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雌激素对人卵巢癌细胞中c-myc原癌基因的转录激活作用。

Transcriptional activation of c-myc proto-oncogene by estrogen in human ovarian cancer cells.

作者信息

Chien C H, Wang F F, Hamilton T C

机构信息

Department and Institute of Biochemistry, National Yang-Ming Medical College, Shih Pai, Taipei, Taiwan.

出版信息

Mol Cell Endocrinol. 1994 Feb;99(1):11-9. doi: 10.1016/0303-7207(94)90140-6.

Abstract

NIH

OVCAR-3 is a human ovarian cancer cell line that expresses a moderate amount of estrogen receptors, 28 fmol/mg protein. We have found that estrogen at a concentration of 10(-7) M induced a 2.3-fold increase in the growth of NIH:OVCAR-3 cells after 48 h stimulation. A 4-fold increase in c-myc mRNA expression at 30 min and a 7.5-fold increase at 50 min post-induction with estradiol were observed. Nuclear run-on analysis indicated that c-myc transcripts increased 4-fold within 10 min of estrogen addition. The half-life of c-myc mRNA was 64 min +/- 5 min and was not affected by estrogen. Antisense oligonucleotide to c-myc specifically inhibited the estrogen stimulated c-myc protein expression as well as the growth of NIH:OVCAR-3 cells. A control ovarian cancer cell line OC-3-VGH that had few estrogen receptors (1 fmol/mg protein) did not respond to estrogen in growth; however, these cells respond to estrogen with a 1.5-fold increase in c-myc mRNA. The stability of c-myc mRNA of these cells was not affected by estrogen. Our results indicate that transcriptional induction of c-myc expression by estrogen plays a critical role in the proliferation of NIH:OVCAR-3 cells.

摘要

美国国立卫生研究院

NIH:OVCAR-3是一种人卵巢癌细胞系,表达中等量的雌激素受体,为28飞摩尔/毫克蛋白。我们发现,在10(-7)M浓度的雌激素刺激48小时后,NIH:OVCAR-3细胞的生长增加了2.3倍。用雌二醇诱导后30分钟时c-myc mRNA表达增加4倍,50分钟时增加7.5倍。核转录分析表明,添加雌激素后10分钟内c-myc转录本增加4倍。c-myc mRNA的半衰期为64分钟±5分钟,不受雌激素影响。针对c-myc的反义寡核苷酸特异性抑制雌激素刺激的c-myc蛋白表达以及NIH:OVCAR-3细胞的生长。雌激素受体较少(1飞摩尔/毫克蛋白)的对照卵巢癌细胞系OC-3-VGH在生长方面对雌激素无反应;然而,这些细胞对雌激素的反应是c-myc mRNA增加1.5倍。这些细胞中c-myc mRNA的稳定性不受雌激素影响。我们的结果表明,雌激素对c-myc表达的转录诱导在NIH:OVCAR-3细胞的增殖中起关键作用。

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