[Analysis different transcriptional factors in different phenotype endometrial cancer cells]

Zhonghua Fu Chan Ke Za Zhi. 2009 Mar;44(3):209-13.
[Article in Chinese]

Abstract

Objective: To analysis the activity of transcriptional factors in endometrial cancer cell lines with different estrogen receptor subtypes.

Methods: The mRNA levels of estrogen receptor (ER) was detected by quantitative RT-PCR, and the activity of transcriptional factors was also analysed by 345-channel protein/DNA array in RL-952 (the expression status of ERalpha and ERbeta both positive), HEC-1A [ERalpha (+/-), while ERbeta negative] and HEC-1B (ERalpha and ERbeta both negative). The transcription factors of NFkappaBp65 and p38MAPK with different activity were tested by enzyme-linked immunosorbent assay (ELISA) to confirm the results of protein/DNA array.

Results: The mRNA levels of ERalpha in RL-952, HEC-1A and HEC-1B were (6780+/-282), (684+/-84) and (168+/-38) copy/ng, respectively. Among 345 candidate transcriptional factors, there were 28 factors associated with ER status. Compared with RL-952 cells, 13 transcriptional activity factors were concomitantly up-regulation, while 15 concomitantly down-regulation in HEC-1A and HEC-1B cells. Transcriptional activities of TTF (1)-1, NRF-1, TCE were significantly correlated with the high-expression status of ERalpha mRNA (r=0.523, P=0.037), while RFX123 and Ikaros were significantly correlated with the low-expression status of ERalpha mRNA (r=-0.312, P=0.041).

Conclusion: Transcriptional factors of TTF (1)-1, NRF-1, TCE may be associated with ER-mediated signal pathway, while RFX123 and Ikaros may be associated with non ER-mediated signal pathway in endometrial cancer.

Publication types

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

MeSH terms

  • Cell Line, Tumor
  • Endometrial Neoplasms / metabolism*
  • Endometrial Neoplasms / pathology
  • Enzyme-Linked Immunosorbent Assay
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / physiology*
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / physiology*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Transcription Factor RelA / metabolism*
  • Transcription Factors / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • RNA, Messenger
  • Transcription Factor RelA
  • Transcription Factors
  • p38 Mitogen-Activated Protein Kinases