Kiuru Maija, Lehtonen Rainer, Eerola Hannaleena, Aittomäki Kristiina, Blomqvist Carl, Nevanlinna Heli, Aaltonen Lauri A, Launonen Virpi
Department of Medical Genetics, Biomedicum Helsinki, University of Helsinki, P.O. Box 63 (Haartmaninkatu 8), FIN-00014 Helsinki, Helsinki, Finland.
Eur J Hum Genet. 2005 Apr;13(4):506-9. doi: 10.1038/sj.ejhg.5201326.
Fumarate hydratase: (FH) was recently identified as the predisposing gene for a tumor predisposition syndrome, hereditary leiomyomatosis and renal cell cancer (HLRCC) (MIM 605839). In HLRCC, individuals with a germline heterozygous mutation in the FH gene typically develop benign leiomyomas of the skin and the uterus (fibroids, myomas). In a subset of the families, predisposition to renal cell carcinoma and uterine leiomyosarcoma occurs. Other malignancies including breast cancer have also been detected in patients with a germline FH mutation. To examine whether FH could be involved in predisposition to breast cancer, we analyzed germline FH mutations from 85 Finnish breast cancer patients. Most of the cases were selected based on positive family or personal history for malignancies associated with HLRCC. No mutations were found. These results show that FH is not a major predisposing gene for familial breast cancer.
延胡索酸水合酶(FH)最近被确定为一种肿瘤易感性综合征——遗传性平滑肌瘤病和肾细胞癌(HLRCC,MIM 605839)的易感基因。在HLRCC中,FH基因发生种系杂合突变的个体通常会发展出皮肤和子宫的良性平滑肌瘤(纤维瘤、肌瘤)。在部分家族中,会出现肾细胞癌和子宫平滑肌肉瘤的易感性。在携带种系FH突变的患者中还检测到了包括乳腺癌在内的其他恶性肿瘤。为了研究FH是否可能与乳腺癌易感性有关,我们分析了85名芬兰乳腺癌患者的种系FH突变。大多数病例是根据与HLRCC相关的恶性肿瘤的阳性家族史或个人史选择的。未发现突变。这些结果表明,FH不是家族性乳腺癌的主要易感基因。