Appelqvist Frida, Yhr Maria, Erlandson Anna, Martinsson Tommy, Enerbäck Charlotta
Department of Dermatology, Institute of Clinical Sciences, Sahlgrenska University Hospital, SE-413 45, Göteborg, Sweden.
Genes Chromosomes Cancer. 2014 Aug;53(8):703-11. doi: 10.1002/gcc.22180. Epub 2014 May 6.
The DNA repair gene MGMT (O-6-methylguanine-DNA methyltransferase) is important for maintaining normal cell physiology and genomic stability. Alterations in MGMT play a critical role in the development of several types of cancer, including glioblastoma, lung cancer, and colorectal cancer. The purpose of this study was to explore the function of genetic alterations in MGMT and their connection with familial melanoma (FM). Using multiplex ligation-dependent probe amplification, we identified a deletion that included the MGMT gene in one of 64 families with a melanoma predisposition living in western Sweden. The mutation segregated with the disease as a heterozygous deletion in blood-derived DNA, but a homozygous deletion including the promoter region and exon 1 was seen in tumor tissue based on Affymetrix 500K and 6.0 arrays. By sequence analysis of the MGMT gene in the other 63 families with FM from western Sweden, we identified four common polymorphisms, nonfunctional, as predominantly described in previous studies. We conclude that inherited alterations in the MGMT gene might be a rare cause of FM, and we suggest that MGMT contributes to melanoma predisposition.
DNA修复基因MGMT(O-6-甲基鸟嘌呤-DNA甲基转移酶)对于维持正常细胞生理和基因组稳定性至关重要。MGMT的改变在包括胶质母细胞瘤、肺癌和结直肠癌在内的几种癌症的发生发展中起着关键作用。本研究的目的是探讨MGMT基因改变的功能及其与家族性黑色素瘤(FM)的关系。使用多重连接依赖探针扩增技术,我们在瑞典西部64个有黑色素瘤易感性的家族中的一个家族中鉴定出一个包含MGMT基因的缺失。该突变在血液来源的DNA中作为杂合缺失与疾病共分离,但基于Affymetrix 500K和6.0芯片,在肿瘤组织中发现了一个包括启动子区域和外显子1的纯合缺失。通过对瑞典西部另外63个FM家族的MGMT基因进行序列分析,我们鉴定出四种常见的多态性,如先前研究中主要描述的那样无功能。我们得出结论,MGMT基因的遗传改变可能是FM的罕见病因,并且我们认为MGMT促成了黑色素瘤易感性。