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Analysis of all subunits, SDHA, SDHB, SDHC, SDHD, of the succinate dehydrogenase complex in KIT/PDGFRA wild-type GIST

SDHA SDHB系统 SDHD公司 PDGFRA公司 主旨 癌症研究 生物 副神经节瘤 种系突变 突变 遗传学 琥珀酸脱氢酶 医学 病理 基因 线粒体 间质细胞
作者
Maria Abbondanza Pantaleo,Annalisa Astolfi,Milena Urbini,Margherita Nannini,Paola Paterini,Valentina Indio,Maristella Saponara,Serena Formica,Claudio Ceccarelli,Rita Casadio,Giulio Rossi,Federica Bertolini,Donatella Santini,Maria Giulia Pirini,Michelangelo Fiorentino,Umberto Basso,Guido Biasco
出处
期刊:European Journal of Human Genetics [Springer Nature]
卷期号:22 (1): 32-39 被引量:92
标识
DOI:10.1038/ejhg.2013.80
摘要

Mutations of genes encoding the subunits of the succinate dehydrogenase (SDH) complex were described in KIT/PDGFRA wild-type GIST separately in different reports. In this study, we simultaneously sequenced the genome of all subunits, SDHA, SDHB, SDHC, and SDHD in a larger series of KIT/PDGFRA wild-type GIST in order to evaluate the frequency of the mutations and explore their biological role. SDHA, SDHB, SDHC, and SDHD were sequenced on the available samples obtained from 34 KIT/PDGFRA wild-type GISTs. Of these, in 10 cases, both tumor and peripheral blood (PB) were available, in 19 cases only tumor, and in 5 cases only PB. Overall, 9 of the 34 patients with KIT/PDGFRA wild-type GIST carried mutations in one of the four subunits of the SDH complex (six patients in SDHA, two in SDHB, one in SDHC). WB and immunohistochemistry analysis showed that patients with KIT/PDGFRA wild-type GIST who harbored SDHA mutations exhibited a significant downregulation of both SDHA and SDHB protein expression, with respect to the other GIST lacking SDH mutations and to KIT/PDGFRA-mutated GIST. Clinically, four out of six patients with SDHA mutations presented with metastatic disease at diagnosis with a very slow, indolent course. Patients with KIT/PDGFRA wild-type GIST may harbor germline and/or de novo mutations of SDH complex with prevalence for mutations within SDHA, which is associated with a downregulation of SDHA and SDHB protein expression. The presence of germline mutations may suggest that these patients should be followed up for the risk of development of other cancers.
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