Overexpression of p16INK4A as a specific marker for dysplastic and neoplastic epithelial cells of the cervix uteri
Гиперэкспрессия p16INK4A как специфический маркер диспластических и неопластических эпителиальных клеток шейки матки
2001-01-01
SCID: 54.1/6933snym
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cervical cancercervical intraepithelial neoplasiahigh-risk human papillomavirusimmunocytochemical detectionp16INK4A overexpression
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Abstract (AI)
Cytological screening for cervical cancer or its precursors using Papanicolaou's smear test (Pap test) has been highly efficient to reduce the morbidity and mortality of cervical cancer. However, evaluation of the Pap test relies on subjective diagnostic parameters and is affected by a high rate of false-positive and false-negative results. More objective diagnostic parameters to identify truly dysplastic or neoplastic cells in cervical smears as well as in cervical biopsy samples would therefore avoid insecurity for many patients and the high screening costs associated with repeated testing. Cervical dysplasia is induced by persistent infections through high-risk types of human papillomaviruses (HPVs). Outgrowth of dysplastic lesions is triggered by increasing expression of two viral oncogenes, E6 and E7, which both interact with various cell cycle-regulating proteins. Among these is the retinoblastoma gene product pRB, which is inactivated by E7. pRB inhibits transcription of the cyclin-dependent kinase inhibitor gene p16(INK4a). Increasing expression of the viral oncogenes in dysplastic cervical cells might thus be reflected by increased expression of p16(INK4a). In line with this hypothesis, we observed marked overexpression of p16(INK4a) in all cervical intraepithelial neoplasm (CIN) I lesions (n = 47) except those associated with low-risk HPV types (n = 7), all CIN II lesions (n = 32), all CIN III lesions (n = 60) and 58 of 60 invasive cervical cancers. In contrast, no detectable expression of p16(INK4a) was observed in normal cervical epithelium (n = 42), inflammatory lesions (n = 48) and low-grade cervical lesions (CIN I) associated with low-risk HPV types (n = 7). Dysplastic cells could also be identified in cervical smears using a specific p16(INK4a) monoclonal antibody. These data demonstrate that p16(INK4a) is a specific biomarker to identify dysplastic cervical epithelia in sections of cervical biopsy samples or cervical smears.
Key Findings
1
A monoclonal p16INK4A antibody enabled identification of dysplastic cells in cervical smears.
2
No detectable p16INK4A expression was observed in normal cervical epithelium, inflammatory lesions, or low-risk HPV-associated CIN I lesions.
3
p16INK4A may provide a more objective diagnostic parameter than conventional Pap-test assessment, which is subject to false-positive and false-negative results.
4
p16INK4A overexpression provides a specific biomarker for detecting dysplastic and neoplastic cervical epithelium in biopsy sections and cervical smears.
5
p16INK4A was markedly overexpressed in all high-risk HPV-associated CIN I lesions, all CIN II and CIN III lesions, and 58 of 60 invasive cervical cancers.
Research Object
Dysplastic, neoplastic, and normal cervical epithelial cells and lesions, including cervical intraepithelial neoplasia and invasive cervical cancer
Research Subject
p16INK4A expression as a specific marker for identifying dysplastic and neoplastic cervical epithelial cells
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2001-01-01
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