首页> 外文期刊>The American Journal of Human Genetics >Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes.
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Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes.

机译:Cowden和Cowden-like综合征的琥珀酸脱氢酶基因中的种系突变和变异。

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Individuals with PTEN mutations have Cowden syndrome (CS), associated with breast, thyroid, and endometrial neoplasias. Many more patients with features of CS, not meeting diagnostic criteria (termed CS-like), are evaluated by clinicians for CS-related cancer risk. Germline mutations in succinate dehydrogenase subunits SDHB-D cause pheochromocytoma-paraganglioma syndrome. One to five percent of SDHB/SDHD mutation carriers have renal cell or papillary thyroid carcinomas, which are also CS-related features. SDHB-D may be candidate susceptibility genes for some PTEN mutation-negative individuals with CS-like cancers. To address this hypothesis, germline SDHB-D mutation analysis in 375 PTEN mutation-negative CS/CS-like individuals was performed, followed by functional analysis of identified SDH mutations/variants. Of 375 PTEN mutation-negative CS/CS-like individuals, 74 (20%) had increased manganese superoxide dismutase (MnSOD) expression, a manifestation of mitochondrial dysfunction. Among these, 10 (13.5%) had germline mutations/variants in SDHB (n = 3) or SDHD (7), not found in 700 controls (p < 0.001). Compared to PTEN mutation-positive CS/CS-like individuals, those with SDH mutations/variants were enriched for carcinomas of the female breast (6/9 SDH versus 30/107 PTEN, p < 0.001), thyroid (5/10 versus 15/106, p < 0.001), and kidney (2/10 versus 4/230, p = 0.026). In the absence of PTEN alteration, CS/CS-like-related SDH mutations/variants show increased phosphorylation of AKT and/or MAPK, downstream manifestations of PTEN dysfunction. Germline SDH mutations/variants occur in a subset of PTEN mutation-negative CS/CS-like individuals and are associated with increased frequencies of breast, thyroid, and renal cancers beyond those conferred by germline PTEN mutations. SDH testing should be considered for germline PTEN mutation-negative CS/CS-like individuals, especially in the setting of breast, thyroid, and/or renal cancers.
机译:具有PTEN突变的个体患有Cowden综合征(CS),与乳房,甲状腺和子宫内膜瘤形成相关。临床医师评估了更多具有CS特征但不符合诊断标准的患者(称为CS样),以评估CS相关的癌症风险。琥珀酸脱氢酶亚基SDHB-D的种系突变导致嗜铬细胞瘤-副神经节瘤综合征。百分之一到百分之五的SDHB / SDHD突变携带者患有肾细胞癌或甲状腺乳头状癌,这也是与CS相关的特征。 SDHB-D可能是一些患有CS样癌症的PTEN突变阴性个体的候选易感基因。为了解决这个假设,对375个PTEN突变阴性的CS / CS样个体进行了种系SDHB-D突变分析,然后对鉴定出的SDH突变/变体进行功能分析。在375个PTEN突变阴性的CS / CS样个体中,有74个(20%)的锰超氧化物歧化酶(MnSOD)表达增加,这是线粒体功能障碍的一种表现。其中,有10个(13.5%)在SDHB(n = 3)或SDHD(7)中具有种系突变/变异,在700个对照中没有发现(p <0.001)。与PTEN突变阳性的CS / CS样个体相比,那些具有SDH突变/变体的个体在女性乳腺癌(6/9 SDH对30/107 PTEN,p <0.001),甲状腺(5/10对15)的癌症中富集/ 106,p <0.001)和肾脏(2/10对4/230,p = 0.026)。在没有PTEN改变的情况下,CS / CS样相关的SDH突变/变体显示AKT和/或MAPK的磷酸化增加,这是PTEN功能障碍的下游表现。生殖系SDH突变/变异发生在PTEN突变阴性的CS / CS样个体中,并且与乳腺癌,甲状腺癌和肾癌的发生频率增加有关,超过了生殖系PTEN突变所赋予的频率。对于种系PTEN突变阴性的CS / CS样个体,应考虑SDH检测,尤其是在乳腺癌,甲状腺癌和/或肾癌的情况下。

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