Section on Endocrinology and Genetics and Pediatric Endocrinology Training Program, both at Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1103, USA.
Clin Endocrinol (Oxf). 2012 Aug;77(2):195-9. doi: 10.1111/j.1365-2265.2012.04366.x.
Genetic aberrations in various components of cAMP signalling pathway predispose to endocrine tumours. Mutations in the phosphodiesterases (PDEs) are involved in the predisposition to adrenocortical neoplastic conditions.
To screen for genetic variations in PDE8B among patients with different types of adrenocortical tumours.
This is a case-control study followed by functional analyses. Two hundred and sixteen unrelated patients with different types of adrenocortical tumours and 192 healthy control individuals participated in the study.
Bidirectional Sanger sequencing, in vitro cell line transfection and in silico modelling are used in this study.
Nine different PDE8B sequence changes, six novel and three previously reported, were identified in our patients and controls. Two of the variations, seen only in the patient group, showed significant potential to impair protein function, both in vitro and in silico.
PDE8B is another PDE gene in which variations may contribute to predisposition of adrenocortical tumours.
细胞环磷酸腺苷信号通路的各种成分的遗传异常使内分泌肿瘤易于发生。磷酸二酯酶(PDEs)的突变与肾上腺皮质肿瘤的易感性有关。
在不同类型的肾上腺皮质肿瘤患者中筛选 PDE8B 的遗传变异。
这是一项病例对照研究,随后进行功能分析。216 名患有不同类型肾上腺皮质肿瘤的无血缘关系的患者和 192 名健康对照者参与了这项研究。
本研究采用双向 Sanger 测序、体外细胞系转染和计算机模拟。
在我们的患者和对照组中发现了 9 种不同的 PDE8B 序列变化,其中 6 种是新的,3 种是以前报道过的。仅在患者组中发现的两种变异在体外和计算机模拟中均显示出显著的潜在蛋白功能损伤。
PDE8B 是另一个可能导致肾上腺皮质肿瘤易感性的 PDE 基因。