SDHD公司
SDHB系统
副神经节瘤
SDHA
嗜铬细胞瘤
种系突变
遗传学
生物
多发性内分泌肿瘤2型
癌症研究
基因
突变
医学
内分泌学
病理
基因表达
作者
Kazumasa Isobe,Shigeru Minowada,Ichiro Tatsuno,Kazumi Suzukawa,Sumiko Nissato,Toru Nanmoku,Hisato Hara,T Yäshiro,Yasushi Kawakami,Kazuhiro Takekoshi
摘要
The SDHA, SDHB, SDHC, and SDHD genes code for subunits of succinate dehydrogenase (SDH), which forms part of the mitochondrial respiratory chain. Germline mutations in the genes encoding SDHB and SDHD have been reported in familial paragangliomas/pheochromocytomas and in apparently sporadic pheochromocytomas. SDHB and SDHD mutations are widely distributed along the genes with no apparent hot spots. SDHB mutations are often detected in malignant and extra-adrenal pheochromocytomas. SDHD mutations are also detected frequently in head and neck paragangliomas. We sequenced the entire coding regions of the SDHB and SDHD genes in 17 pheochromocytomas. We identified novel heterozygous G to A point mutations at the first base of intron 3 of the SDHB gene in a malignant extra-adrenal abdominal pheochromocytoma patient, and at the first base of codon 111 of the SDHD gene in an adrenal pheochromocytoma patient. Further, we confirmed the SDHD mutation by DHPLC. The prevalence of SDHB and SDHD mutations in pheochromocytomas we examined was 12% (2/17). Thus, we identified two novel SDH mutations in Japanese pheochromocytomas. Further studies will investigate the oncogenic potential of these mutations.
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