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谷胱甘肽S-转移酶GSTM1表型与皮肤肿瘤的防护

Glutathione S-transferase GSTM1 phenotypes and protection against cutaneous tumours.

作者信息

Heagerty A H, Fitzgerald D, Smith A, Bowers B, Jones P, Fryer A A, Zhao L, Alldersea J, Strange R C

机构信息

Department of Dermatology, North Staffordshire Hospital, Stoke on Trent, UK.

出版信息

Lancet. 1994 Jan 29;343(8892):266-8. doi: 10.1016/s0140-6736(94)91115-0.

Abstract

Multiple allelism at loci encoding detoxicating enzymes is associated with cancer risk. We have studied genetic variation at the glutathione S-transferase GSTM1 locus to see whether phenotypes confer altered susceptibility to basal cell carcinoma (BCC), squamous cell carcinoma (SCC), malignant melanoma (MM), or multiple skin tumours of different histological types. The frequency of GSTM1 null in cases and controls (52%) was similar, except for patients with two or more tumours of different types (71%, p = 0.033). GSTM1 A/B was reduced in frequency (p < 0.05) in patients with single or multiple BCC. Thus GSTM1 A/B may be protective, and effectiveness of detoxication may be a factor determining susceptibility to skin cancer.

摘要

编码解毒酶的基因座上的多个等位基因与癌症风险相关。我们研究了谷胱甘肽S-转移酶GSTM1基因座的遗传变异,以观察其表型是否会改变对基底细胞癌(BCC)、鳞状细胞癌(SCC)、恶性黑色素瘤(MM)或不同组织学类型的多发性皮肤肿瘤的易感性。病例组和对照组中GSTM1基因缺失的频率(52%)相似,但患有两种或更多不同类型肿瘤的患者中该频率为71%(p = 0.033)。在单发或多发BCC患者中,GSTM1 A/B的频率降低(p < 0.05)。因此,GSTM1 A/B可能具有保护作用,解毒效果可能是决定皮肤癌易感性的一个因素。

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