δ 12-前列腺素J2增强重组人肿瘤坏死因子的抗增殖活性。

H Mori, Y Takada, H Kondoh, T Tamaya
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引用次数: 0

摘要

研究肿瘤坏死因子(tumor necrosis factor, TNF)和环戊酮前列腺素(cyclopentenone prostaglandins, PGA2和δ 12-PGJ2)单独或联合使用对3种人妇科肿瘤细胞系(HeLa S3、HHUA和CAOV-3)体外增殖的影响。HeLa S3和CAOV-3细胞对TNF无反应,HHUA细胞对TNF表现出最低程度的反应。HeLa S3和HHUA细胞对PGA2呈剂量依赖性反应,CAOV-3细胞对PGA2有轻微反应。所有三种细胞系都对δ 12-PGJ2高度敏感。TNF和δ 12-PGJ2在三种细胞系中均表现出协同抗增殖作用。δ 12-PGJ2预处理增强了TNF在这些细胞系中的有效性,反之则不然。在这三种细胞系中,TNF和PGA2之间不存在协同相互作用。这些结果表明,TNF和δ 12-PGJ2联合治疗可以在临床试验中提供一种获得更高疗效的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Augmentation of antiproliferative activity of recombinant human tumor necrosis factor by delta 12-prostaglandin J2.

The effects of tumor necrosis factor (TNF) and cyclopentenone prostaglandins (PGA2 and delta 12-PGJ2), singly and in combination, against proliferation in three human gynecologic tumor cell lines (HeLa S3, HHUA, and CAOV-3) were examined in vitro. The HeLa S3 and CAOV-3 cells were unresponsive to TNF, and the HHUA cells exhibited a minimal degree of responsiveness to TNF. The HeLa S3 and HHUA cells were responsive dose-dependently to PGA2, and the CAOV-3 cells were slightly responsive to PGA2. All three cell lines were highly responsive to delta 12-PGJ2. The synergistic antiproliferative effect of TNF and delta 12-PGJ2 appeared in all three cell lines. Pretreatment with delta 12-PGJ2 enhanced the effectiveness of TNF in these cell lines, but not vice versa. A synergistic interaction between TNF and PGA2 was absent in these three cell lines. These results suggest that a combined treatment with TNF and delta 12-PGJ2 could provide a new approach to obtaining increased responses in clinical trials.

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