P16INK4a expression is a surrogate marker of HPV E7-mediated pRB catabolism and is a sensitive and specific marker of high-grade premalignant and malignant lesions in cervical tissue biopsies. The utility of P16INK4a as a diagnostic adjunct for cervical cytology however, remains relatively unexplored. The goal of this R21/R33 phased innovation and application proposal is to evaluate the expression of P16INK4a as a diagnostic adjunct in cases with low-grade cytologic abnormalities including ASC-US, ASC-H, LSIL, and AGC, to identify cases that are most likely to have underlying high-grade premalignant lesions on cervical biopsy, The specific aims of the R21 application are: 1) to validate the immunocytochemical method for the detection of P16INK4a in cervical cytology specimens; 2) to define quantitative criteria for scoring P16INK4a test results; 3) to develop a pilot series of """"""""gold standard"""""""" cytology specimens for P16INK4a analysis; and 4) to perform a preliminary evaluation of P16INK4a cytology test performance in """"""""gold standard"""""""" cytology cases.
The specific aims of the R33 proposal are: 1) to determine the correlation between the P16INK4a and high risk HPV detection with cytologic diagnoses in cases with normal cytology and in cases with ASC-US, ASC-H, LSIL, and AGC; 2) to determine the correlation between P16INK4a and high risk HPV detection in low grade cervical cytology specimens with the biopsy diagnosis of high-grade squamous or glandular lesions of the cervical squamous mucosa; 3) to determine the correlation between pl6lNK4a detection in low grade cervical cytology specimens with the histologic distribution of pl6lNK4a in concurrently collected cervical biopsies; and 4) to determine the optimal combination of cytology test procedures to maximize sensitivity and specificity for the detection of high-grade lesions on cervical biopsy. If successful, this study will provide a mechanism to identify patients that require aggressive clinical management and to defer the aggressive management of patients that will not benefit from further diagnostic evaluation.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants Phase II (R33)
Project #
4R33CA110519-02
Application #
7121745
Study Section
Special Emphasis Panel (ZCA1-SRRB-3 (M2))
Program Officer
Sorbara, Lynn R
Project Start
2004-07-06
Project End
2008-06-30
Budget Start
2005-09-21
Budget End
2006-06-30
Support Year
2
Fiscal Year
2005
Total Cost
$150,152
Indirect Cost
Name
University of Colorado Denver
Department
Pathology
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Samarawardana, Panduka; Singh, Meenakshi; Shroyer, Kenneth R (2011) Dual stain immunohistochemical localization of p16INK4A and ki-67: a synergistic approach to identify clinically significant cervical mucosal lesions. Appl Immunohistochem Mol Morphol 19:514-8
Samarawardana, Panduka; Dehn, Donna L; Singh, Meenakshi et al. (2010) p16(INK4a) is superior to high-risk human papillomavirus testing in cervical cytology for the prediction of underlying high-grade dysplasia. Cancer Cytopathol 118:146-56