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不同性激素对 NNK 解毒的抑制作用不同:可能是性别特异性肺癌风险的一个解释。

Different inhibitory potential of sex hormones on NNK detoxification in vitro: A possible explanation for gender-specific lung cancer risk.

机构信息

Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Campus Kiel, Brunswiker Str. 10, 24105 Kiel, Germany.

Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Campus Kiel, Brunswiker Str. 10, 24105 Kiel, Germany.

出版信息

Cancer Lett. 2017 Oct 1;405:120-126. doi: 10.1016/j.canlet.2017.07.016. Epub 2017 Jul 22.

Abstract

Smoking women are probably at a higher risk to develop lung cancer than men. Different explanations exist for these findings, a gender-specific impairment of tobacco carcinogen metabolism being one of them. In this study, we examined the inhibition of NNK reduction to NNAL, the first and most important detoxication step of this tobacco-specific carcinogen. It is mediated by different carbonyl reductases of the SDR (CBR1 and 11βHSD1) and AKR (AKR1B10, AKR1C1, AKR1C2 and AKR1C4) superfamilies. Inhibition constants of NNK reduction were determined with male (testosterone) and female (estradiol, progesterone) sex hormones and the contraceptives ethinylestradiol and drospirenone in A549 cells and with purified enzymes. Female sex hormones turned out to be stronger inhibitors than testosterone. The gestagen progesterone and its synthetic derivative drospirenone are the strongest inhibitors with K-values similar to hormone levels in pregnant women or women using hormonal contraceptives. Therefore, pregnancy or hormonal contraception may commit these women as high risk groups. The results of this study support the hypothesis that women bear a higher lung cancer risk when smoking because of female sex hormones acting as inhibitors of NNK detoxication.

摘要

吸烟的女性比男性更容易患肺癌。这些发现有不同的解释,其中之一是烟草致癌物质代谢的性别特异性损伤。在这项研究中,我们研究了 NNK 还原为 NNAL 的抑制作用,这是该烟草特异性致癌物的第一个也是最重要的解毒步骤。它由 SDR(CBR1 和 11βHSD1)和 AKR(AKR1B10、AKR1C1、AKR1C2 和 AKR1C4)超家族的不同羰基还原酶介导。我们在 A549 细胞和纯化酶中用男性(睾丸激素)和女性(雌二醇、孕酮)性激素以及避孕药炔雌醇和屈螺酮测定了 NNK 还原的抑制常数。女性性激素比睾丸激素的抑制作用更强。孕激素孕酮及其合成衍生物屈螺酮是最强的抑制剂,其 K 值与孕妇或使用激素避孕药的女性体内的激素水平相似。因此,怀孕或激素避孕药可能会使这些女性成为高风险群体。这项研究的结果支持了这样的假设,即女性吸烟时患肺癌的风险更高,因为女性性激素作为 NNK 解毒的抑制剂发挥作用。

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