MDM2 enhances the function of estrogen receptor in human breast cancer cells

Shigehira Saji, Naoki Okumura, Hidetaka Eguchi, Shigeru Nakashima, Akio Suzuki, Masakazu Toi, Yoshinori Nozawa, Shigetoyo Saji, Shin ichi Hayashi

研究成果: Article査読

83 被引用数 (Scopus)

抄録

Overexpression of the oncoprotein MDM2, a negative feedback regulator of p53, is often observed in breast cancer tissue and cell lines, particularly in those which express estrogen receptor α (ERα). In this study, we report a novel function of MDM2, i.e., as a positive regulator of ERα. This function does not involve p53. MDM2 overexpressing clones derived from the breast cancer cell line, MCF-7 cells, showed a remarkable growth advantage only in estradiol supplemented conditions, and this profile coincided with increased transcriptional activity of ERa in these cells. Though p53 has been reported to be an inhibitor of ERα function, p53 protein in MDM2 overexpressing clones was more abundant than in the parental cells. When ERα was exogenously expressed in p53-null cells, its activity was enhanced by coexpression of MDM2. Mammalian two-hybrid assays and GST pull-down assays indicated that MDM2 could interact with ERα. These results indicate that MDM2 is a direct activator of ERα function, and suggest such a role for MDM2 in ERα-positive breast cancer.

本文言語English
ページ(範囲)259-265
ページ数7
ジャーナルBiochemical and biophysical research communications
281
1
DOI
出版ステータスPublished - 2001
外部発表はい

ASJC Scopus subject areas

  • 生物理学
  • 生化学
  • 分子生物学
  • 細胞生物学

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