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基因表达和甲基化谱显示 POMC 参与原发性甲状旁腺功能亢进症。

Gene expression and methylation profiles show the involvement of POMC in primary hyperparathyroidsm.

机构信息

Department of Pathology, Xiangya Hospital, Central South University, Changsha, 410000, Hunan, China.

Department of Pathology, School of Basic Medical Science, Central South University, Changsha, 410000, Hunan, China.

出版信息

J Transl Med. 2022 Aug 16;20(1):368. doi: 10.1186/s12967-022-03568-4.

Abstract

Primary hyperparathyroidism (PHPT) is mainly caused by parathyroid adenoma, which produces excess parathyroid hormones. Its pathogenic mechanisms have not yet been fully understood. To investigate the mechanism in the pathogenesis of PHPT, the transcriptome and genome-wide DNA methylation profiles of parathyroid adenoma were analyzed. The candidate genes that may be involved in the PHPT were verified via qRT-PCR, immunohistochemistry, western blot, and methylation-specific PCR. A total of 1650 differentially expressed genes and 2373 differentially methylated regions were identified. After the integration of its transcriptome and DNA methylation data, IL6, SYP, GNA01, and pro-opiomelanocortin (POMC) were the candidate genes that demonstrated a similar pattern between their mRNA expression and DNA methylation status. Of the 4 candidate genes, POMC, a pro-peptide which is processed to a range of bioactive peptide products like ACTH, was further confirmed to be expressed at low levels at both the mRNA and protein levels, which may be due to POMC promoter hypermethylation. Hypermethylation of the POMC promoter may contribute to its low expression, which may be involved in the pathogenesis of PHPT.

摘要

原发性甲状旁腺功能亢进症(PHPT)主要由甲状旁腺腺瘤引起,其产生过多的甲状旁腺激素。其发病机制尚未完全阐明。为了研究 PHPT 发病机制中的机制,分析了甲状旁腺腺瘤的转录组和全基因组 DNA 甲基化谱。通过 qRT-PCR、免疫组织化学、western blot 和甲基化特异性 PCR 验证了可能参与 PHPT 的候选基因。鉴定出 1650 个差异表达基因和 2373 个差异甲基化区域。在其转录组和 DNA 甲基化数据的整合后,IL6、SYP、GNA01 和 pro-opiomelanocortin(POMC)是 mRNA 表达和 DNA 甲基化状态相似的候选基因。在 4 个候选基因中,POMC 是一种前肽,可加工成一系列生物活性肽产物,如 ACTH,其在 mRNA 和蛋白质水平上的表达均较低,这可能是由于 POMC 启动子过度甲基化所致。POMC 启动子的高甲基化可能导致其低表达,这可能与 PHPT 的发病机制有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a12e/9382844/f82bdbca323e/12967_2022_3568_Fig1a_HTML.jpg

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