Tumorigenesis of K-ras mutation in human endometrial carcinoma via upregulation of estrogen receptor

Gynecol Oncol. 2006 May;101(2):274-9. doi: 10.1016/j.ygyno.2005.10.016. Epub 2005 Nov 21.

Abstract

Objective: To investigate the tumorigenesis of mutant [12Asp]-K-ras in endometrial carcinoma and its relationship with ER.

Methods: We constructed pcDI-[12Asp]K-ras4B by inserting full-length [12Asp]K-ras4B from human endometrial carcinoma Hec-1A cells, into pcDI vector. Cell proliferation of NIH3T3 after transfection with pcDI-[12Asp]K-ras4B was measured by MTT assay. The cell transformation was determined by colony formation and tumor nodule development. [12Asp]-K-ras4B-NIH3T3 cells were transfected with constitutively active pCMV-RafCAAX and dominant-negative pCMV-RafS621A. Cell growth was measured by MTT assay and [3H]thymidine incorporation. After transfected with pcDI-[12Asp]K-ras4B or pCMV-RafS621A, the cells were harvested for Western blot and reporter assay to determine the expression and transcriptional activity of ERalpha and ERbeta, respectively.

Results: [12Asp]-K-ras4B enhanced NIH3T3 cells proliferation after 48 h post-transfection (P < 0.05). More colonies were grown 10 days after incubating pcDI-[12Asp]-K-ras4B-NIH3T3 cells (13.48%) than pcDI-NIH3T3 (4.26%) or untreated NIH3T3 (2.33%). The pcDI-[12Asp]-K-ras4B-NIH3T3 cells injected to the nude mice Balb/C developed tumor nodules with poor-differentiated cells after 12 days. An increase of ERalpha and ERbeta was observed in pcDI-[12Asp]-K-ras4B-NIH3T3 cells. RafS621A downregulated ERalpha and ERbeta expression. Estrogen induced the ER transcriptional activity by 5-fold in pcDI-NIH3T3 cells, 13-fold in pcDI-[12Asp]K-ras4B-NIH3T3 and 19-fold in HEC-1A. RafS621A suppressed the ER transcriptional activity.

Conclusions: K-ras mutation induces tumorigenesis in endometrium, and this malignant transformation involves Raf signaling pathway and ER.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Growth Processes / genetics
  • Endometrial Neoplasms / genetics*
  • Endometrial Neoplasms / metabolism
  • Female
  • Genes, Reporter
  • Genes, ras*
  • Humans
  • Luciferases / genetics
  • Mice
  • NIH 3T3 Cells
  • Plasmids / genetics
  • Point Mutation*
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Receptors, Estrogen / biosynthesis*
  • Receptors, Estrogen / genetics
  • Transcriptional Activation
  • Transfection
  • Up-Regulation
  • ras Proteins / genetics*

Substances

  • KRAS protein, human
  • Receptors, Estrogen
  • Luciferases
  • Proto-Oncogene Proteins p21(ras)
  • ras Proteins