## Abstract Spontaneously immortalized human mammary epithelial cells MCF‐IOA were transfected with an activated c‐Ha‐ras oncogene. Transfected cells (MCF‐IOT) acquire a malignant pheno‐type, as already reported. Studies of l‐2′‐deoxyuridine incorporation in cultures given graded doses of hydrocort
Pretreatment with vitamin A inhibits transforming growth factor alpha stimulation of human mammary carcinoma cells
✍ Scribed by Susan A. Halter; Angela R. Winnier; Carlos L. Arteaga
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 944 KB
- Volume
- 156
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Vitamin A or retinol is an important agent in the normal differentiation and growth of cells. Retinol is an effective inhibitor of the growth of many transformed cells in vitro and in vivo but its mechanism of action is unclear. Transforming growth factor alpha (TGFa) is a known mitogen. We examined the effect of retinol treatment on TGFa stimulation of two human mammary carcinoma cell lines, one which is growth inhibited by retinol and one which is not. Pretreatment of both cell lines for 48 hours with retinol resulted in inhibition of TCFa stimulation of growth. In the T47D cell line the mechanism was not related to an effect on the cellular content of TGFa, epidermal growth factor (ECF) receptor protein, EGF receptor mRNA, or on the binding of TGFa to the EGF receptor. However, TGFa-induced stimulation of the EGF receptor substrate, phospholipase C-yl , was abrogated in the T47D cell line with retinol pretreatment. In the MDA-MB-468 cell line, pretreatment with retinol resulted in a decrease in tyrosine phosphorylation of the ECF receptor. These results suggest that pretreatment with retinol decreases cellular proliferation seen with TGFa treatment by altering phospholipase C-yl response and/or ECF receptor tyrosine kinase activity. Alteration of phospholipase C-yl activity does not appear to be responsible for the inhibition of cell growth seen in the absence of TGFa stimulation. o 1993 ~i l e y -~i s s , Inc.
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## Abstract The effects of EGF and TGF‐β1 on the proliferation of 2 ovarian carcinoma cell lines (IGROV1 and OVCCR1) were evaluated. The cell lines were adapted to grow in a restricted serum (0.5%) medium. EGF was required for proliferation of both ovarian cell lines. Low doses of TGF‐β1 inhibited