Department of Pediatric Hematology-Oncology, Dana Farber Cancer Institute and Children's Hospital, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):314-8. doi: 10.1073/pnas.1009199108. Epub 2010 Dec 20.
Carney-Stratakis syndrome, an inherited condition predisposing affected individuals to gastrointestinal stromal tumor (GIST) and paraganglioma, is caused by germline mutations in succinate dehydrogenase (SDH) subunits B, C, or D, leading to dysfunction of complex II of the electron transport chain. We evaluated the role of defective cellular respiration in sporadic GIST lacking mutations in KIT or PDGFRA (WT). Thirty-four patients with WT GIST without a personal or family history of paraganglioma were tested for SDH germline mutations. WT GISTs lacking demonstrable SDH genetic inactivation were evaluated for SDHB expression by immunohistochemistry and Western blotting and for complex II activity. For comparison, SDHB expression was also determined in KIT mutant and neurofibromatosis-1-associated GIST, and complex II activity was also measured in SDH-deficient paraganglioma and KIT mutant GIST; 4 of 34 patients (12%) with WT GIST without a personal or family history of paraganglioma had germline mutations in SDHB or SDHC. WT GISTs lacking somatic mutations or deletions in SDH subunits had either complete loss of or substantial reduction in SDHB protein expression, whereas most KIT mutant GISTs had strong SDHB expression. Complex II activity was substantially decreased in WT GISTs. WT GISTs, particularly those in younger patients, have defects in SDH mitochondrial complex II, and in a subset of these patients, GIST seems to arise from germline-inactivating SDH mutations. Testing for germline mutations in SDH is recommended in patients with WT GIST. These findings highlight a potential central role of SDH dysregulation in WT GIST oncogenesis.
卡尼-斯特拉塔斯基综合征是一种遗传性疾病,使受影响的个体易患胃肠道间质瘤(GIST)和副神经节瘤,是由琥珀酸脱氢酶(SDH)亚基 B、C 或 D 的种系突变引起的,导致电子传递链复合物 II 的功能障碍。我们评估了缺乏 KIT 或 PDGFRA 突变的散发性 GIST 中细胞呼吸缺陷的作用(WT)。对 34 名无副神经节瘤个人或家族史的 WT GIST 患者进行 SDH 种系突变检测。对缺乏可检测的 SDH 遗传失活的 WT GIST 进行 SDHB 表达的免疫组织化学和 Western 印迹分析,并评估复合物 II 活性。为了比较,还确定了 KIT 突变和神经纤维瘤病 1 相关 GIST 中的 SDHB 表达,并测量了 SDH 缺陷性副神经节瘤和 KIT 突变 GIST 中的复合物 II 活性;4 例(12%)无副神经节瘤个人或家族史的 WT GIST 患者存在 SDHB 或 SDHC 的种系突变。缺乏 SDH 亚基体细胞突变或缺失的 WT GIST 要么完全丧失或大量减少 SDHB 蛋白表达,而大多数 KIT 突变 GIST 具有强烈的 SDHB 表达。WT GIST 的复合物 II 活性显著降低。WT GIST,特别是年轻患者,存在 SDH 线粒体复合物 II 的缺陷,在这些患者中的一部分,GIST 似乎来自种系失活的 SDH 突变。建议对 WT GIST 患者进行 SDH 种系突变检测。这些发现强调了 SDH 失调在 WT GIST 发生中的潜在核心作用。