EFFECTS OF TRANSFORMING GROWTH-FACTORS AND REGULATION OF THEIR MESSENGER-RNA LEVELS IN 2 HUMAN ENDOMETRIAL ADENOCARCINOMA CELL-LINES
EFFECTS OF TRANSFORMING GROWTH-FACTORS AND REGULATION OF THEIR MESSENGER-RNA LEVELS IN 2 HUMAN ENDOMETRIAL ADENOCARCINOMA CELL-LINES
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DOI：
10.1016/0960-0760(92)90256-i
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发表时间：
1992-06-01
影响因子：
4.1
通讯作者：
GURPIDE, E
中科院分区：
文献类型：
--
作者：
ANZAI, Y;GONG, YW;GURPIDE, E
The effects of the transforming growth factor-beta-1 (TGF-beta-1) and epidermal growth factor (EGF) on the growth of cells from 2 endometrial cancer lines, Ishikawa and HEC-50 were evaluated by measuring rates of DNA synthesis and changes in cell numbers during culture. EGF at 17 and 1.7 nM concentrations consistently enhanced HEC-50 cell proliferation. TGF-beta-1 inhibited Ishikawa cell proliferation but, unexpectedly for epithelium-derived cells, stimulated HEC-50 cell growth. This effect is of interest as it indicates that endometrial cells can acquire an altered responsiveness to a growth inhibitor during the process of malignant transformation. Northern blot analyses showed expression of TGF-alpha, TGF-beta-1 and EGF receptors mRNA in both cell lines. Neither estradiol (E2) nor 4-hydroxytamoxifen (OHTam) affected mRNA levels for either TGF-alpha or TGF-beta in HEC-50 cells, a line unresponsive to E2 for proliferation. In Ishikawa cells, previously shown to respond to both E2 and OHTam by increasing proliferation rates, E2 increased TGF-alpha mRNA and reduced TGF-beta mRNA levels. OHTam lowered the levels of both mRNA species, although the effect was greater on TGF-beta than TGF-alpha mRNA. These data are consistent with, but do not prove, the existence of a possible autocrine regulation by TGF-alpha and TGF-beta of human cancer cell proliferation, which might be under E2 influence in Ishikawa cells.
