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地塞米松对OVCA 433卵巢癌细胞生长及表皮生长因子受体表达的影响。

Effects of dexamethasone on the growth and epidermal growth factor receptor expression of the OVCA 433 ovarian cancer cells.

作者信息

Ferrandina G, Scambia G, Benedetti Panici P, Bonanno G, De Vincenzo R, Rumi C, Bussa S, Genuardi M, Romano Spica V, Mancuso S

机构信息

Department of Obstetrics and Gynecology, Catholic University, Rome, Italy.

出版信息

Mol Cell Endocrinol. 1992 Feb;83(2-3):183-93. doi: 10.1016/0303-7207(92)90158-3.

Abstract

We studied the correlation between dexamethasone (Dex) induced growth effects and modulation of epidermal growth factor receptor (EGFR) expression in OVCA 433 ovarian cancer cells. These cells express specific high and low affinity 125I-EGF binding sites and are growth stimulated by EGF. Dex exhibits mitoinhibitory effects by recruiting OVCA 433 cells in the G0-G1 phase of the cycle, but increases the number of both the high and the low affinity EGFR in a dose dependent manner. The maximal EGFR expression increase occurs after 24 h of Dex treatment consistently with Northern blot studies. The mitogenic activity of EGF in OVCA 433 cells is not affected by the presence of Dex. Moreover Dex growth inhibition occurs in JA1 cells, an ovarian cancer cell line which expresses unfunctional EGFR and which is unresponsive to EGF. Our results indicate that the Dex induced growth effects occur independently of EGFR expression.

摘要

我们研究了地塞米松(Dex)诱导的生长效应与表皮生长因子受体(EGFR)在OVCA 433卵巢癌细胞中表达调节之间的相关性。这些细胞表达特异性的高亲和力和低亲和力125I-EGF结合位点,并受到EGF的生长刺激。Dex通过使OVCA 433细胞进入细胞周期的G0-G1期而表现出有丝分裂抑制作用,但以剂量依赖方式增加高亲和力和低亲和力EGFR的数量。与Northern印迹研究一致,Dex处理24小时后EGFR表达增加达到最大值。Dex的存在不影响EGF在OVCA 433细胞中的促有丝分裂活性。此外,Dex对JA1细胞有生长抑制作用,JA1细胞是一种表达无功能EGFR且对EGF无反应的卵巢癌细胞系。我们的结果表明,Dex诱导的生长效应独立于EGFR表达而发生。

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