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维甲酸和抗雌激素对人乳腺癌细胞周期进程及细胞周期调控基因的不同影响。

Differential effects of retinoids and antiestrogens on cell cycle progression and cell cycle regulatory genes in human breast cancer cells.

作者信息

Wilcken N R, Sarcevic B, Musgrove E A, Sutherland R L

机构信息

Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst, NSW, Australia.

出版信息

Cell Growth Differ. 1996 Jan;7(1):65-74.

PMID:8788034
Abstract

Retinoids have antiproliferative effects in human breast cancer cells and share some characteristics with antiestrogens, although the molecular targets involved have yet to be identified in either case. Using T-47D human breast cancer cells, we compared the effects of retinoic acid (RA) and the antiestrogen ICI 164384 on cell cycle phase distribution and the expression of genes with known functions in cell cycle control. Both RA and ICI 164384 inhibited cell cycle progression in G1 phase, but the RA effect was delayed by 16 h. This delay in action was also seen with 9-cis RA and other retinoids. Administration of 17 beta-estradiol abolished the effects of ICI 164384 but was without effect in RA-treated cells. Antiestrogen treatment caused a rapid inhibition of c-myc and cyclin D1 gene expression and reduced Cdk2 activity by more than 50% at 24 h. RA, however, did not affect c-myc or cyclin D1 gene expression, nor did it significantly change the mRNA or protein levels of cyclins D3 or E or cyclin-dependent kinases (CDK) Cdk2 or Cdk4. RA-induced reduction in Cdk2 activity was modest and occurred after %S phase declined, while Cdk4 activity was reduced, coincident with cell cycle changes. However, following either RA or ICI 164384, there was a reduction in the amount of hyperphosphorylated pRB, first apparent well before cell cycle changes were seen. These data demonstrate that: (a) the mechanisms of action of antiestrogens and retinoids are different but converge at pRB; and (b) RA can affect CDK activity without reducing cyclin or CDK levels.

摘要

维甲酸在人乳腺癌细胞中具有抗增殖作用,并且与抗雌激素有一些共同特征,尽管在这两种情况下所涉及的分子靶点均尚未确定。我们使用T-47D人乳腺癌细胞,比较了视黄酸(RA)和抗雌激素ICI 164384对细胞周期阶段分布以及细胞周期调控中已知功能基因表达的影响。RA和ICI 164384均抑制G1期的细胞周期进程,但RA的作用延迟了16小时。9-顺式RA和其他维甲酸也出现了这种作用延迟。给予17β-雌二醇可消除ICI 164384的作用,但对RA处理的细胞无效。抗雌激素处理可迅速抑制c-myc和细胞周期蛋白D1基因的表达,并在24小时时使Cdk2活性降低超过50%。然而,RA并不影响c-myc或细胞周期蛋白D1基因的表达,也未显著改变细胞周期蛋白D3或E、细胞周期蛋白依赖性激酶(CDK)Cdk2或Cdk4的mRNA或蛋白质水平。RA诱导的Cdk2活性降低较为适度,且在S期下降后才出现,而Cdk4活性降低与细胞周期变化同步。然而,在给予RA或ICI 164384后,高磷酸化pRB的量均减少,这在细胞周期变化出现之前就已明显可见。这些数据表明:(a)抗雌激素和维甲酸的作用机制不同,但在pRB处汇聚;(b)RA可在不降低细胞周期蛋白或CDK水平的情况下影响CDK活性。

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