Literature DB >> 31325108

Methylation of the CDKN2A Gene Increases the Risk of Brain Arteriovenous Malformations.

Xiaosheng Chen1, Yuchun Liu1,2, Shengjun Zhou1,2, Sheng Nie1,2, Zhiqin Lin1,2, Chenhui Zhou1,2, Jie Sun3,4, Xiang Gao5,6, Yi Huang7,8.   

Abstract

Brain arteriovenous malformations (BAVMs) and intracranial aneurysms (IAs) are the results of a combination of genetic and environmental factors. Epigenetic factors also play an important role in the pathogenesis of these disorders. The aim of this study was to determine the effect of DNA methylation at the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene on the risk of BAVMs and IAs. A total of 70 intracranial vascular malformation patients (22 patients with BAVMs and 48 patients with IAs) and 26 patients with cerebral trauma (used as controls) were included in this study. DNA methylation levels of eight cytosine-phosphate-guanine (CpG) dinucleotides present in the CDKN2A gene were measured using bisulfite pyrosequencing technology. Significant differences in methylation at CpG1 (p = 0.005), CpG5 (p = 0.011), and CpG8 (p = 0.017) were observed between BAVM patients and controls. CDKN2A methylation levels in BAVM patients were much higher than those in IA patients (CpG5: p = 0.004; CpG8: p = 0.010). Significant differences were observed between female IA patients and female BAVM patients (CpG5: p = 0.006; CpG8: p = 0.005; mean: p = 0.015). Receiver operating characteristic (ROC) curve analysis showed that the CDKN2A gene methylation trended toward a diagnostic indicator in BAVM patients (area under curve = 0.711, p = 0.013). In conclusion, our study demonstrated that the CDKN2A gene methylation levels are significantly correlated with the occurrence of BAVMs, and thus, have potential for use in the early diagnosis of BAVMs. Future research on the pathogenesis of BAVMs should focus on the role of genetic factors in aberrant venous development. The association of the CDKN2A gene with venous development also deserves further study.

Entities:  

Keywords:  Brain arteriovenous malformations; Cyclin-dependent kinase inhibitor 2A; DNA methylation; Epigenetics; Intracranial aneurysms

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Substances:

Year:  2019        PMID: 31325108     DOI: 10.1007/s12031-019-01360-6

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  4 in total

1.  Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis.

Authors:  Concetta Scimone; Francesca Granata; Marcello Longo; Enricomaria Mormina; Cristina Turiaco; Antonio A Caragliano; Luigi Donato; Antonina Sidoti; Rosalia D'Angelo
Journal:  Int J Mol Sci       Date:  2020-06-17       Impact factor: 5.923

2.  DNA methylation signatures on vascular differentiation genes are aberrant in vessels of human cerebral arteriovenous malformation nidus.

Authors:  Jaya Mary Thomas; Dhakshmi Sasankan; Mathew Abraham; Sumi Surendran; Chandrasekharan C Kartha; Arumugam Rajavelu
Journal:  Clin Epigenetics       Date:  2022-10-13       Impact factor: 7.259

Review 3.  Review of treatment and therapeutic targets in brain arteriovenous malformation.

Authors:  Peipei Pan; Shantel Weinsheimer; Daniel Cooke; Ethan Winkler; Adib Abla; Helen Kim; Hua Su
Journal:  J Cereb Blood Flow Metab       Date:  2021-06-23       Impact factor: 6.960

4.  Wilms' tumour 1-associating protein inhibits endothelial cell angiogenesis by m6A-dependent epigenetic silencing of desmoplakin in brain arteriovenous malformation.

Authors:  Lin-Jian Wang; Yimeng Xue; Hao Li; Ran Huo; Zihan Yan; Jie Wang; Hongyuan Xu; Jia Wang; Yong Cao; Ji-Zong Zhao
Journal:  J Cell Mol Med       Date:  2020-04-13       Impact factor: 5.310

  4 in total

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