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p16INK4A as a marker for cervical dyskaryosis: CIN and cGIN in cervical biopsies and ThinPrep™ smears
  1. N Murphy2,
  2. M Ring1,
  3. A G Killalea1,
  4. V Uhlmann1,
  5. M O’Donovan2,
  6. F Mulcahy4,
  7. M Turner3,
  8. E McGuinness3,
  9. M Griffin5,
  10. C Martin1,
  11. O Sheils2,
  12. J J O’Leary1
  1. 1Department of Pathology, Coombe Women’s Hospital, Dublin 8, Ireland
  2. 2Trinity College Dublin, Dublin 2, Ireland
  3. 3Department of Obstetrics and Gynaecology, The Coombe Women’s Hospital
  4. 4Department of Genitourinary Medicine, St James’s Hospital, Dublin, Ireland
  5. 5Department of Histopathology, St James Hospital
  1. Correspondence to:
 Ms N Murphy, Department of Pathology, Coombe Women’s Hospital, Dublin 8, Ireland; 
 ncmurphy{at}tcd.ie

Abstract

Aim: To examine the potential of p16INK4A as a biomarker for dysplastic squamous and glandular cells of the cervix in tissue sections and ThinPrep™ smears.

Methods: Immunocytochemical analysis of p16INK4A expression was performed on 22 normal cervical tissue samples, five cervical glandular intraepithelial neoplasia (cGIN), 38 cervical intraepithelial neoplasia 1 (CIN1), 33 CIN2, 46 CIN3, and 10 invasive cancer cases (eight squamous and two adenocarcinomas). All samples were formalin fixed and paraffin wax embedded, and immunohistochemical analysis was carried out using a mouse monoclonal anti-p16INK4A antibody after antigen unmasking. The staining intensity was assessed using a 0 to 3 scoring system. In addition, the expression status of p16INK4A was examined in 12 normal ThinPrep smears, one smear exhibiting cGIN, and a total of 20 smears exhibiting mild, moderate, and severe dyskaryosis. Human papillomavirus (HPV) detection was carried out using a modified SYBR green assay system. Fluorogenic polymerase chain reaction (PCR) and solution phase PCR were used for specific HPV typing.

Results: p16INK4A immunoreactivity was absent in all normal cervical tissues examined. Dysplastic squamous and glandular cells were positive for p16INK4A expression in all cases included in this study, except for one CIN3 case. p16INK4A expression was mainly nuclear in CIN1 cases, and both nuclear and cytoplasmic in CIN2, CIN3, cGIN, and invasive cases. All cases positive for HPV expressed the p16INK4A protein, although not all cases found positive for p16INK4A were HPV positive. In general, the p16INK4A staining intensity was lower in cases negative for HPV or those containing a low risk HPV type.

Conclusion: This pattern of overexpression demonstrates the potential use of p16INK4A as a diagnostic marker for cervical squamous and also glandular neoplastic lesions. In addition, the technique can be used to identify individual dyskaryotic cells in ThinPrep smears. Thus, p16INK4A is a useful marker of cervical dyskaryosis.

  • p16
  • dyskaryosis
  • marker
  • BSA, bovine serum albumin
  • cdk, cyclin dependent kinase
  • CIN, cervical intraepithelial neoplasia
  • HPV, human papillomavirus
  • Pap, Papanicolaou test
  • PBST, phosphate buffered saline/Tween 20
  • PCR, polymerase chain reaction
  • pRb, retinoblastoma protein
  • TBS, Tris buffered saline

https://doi.org/10.1136/jcp.56.1.56

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