Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes

被引:154
作者
Ni, Ying [1 ,2 ,3 ]
Zbuk, Kevin M. [1 ,2 ]
Sadler, Tammy [1 ,2 ]
Patocs, Attila [1 ,2 ]
Lobo, Glenn [1 ,2 ]
Edelman, Emily [1 ,2 ,4 ]
Platzer, Petra [1 ,2 ]
Orloff, Mohammed S. [1 ,2 ,4 ]
Waite, Kristin A. [1 ,2 ,4 ]
Eng, Charis [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Cleveland Clin Fdn, Genom Med Inst, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Lerner Res Inst, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Cleveland Clin, Lerner Coll Med, Dept Mol Med, Cleveland, OH 44195 USA
[4] Cleveland Clin Fdn, Taussig Canc Inst, Cleveland, OH 44195 USA
[5] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
[6] Case Western Reserve Univ, Sch Med, CASE Comprehens Canc Ctr, Cleveland, OH 44106 USA
关键词
D O I
10.1016/j.ajhg.2008.07.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 3 75 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.
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收藏
页码:261 / 268
页数:8
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