P16INK4a expression as a potential prognostic marker in cervical pre-neoplastic and neoplastic lesions

被引:29
作者
Queiroz, C
Silva, TC
Alves, VAF
Villa, LL
Costa, MC
Travassos, AG
Araújo, JB
Studart, E
Cheto, T
de Freitas, LAR
机构
[1] Univ Fed Bahia, Sch Med, Dept Gynecol & Obstet, BR-40210 Salvador, BA, Brazil
[2] Univ Fed Bahia, Sch Med, Dept Pathol, BR-40210 Salvador, BA, Brazil
[3] Fiocruz MS, Oswaldo Cruz Fdn, Goncalo Moniz Res Ctr, Salvador, BA, Brazil
[4] Univ Fed Sao Paulo, Adolfo Lutz Inst, Dept Pathol, Sao Paulo, Brazil
[5] Ludwig Inst Canc Res, Dept Virol, Sao Paulo, Brazil
关键词
cervical neoplasia; diagnostic marker; p16(INK4a); human papillomavirus; human immunodeficiency virus;
D O I
10.1016/j.prp.2005.08.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
An immunohistochemical analysis with monoclonal antibody p16(INK4), was performed in formalin-fixed, paraffin-embedded samples of 60 cases. The aim was to investigate in biopsies the expression of p16(INK4a) of normal uterine cervical tissue, pre-cancerous and cancerous lesions, and their relation with human papilloma virus (HPV) and HIV status. Three parameters were evaluated: percentage of p16(INK4a) positive cells, reaction intensity, and cell staining pattern. All of these parameters were statistically different when compared among different histological groups. However, logistic regression model showed that the reaction intensity was the best indicator of the expression of p16(INK4a). This expression increases from normal to invasive squamous carcinoma. Sixty-six percent of the patients with CIN grade 1 (CIN1) expressed p16(INK4a) (all these cases were infected with high risk HPV). Our study supports the hypothesis that p16(INK4a) expression in pre-cancerous lesions and cancers can be used to identify HPV-transformed cells. Of great interest for routine diagnostic use is the fact that immunohistochemical testing for p16(INK4a) seems to be capable of identifying HPV-positive cells and potentially recognizing those lesions with an increased risk of progression to high-grade lesions. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:77 / 83
页数:7
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