CA 125 production and release by ovarian cancer cells in vitro

被引:18
作者
Beck, EP
Moldenhauer, A
Merkle, E
Kiesewetter, F
Jäger, W
Wildt, L
Lang, N
机构
[1] Stadt Frauenklin Berg, D-70190 Stuttgart, Germany
[2] Univ Erlangen Nurnberg, Dept Obstet & Gynecol, D-8520 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Dept Dermatol, D-8520 Erlangen, Germany
关键词
CA; 125; cell culture; cell cycle distribution analysis; ovarian cancer; cell growth;
D O I
10.1177/172460089801300405
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The antigenic determinant CA 125 is a high molecular weight glycoprotein which is elevated in more than 80% of patients with epithelial ovarian cancel: Despite its good performance as a human tumor marker; only little is known about its physiological function. According to recent publications, CA 125 production and release appear to be related to cellular growth. In order to investigate this putative relationship move closely we analyzed the pattern of CA 125 production and release by ovarian cancer cells during exponential cell growth, during cell cycle arrest by colchicine and during inhibition of cellular protein synthesis by cycloheximide. The results were correlated with the cell cycle distribution. According to our results, the main determinant of CA 125 release into the culture supernatant is the total cell count. Although cell cycle arrest in the G2 + M phase by means of colchicine treatment resulted in the death of most cells, which was reflected by an increased release of CA 125, no differences in the intracellular production rate between colchicine treated and untreated cells were seen. In contrast treatment of cells with cycloheximide not only resulted in decreasing cell numbers but also in a complete inhibition of CA 125 production by surviving cells.
引用
收藏
页码:200 / 206
页数:7
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