Lee Ji-Young, Kim Su Yeon, Mo Eun-Yeong, Kim Eun-Sook, Han Je-Ho, Maeng Lee-So, Lee An-Hee, Eun Jung Woo, Nam Suk Woo, Moon Sung-Dae
Division of Endocrinology and Metabolism, Department of Internal Medicine, Incheon St. Mary's Hospital, The Catholic University of Korea, Bupyeong-gu, Incheon 403-720, Republic of Korea.
Department of Hospital Pathology, Incheon St. Mary's Hospital, The Catholic University of Korea, Bupyeong-gu, Incheon 403-720, Republic of Korea.
Int J Oncol. 2014 Aug;45(2):641-50. doi: 10.3892/ijo.2014.2477. Epub 2014 May 29.
Mutations of the HRPT2 gene, which are responsible for hyperparathyroidism-jaw tumor (HPT-JT) syndrome, have been implicated in the development of a high proportion of parathyroid carcinomas. The aim of this study was to investigate differences in expression of the most important genes connected with parathyroid carcinoma between HPT-JT syndrome due to an HRPT2 splicing mutation, normal parathyroid tissue and sporadic parathyroid adenoma. Total RNAs were extracted from parathyroid carcinoma in HPT-JT syndrome harbouring HRPT2 splicing mutation or sporadic parathyroid adenoma and normal parathyroid gland, and subjected to Illumina DASL-based gene expression assay. Unsupervised hierarchical clustering analysis was used to compare gene expression in HPT-JT syndrome, sporadic parathyroid adenoma and normal parathyroid glands. We identified differentially regulated genes in HPT-JT syndrome and sporadic parathyroid adenoma relative to normal parathyroid glands using a combination of Welch's t-test and fold-change analysis. Quantitative PCR, RT-PCR and IHC were used for validation. Sixteen genes differentially regulated in the parathyroid carcinoma were associated with signal pathways, MAPK, regulation of actin cytoskeleton, prostate cancer and apoptosis. FGFR1 expression was confirmed to be significantly upregulated by validation experiments. Our gene expression profiling experiments suggest that upregulated FGFR1 expression appears to be associated with parathyroid carcinoma in HPT-JT syndrome due to an HRPT2 splicing mutation.
导致甲状旁腺功能亢进-颌骨肿瘤(HPT-JT)综合征的HRPT2基因突变与高比例的甲状旁腺癌发生有关。本研究的目的是调查因HRPT2剪接突变导致的HPT-JT综合征、正常甲状旁腺组织和散发性甲状旁腺腺瘤之间与甲状旁腺癌相关的最重要基因的表达差异。从携带HRPT2剪接突变的HPT-JT综合征甲状旁腺癌或散发性甲状旁腺腺瘤以及正常甲状旁腺中提取总RNA,并进行基于Illumina DASL的基因表达分析。采用无监督层次聚类分析比较HPT-JT综合征、散发性甲状旁腺腺瘤和正常甲状旁腺中的基因表达。我们结合Welch t检验和倍数变化分析,确定了HPT-JT综合征和散发性甲状旁腺腺瘤相对于正常甲状旁腺中差异调节的基因。采用定量PCR、RT-PCR和免疫组化进行验证。在甲状旁腺癌中差异调节的16个基因与信号通路、MAPK、肌动蛋白细胞骨架调节、前列腺癌和细胞凋亡有关。验证实验证实FGFR1表达显著上调。我们的基因表达谱实验表明,由于HRPT2剪接突变,FGFR1表达上调似乎与HPT-JT综合征中的甲状旁腺癌有关。