104, and Ishikawa: 1.008 (P < 0.05). Flow cytometry showed over-expression of ERRalpha was accompanied by increased HEC-1A and HEC-1B cells in S and G(2)/M phase (P < 0.01), while this could not be observed in the estrogen receptor (ER) positive endometrial cancer cell line Ishikawa. Furthermore, cellular growth analysis showed that over-expression of ERRalpha induced cell growth increase of the ER negative endometrial cancer cells HEC-1A and HEC-1B (P < 0.05).
CONCLUSION:
Over-expression of ERRalpha could stimulate ER negative endometrial cancer cell proliferation independent of estrogen-ER pathway.
AuthorsPeng-Ming Sun, Li-Hui Wei, Min Gao, Jian-Liu Wang, Li-Jun Zhao, Da-Peng Wang, Jun-Xiao Zhang
JournalZhonghua fu chan ke za zhi (Zhonghua Fu Chan Ke Za Zhi) Vol. 42 Issue 6 Pg. 408-11 (Jun 2007) ISSN: 0529-567X [Print] China
PMID17697604 (Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • ERRalpha estrogen-related receptor
  • RNA, Messenger
  • Receptors, Estrogen
Topics
  • Blotting, Western
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation
  • Endometrial Neoplasms (genetics, metabolism, pathology)
  • Female
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Plasmids
  • RNA, Messenger (biosynthesis, genetics)
  • Receptors, Estrogen (biosynthesis, genetics, physiology)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transfection

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