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Updated: Apr 18, 2026

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Published on: September 7, 2017
TIMP-2 gene methylation in cervical precursor and invasive lesions
Yara Furtado1, Gutemberg Almeida2, Filomena Aste Silveira2
1Universidade Federal do Estado do Rio de Janeiro (UNIRIO), Brazil; Postgraduate Program in Surgical Sciences, Universidade Federal do Rio de Janeiro - UFRJ, Brazil; Institute of Gynecology, Universidade Federal do Rio de Janeiro (UFRJ), Brazil.
Objective:
To analyze the presence of HPV-DNA and TIMP-2 gene methylation in cervical precursor and invasive lesions, as well as to study the associations among the latter, the presence of HPV-DNA, and the clinical evolution of such lesions.
Methods:
Cross-sectional study that includes 49 biopsy or brush smear samples from women with a normal cervix, LSIL, HSIL, microinvasive carcinoma and invasive carcinoma. The presence of HPV-DNA and specific methylation was analyzed using PCR. Thirty-eight biopsy samples for HSIL, microinvasive carcinoma and frank invasive carcinoma as well as 11 brush smear samples for LSIL and normal cervices were analyzed.
Results:
TIMP-2 gene methylation was detected in 86.8% (33/38) of the samples from the group with lesions and 50% (4/8) of the normal samples (p=0.03). HPV-DNA was detected in 81.6% (31/38) of the samples from the group with lesions and 25% (2/8) of the normal samples (p=0.003). HPV-DNA was more frequent in the methylated samples (50%), and the group with methylation had a higher risk of unfavorable evolution than the group without methylation; however, such observations were not statistically significant (p=0.19).
Conclusion:
TIMP-2 gene methylation and the presence of HPV-DNA were characteristic of the group with cervical lesions. Methylation was not associated with the presence of HPV-DNA or an unfavorable clinical evolution.
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