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肿瘤细胞在体外产生前列腺素E2。

Production of prostaglandin E2 by tumor cells in vitro.

作者信息

Owen K, Gomolka D, Droller M J

出版信息

Cancer Res. 1980 Sep;40(9):3167-71.

PMID:7427935
Abstract

Our previous observations on the production of prostaglandin E2 (PGE2) by bladder tumor cell lines in vitro and the enhancement of tumor cell PGE2 production upon exposure to purified peripheral blood lymphocytes from normal human donors prompted us to examine this interaction in an animal model in order to further define conditions that determine the occurrence of this phenomenon. Cell lines derived from carcinogen-induced bladder and mammary tumors and from embryo fibroblasts in Fischer rats were exposed to purified peripheral blood or splenic lymphocytes in the presence or absence of indomethacin (10(-7)M). After varying times at 37 degrees, supernatants were harvested for determination of PGE2 by radioimmunoassay. Time course studies demonstrated rapid PGE2 production with plateau levels appearing at 8 hr. Increased tumor cell PGE2 production occurred in the presence of increased numbers of lymphocytes. Indomethacin partially inhibited PGE2 production. Preincubation studies suggested that the contribution of lymphocytes to overall PGE2 production in the present system was minimal. On the basis of previous observations of PGE2-associated inhibition of lymphocyte cytotoxicity against tumor cells in vitro, the present results suggest that tumor cell PGE2 production may reflect a response of the tumor cells to challenge by effector lymphocytes and may represent a mechanism whereby tumor cells subvert an immune response mounted against them.

摘要

我们之前对膀胱肿瘤细胞系在体外产生前列腺素E2(PGE2)的观察,以及在接触来自正常人类供体的纯化外周血淋巴细胞后肿瘤细胞PGE2产生的增强,促使我们在动物模型中研究这种相互作用,以便进一步确定决定这种现象发生的条件。将源自致癌物诱导的膀胱和乳腺肿瘤以及费希尔大鼠胚胎成纤维细胞的细胞系,在存在或不存在吲哚美辛(10^(-7)M)的情况下,暴露于纯化的外周血或脾淋巴细胞。在37℃下经过不同时间后,收集上清液,通过放射免疫测定法测定PGE2。时间进程研究表明PGE2快速产生,在8小时出现平台期水平。淋巴细胞数量增加时,肿瘤细胞PGE2产生增加。吲哚美辛部分抑制PGE2产生。预孵育研究表明,在本系统中淋巴细胞对总体PGE2产生的贡献最小。基于之前在体外观察到PGE2对淋巴细胞针对肿瘤细胞的细胞毒性的抑制作用,目前的结果表明肿瘤细胞PGE2产生可能反映了肿瘤细胞对效应淋巴细胞攻击的反应,并且可能代表了肿瘤细胞颠覆针对它们的免疫反应的一种机制。

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