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日本嗜铬细胞瘤中SDHB和SDHD基因的新型种系突变。

Novel germline mutations in the SDHB and SDHD genes in Japanese pheochromocytomas.

作者信息

Isobe Kazumasa, Minowada Shigeru, Tatsuno Ichiro, Suzukawa Kazumi, Nissato Sumiko, Nanmoku Toru, Hara Hisato, Yashiro Toru, Kawakami Yasushi, Takekoshi Kazuhiro

机构信息

Department of Clinical Pathology, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan.

出版信息

Horm Res. 2007;68(2):68-71. doi: 10.1159/000099655. Epub 2007 Feb 15.

Abstract

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.

摘要

SDHA、SDHB、SDHC和SDHD基因编码琥珀酸脱氢酶(SDH)的亚基,SDH是线粒体呼吸链的一部分。据报道,编码SDHB和SDHD的基因发生种系突变与家族性副神经节瘤/嗜铬细胞瘤以及明显散发的嗜铬细胞瘤有关。SDHB和SDHD突变在基因中广泛分布,没有明显的热点。SDHB突变常出现在恶性和肾上腺外嗜铬细胞瘤中。SDHD突变也经常在头颈部副神经节瘤中被检测到。我们对17例嗜铬细胞瘤的SDHB和SDHD基因的整个编码区进行了测序。我们在一名恶性肾上腺外腹部嗜铬细胞瘤患者的SDHB基因内含子3的第一个碱基处,以及一名肾上腺嗜铬细胞瘤患者的SDHD基因第111密码子的第一个碱基处,鉴定出了新的杂合G到A点突变。此外,我们通过变性高效液相色谱法(DHPLC)证实了SDHD突变。在我们检测的嗜铬细胞瘤中,SDHB和SDHD突变的发生率为12%(2/17)。因此,我们在日本嗜铬细胞瘤中鉴定出了两个新的SDH突变。进一步的研究将调查这些突变的致癌潜力。

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