期刊
DIAGNOSTIC CYTOPATHOLOGY
卷 36, 期 2, 页码 76-84出版社
WILEY
DOI: 10.1002/dc.20763
关键词
cervical cancer; cancer screening; flow cytometry; cancer markers; rare-event detection
资金
- NCI NIH HHS [1R21 CA 125370-01] Funding Source: Medline
The Pap test used for cervical cancer screening is subjective, labor-intensive, and has relatively low sensitivity and specificity for the detection of underlying clinically significant lesions. The objective of this study is to develop a biomarker/flow cytometry-based approach for cervical cancer screening. Immunofluorescence technology to quantify cervical cell expression of two biomarkers p16(INK4A) and Mcm5 was developed and evaluated by both microcopy and flow cytometry. The capability of using biomarker/flow cytometry approach to detect rare-event dysplastic cells in a large background of benign epithelial and inflammatory cells was evaluated. The results indicate that flow cytometry could detect 0.01% dysplastic cells in a background of normal cervical epithelial cells with the combination of the two biomarkers. Thirty-two clinical specimens were used to test the biomarker/flow cytometry-based approach and the results were compared with the liquid-based cervical cytology. The experiment yielded 100% sensitivity and 93% specificity with reference to the liquid-based cervical cytology. This study indicates the promise of using multi-color fluorescence flow cytometry for biomarker-based cervical cancer screening. This molecular-based, potentially high -throughput and automated method is expected to provide an alternative/auxiliary means of cervical cancer screening.
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