首页> 外文期刊>Acta oncologica. >Glucose-6-phosphate dehydrogenase deficiency reduces susceptibility to cancer of endodermal origin
【24h】

Glucose-6-phosphate dehydrogenase deficiency reduces susceptibility to cancer of endodermal origin

机译:葡萄糖-6-磷酸脱氢酶缺乏减少了对内胚层血症癌症的敏感性

获取原文
获取原文并翻译 | 示例
           

摘要

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited enzyme defect worldwide. There is a growing scientific evidence for a protective role of G6PD deficiency against carcinogenesis. In this retrospective analysis, we tested the hypothesis that G6PD deficiency may reduce the risk of developing cancer in a tissue-specific manner. Material and methods: The study was conducted using data from 11,708 subjects undergoing gastrointestinal endoscopic procedures between 2002 and 2018 and tested for G6PD status in a teaching hospital of Northern Sardinia, Italy. Results: A 40% reduction of risk for cancer of endodermal origin was observed among G6PD-deficient patients compared with subjects with normal enzyme activity (relative risk (RR) 0.61, 95% confidence interval (Cl) 0.47-0.80) in both genders, confirmed by multivariable generalized linear regression after adjusting for age, sex, smoking habits, body mass index, diabetes and socio-economic status. The 'protective' effect of G6PD deficiency was larger for gastric cancer (RR 0.41, 95% Cl 0.18-0.99), hepato-cellular carcinoma (RR 0.48, 95% Cl 0.26-0.92) and colorectal cancer (RR 0.72, 95% Cl 0.53-0.98), while a non-significant risk was observed for breast, prostate, lung, hematopoietic and metastases (primary site unknown). Conclusions: Our results suggest a reduced susceptibility to develop cancers, mostly of endodermal origin (stomach, colon and liver), but not of ectodermal/mesodermal origin, in carriers of G6PD deficiency. The effects of G6PD deficiency on carcinogenesis need further studies to better understand how cancer cells originating from different germ layers use pentose phosphate pathway to proliferate.
机译:背景:葡萄糖-6-磷酸脱氢酶(G6PD)缺乏是全球最常见的遗传酶缺陷。 G6PD缺乏对致癌作用的保护作用,存在日益增长的科学证据。在此回顾性分析中,我们测试了G6PD缺乏可能降低组织特异性癌症的风险的假设。材料和方法:使用来自2002年至2018年的11,708名受试者的数据进行了研究,并在意大利北部撒丁岛教学医院进行了G6PD地位测试。结果:与具有正常酶活性的受试者相比,G6PD缺陷患者(相对风险(RR)0.61,95%置信区间(CL)0.47-0.80)中的受试者在两种性别中观察到40%的癌症癌症风险降低了40%的癌症癌症的风险降低在调整年龄,性别,吸烟习惯,体重指数,糖尿病和社会经济地位后,通过多变量广义线性回归证实。 G6PD缺乏的保护效果较大,对于胃癌(RR 0.41,95%Cl 0.18-0.99),肝细胞癌(RR 0.48,95%Cl 0.26-0.92)和结直肠癌(RR 0.72,95%Cl 0.53-0.98),乳腺癌,前列腺,肺,造血和转移(主要场地未知)观察到非重大风险。结论:我们的结果表明,显性易感性降低,大多数是内胚层源(胃,结肠和肝脏),但不是异端/中胚层,在G6PD缺乏的携带者中。 G6PD缺乏对致癌作用的影响需要进一步的研究以更好地了解源自不同胚层的癌细胞如何使用戊糖磷酸途径来增殖。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号