首页> 外文期刊>Oncogene >Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
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Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

机译:家族性嗜铬细胞瘤和副神经节瘤中的新型琥珀酸脱氢酶亚基B(SDHB)突变,但散发性嗜铬细胞瘤中没有体细胞SDHB突变

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Phaeochromocytomas arising in adrenal or extra-adrenal sites and paragangliomas of the head and neck, in particular of the carotid bodies, occur sporadically and also in a familial setting. In addition to mutations in RET and VHL in familial disease, germline mutations in SDHD and SDHB genes that encode subunits of mitochondrial complex II have also been associated with the development of familial phaeochromocytomas. To further investigate the role of SDHD and SDHB in the development of these tumours we determined the occurrence of germline SDHD and SDHB mutations in four patients with a family history of phaeochromocytoma with associated head and neck paraganglioma, one patient with a family history of phaeochromocytoma only and two patients with apparently sporadic extra-adrenal phaeochromocytoma, one of whom had early onset disease. Secondly, we investigated whether somatic SDHB mutations correlated with loss of heterozygosity at 1p36 in a subgroup of 11 sporadic and three MEN 2-associated RET-mutation-positive phaeochromocytomas. Novel SDHB mutations were identified in the probands from four families and two apparently sporadic cases (six of seven probands studied), including two missense mutations, a single nonsense and frameshift mutation, as well as two splice site mutations, one of which was shown to have partial penetrance resulting in 'leaky' splicing. Further, five intronic polymorphisms in SDHB were found. No SDHD mutations were identified. In addition, no somatic SDHB mutations were found in the remaining allele of the 11 sporadic adrenal phaeochromocytomas with allelic loss at 1p36 or the three MEN 2-associated RET-mutation-positive phaeochromocytomas. Therefore, we conclude that SDHB has a major role in the pathogenesis of familial phaeochromocytomas, but the possible role of SDHB in sporadic tumours showing allelic loss at 1p36 has yet to be ascertained.
机译:发生在肾上腺或肾上腺外部位以及头部和颈部,特别是颈动脉体的神经节旁的嗜铬细胞瘤偶发,也发生在家族中。除了家族性疾病的RET和VHL突变外,编码线粒体复合体II亚基的SDHD和SDHB基因的种系突变也与家族性嗜铬细胞瘤的发生有关。为了进一步研究SDHD和SDHB在这些肿瘤发生中的作用,我们确定了4名伴有嗜铬细胞瘤家族史并伴有头颈部副神经节瘤的患者中,SDHD和SDHB突变发生的情况,其中1名仅伴有嗜铬细胞瘤家族史的患者2例患有偶发性肾上腺嗜铬细胞瘤的患者,其中1例发病较早。其次,我们调查了11个零星和3个与MEN 2相关的RET突变阳性的嗜铬细胞瘤的亚组中,体细胞SDHB突变是否与1p36杂合性丧失相关。在四个家族的先证者中发现了新的SDHB突变,两个显然是零星的病例(研究的七个先证者中有六个),包括两个错义突变,一个废话和移码突变,以及两个剪接位点突变,其中一个表明局部渗透,导致“漏缝”拼接。此外,在SDHB中发现了五个内含子多态性。没有发现SDHD突变。另外,在11个散发性肾上腺嗜铬细胞瘤的其余等位基因中,在1p36时等位基因丢失或三个与MEN 2相关的RET突变阳性的嗜铬细胞瘤的其余等位基因中未发现体细胞SDHB突变。因此,我们得出结论,SDHB在家族性嗜铬细胞瘤的发病机理中具有重要作用,但尚未确定SDHB在散发性肿瘤中在1p36等位基因丢失的可能作用。

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