4.4 Article

p16INK4 expression in precursor lesions of squamous cell cervical cancer related to the presence of HPV-DNA

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Publisher

ASSOC BRAS DIVULG CIENTIFICA
DOI: 10.1590/S0100-879X2008000700006

Keywords

p16(INK4); cervical cancer; human papillomavirus; immunohistochemistry

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The purpose of the present study was to identify the expression of p16(INK4) in cervical cancer precursor lesions by immunohistochemistry and to correlate it with lesion grade and presence of human papillomavirus (HPV) infection. Cervical specimens from 144 women seen consecutively at the gynecology outpatient clinic of our institution from December 2003 to May 2005 were analyzed by cytopathology, histopathology, polymerase chain reaction for HPV-DNA, and p16(INK4) immunostaining. Histologically normal biopsies, HPV-DNA negative by polymerase chain reaction, were used as control. HPV-DNA prevalence, including the control group, was 68.1% and the prevalence of p16(INK4) expression was 55.0%. The percentage of cells stained by p16(INK4) ranged from 10 to 100%, both in the group consisting of cervical intraepithelial neoplasia (CIN)1/HPV specimens and in the group of CIN2/CIN3 specimens with P value of 0.0001. p16(INK4) expression was 48.3% in the CIN1/HPV group, as opposed to 94.3% in the CIN2/CIN3 group (P = 0.001), showing a statistically significant difference between the two groups. The quantitative method used here is simple and less subjective than the different semiquantitative methods described in the literature. In view of the different definitions of a p16(INK4)-positive case, it is almost impossible to compare the findings reported by different investigators. This study confirms the association between p16(INK4) and CIN2 and CIN3 lesions. Moreover, it shows that some low grade lesions expressed high levels of this protein. This may indicate that such low grade lesions may be predisposed to progress to high grade lesions. This means that p16(INK4) may be a strong marker for neoplastic lesions induced by HPV and not just an infection marker.

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