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DOI 10.1016/j.yexmp.2015.01.007

Медицинская библиотека · Experimental and molecular pathology · 2015

HPV DNA genotyping and methylation of gene p16 INK4A in cervical LSIL.

Silveira Filomena Aste, Almeida Gutemberg, Furtado Yara, Silva Kátia S, Maldonado Paula, Cavalcanti Silvia, Carvalho Maria da Gloria da Costa

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

DNA methylation is the most important epigenetic change involved in the control of gene expression in human cells. Methylation of the p16(INK4a) gene occurs early in the development of cervical cancer. Low-grade squamous intraepithelial lesions (LSILs) are prevalent, and their behavior is variable.

OBJECTIVE

To identify the HPV DNA type, detect the methylation status of the p16(INK4A) gene, and analyze their association with the cytological evolution of LSIL over a period of two years.

METHODS

We conducted a cohort study with 40 participants. Cervical scrapings were collected for cytological and molecular analysis. HPV DNA detection and typing were performed by means of polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP). Methylation-specific PCR was performed to detect methylation.

RESULTS

HPV DNA was detected in 87% of the cases, and type 16 was the most frequent type. Methylation was detected in 11% of the cases and did not exhibit a significant correlation with the HPV type. Unfavorable cytological evolution exhibited a significant association with the presence of methylation.

CONCLUSION

HPV 16 was the most frequently detected type of HPV in LSIL. Methylation of the p16(INK4A) gene was infrequent and occurred independent of the presence of HPV DNA. Methylation of the p16(INK4a) gene exhibited a significant correlation with persistence/progression of LSIL.

Для цитирования: Silveira Filomena Aste, Almeida Gutemberg, Furtado Yara, Silva Kátia S, Maldonado Paula, Cavalcanti Silvia, Carvalho Maria da Gloria da Costa. HPV DNA genotyping and methylation of gene p16 INK4A in cervical LSIL.. Experimental and molecular pathology. 2015. DOI: 10.1016/j.yexmp.2015.01.007.

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