Effect of modifiers of arachidonic acid metabolism on radiation transformation and eicosanoid formation in C3H/10T1/2 cells.

Cancer biochemistry biophysics Pub Date : 1994-10-01
P C Billings, P A Maki, A R Kennedy
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Abstract

In these studies, we performed experiments designed to elucidate the role that arachidonic acid metabolism plays in oncogenic transformation in vitro. The levels of TxB2 and 6-keto-PGF1 alpha were elevated in cells treated with X-rays. A significant increase in the levels of these eicosanoids was observed following irradiation. Treatment of cells with the anticarcinogenic protease inhibitors, Bowman-Birk Inhibitor (BBI) and N-tosyl-L-phenylalanine chloromethyl ketone (TPCK), significantly reduced the levels of TxB2 and 6-keto-PGF1 alpha present. Indomethacin treatment significantly reduced the levels of TxB2 and 6-keto-PGF1 alpha to < 10% of those present in untreated or irradiated cells. We also report that addition of lipoxygenase or minoxidil [a selective inhibitor of prostacyclin (PGl2) synthetase] led to a highly significant decrease in transformation. In addition, minoxidil treatment resulted in a significant reduction in the levels of 6-keto-PGF1 alpha in irradiated cells. Our results suggest the hypothesis that the relative levels of 6-keto-PGF1 alpha are important in radiation induced transformation.

花生四烯酸代谢调节剂对C3H/10T1/2细胞辐射转化和类二十烷形成的影响。
在这些研究中,我们进行了旨在阐明花生四烯酸代谢在体外致癌转化中的作用的实验。在x射线处理的细胞中,TxB2和6-keto-PGF1 α水平升高。辐照后观察到这些类二十烷酸的水平显著增加。用抗癌蛋白酶抑制剂Bowman-Birk Inhibitor (BBI)和n- toyl - l-苯丙氨酸氯甲基酮(TPCK)处理细胞,可显著降低TxB2和6-keto-PGF1 α的水平。吲哚美辛治疗显著降低TxB2和6-酮- pgf1 α水平,低于未治疗或辐照细胞的10%。我们还报道,添加脂氧合酶或米诺地尔(一种前列环素(PGl2)合成酶的选择性抑制剂)导致转化显著减少。此外,米诺地尔治疗导致辐照细胞中6-酮- pgf1 α水平显著降低。我们的研究结果表明,6-酮- pgf1 α的相对水平在辐射诱导转化中很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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