Gene methylation of CADM1 and MAL identified as a biomarker of high grade anal intraepithelial neoplasia

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作者
Samuel Phillips
Kahli Cassells
Suzanne M. Garland
Dorothy A. Machalek
Jennifer M. Roberts
David J. Templeton
Fengyi Jin
I. Mary Poynten
Richard J. Hillman
Andrew E. Grulich
Gerald L. Murray
Sepehr N. Tabrizi
Monica Molano
Alyssa M. Cornall
机构
[1] University of Melbourne,Department of Obstetrics and Gynecology
[2] The Royal Women’s Hospital,Centre Women’s Infectious Diseases Research
[3] Murdoch Children’s Research Institute,HIV Epidemiology and Prevention Program, The Kirby Institute
[4] University of New South Wales,Department of Sexual Health Medicine
[5] Douglass Hanly Moir Pathology,Discipline of Medicine, Central Clinical School, Faculty of Medicine and Health
[6] Sydney Local Health District,Dysplasia and Anal Cancer Services
[7] The University of Sydney,undefined
[8] St Vincent’s Hospital,undefined
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Human papillomavirus (HPV) is detected in up to 96% of anal squamous cell cancers, where screening programs needed. However, the best methodology is still undetermined. Host DNA methylation markers CADM1, MAL and miR124 have been identified in cervical disease, but not anal disease. Anal swabs varying by disease grade were assessed for DNA methylation of CADM1, MAL and miR124-2. Each marker was compared across disease grades, stratified by HPV and HIV status. Receiver operating characteristic curves identified the predictive value of significant gene candidates. CADM1 methylation was significantly higher in high-grade squamous intraepithelial lesions (HSIL) compared with low-grade (LSIL) (p = 0.005) or normal (p < 0.001) samples with 67.2% correctly identified as HSIL. MAL methylation was significantly (p = 0.002) increased in HSIL compared with LSIL in HIV positive participants with 79.8% correctly indicated as HSIL. Gene miR124-2, showed no difference between disease grades. Biomarkers with established diagnostic value in cervical disease have limited utility in the prediction of anal disease, with CADM1 identified as a marker with screening potential in a gay and bisexual men (GBM) population and MAL in HIV positive GBM population. New markers specific to the anal mucosa are required to improve triage of high-risk individuals.
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