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人子宫内膜HEC-1A癌细胞中内皮素-1基因的表达与生物合成

Endothelin-1 gene expression and biosynthesis in human endometrial HEC-1A cancer cells.

作者信息

Economos K, MacDonald P C, Casey M L

机构信息

Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas 75235-9051.

出版信息

Cancer Res. 1992 Feb 1;52(3):554-7.

PMID:1732042
Abstract

In this study, evidence was obtained that endothelin-1 (ET-1) is produced by an established endometrial cancer (HEC-1A) cell line. PreproET-1 mRNA is present in HEC-1A cells, and immunoreactive endothelin is secreted into the medium of these cells maintained in culture. Cycloheximide treatment of these cells caused superinduction of preproET-1 mRNA. Transforming growth factor-beta acts in these cells to increase the levels of preproET-1 mRNA. This effect of transforming growth factor-beta on preproET-1 mRNA accumulation was accompanied by an increase in the amount of immunoreactive endothelin secreted into the culture medium. ET-1, added to the culture medium, did not act as a mitogen in HEC-1A cells. We speculate that ET-1 (which is known to stimulate fibroblast proliferation) produced by endometrial adenocarcinoma cells may participate in the angiogenic process that occurs during the establishment of this carcinoma in vivo.

摘要

在本研究中,已获得证据表明,人子宫内膜癌(HEC-1A)细胞系可产生内皮素-1(ET-1)。前内皮素原-1(PreproET-1)mRNA存在于HEC-1A细胞中,且免疫反应性内皮素分泌到培养的这些细胞的培养基中。用放线菌酮处理这些细胞会导致前内皮素原-1 mRNA超诱导。转化生长因子-β在这些细胞中发挥作用,以增加前内皮素原-1 mRNA的水平。转化生长因子-β对前内皮素原-1 mRNA积累的这种作用伴随着分泌到培养基中的免疫反应性内皮素量的增加。添加到培养基中的ET-1在HEC-1A细胞中并不作为有丝分裂原起作用。我们推测,子宫内膜腺癌细胞产生的ET-1(已知可刺激成纤维细胞增殖)可能参与了该癌在体内形成过程中发生的血管生成过程。

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