The goal of this project is to apply multidimensional slit-scan technology to the examination and analysis of exfoliated bladder epithelium for the detection, diagnosis, and monitoring of cancer of the urinary bladder and its precursors. Static cell slit-scan cytofluorometer studies have been performed on bladder irrigation specimens representing a variety of cellular disorders of the bladder mucosa associated with and including invasive transitional cell carcinoma. Included in this database are normal specimens, specimens from low-grade papillary transitional cell carcinoma, and high-grade invasive cancer. Static cell analyses have suggested that correct identification of abnormal specimens from the bladder can be achieved utilizing the slit-scan technique with minimal modification of existing software. Abnormal cells derived from transitional cell carcinoma are delineated from normal cells by the feature nuclear fluorescence. Atypical cells of transitional type fall in an area between the normal and clearly abnormal cell populations. Other studies are directed at identifying potential causes of false alarms and developing a protocol for staining and fixing bladder irrigation specimens. One hundred eleven specimens have been analyzed in a preliminary clinical study on a multidimensional slit-scan flow system. These included 84 specimens representing a spectrum of abnormality present in the human bladder. The system false negative rate was 4.7% and the false positive rate was 17%. Current efforts are directed toward expanding this preliminary flow database and exploring the utility of other features available from multidimensional slit-scan analysis. (3)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA033148-06
Application #
3171112
Study Section
(SSS)
Project Start
1982-08-01
Project End
1988-06-30
Budget Start
1987-07-01
Budget End
1988-06-30
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Rochester
Department
Type
School of Medicine & Dentistry
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Wright, Kate O; Messing, Edward M; Reeder, Jay E (2004) DBCCR1 mediates death in cultured bladder tumor cells. Oncogene 23:82-90
Borhan, Ali; Reeder, Jay E; O'Connell, Mary J et al. (2003) Grade progression and regression in recurrent urothelial cancer. J Urol 169:2106-9
Wright, Kate O; Messing, Edward M; Reeder, Jay E (2002) Increased expression of the acid sphingomyelinase-like protein ASML3a in bladder tumors. J Urol 168:2645-9
Jung, I; Reeder, J E; Cox, C et al. (1999) Chromosome 9 monosomy by fluorescence in situ hybridization of bladder irrigation specimens is predictive of tumor recurrence. J Urol 162:1900-3
Reeder, J E; O'Connell, M J; Yang, Z et al. (1998) DNA cytometry and chromosome 9 aberrations by fluorescence in situ hybridization of irrigation specimens from bladder cancer patients. Urology 51:58-61
Reeder, J E; Cox, C; Wheeless, L L et al. (1997) Variability of DNA analysis by image cytometry. Bladder Tumor Marker Network. Cytometry 28:176-80
Reeder, J E; Morreale, J F; O'Connell, M J et al. (1997) Loss of the CDKN2A/p16 locus detected in bladder irrigation specimens by fluorescence in situ hybridization. J Urol 158:1717-21
Wheeless, L L; Reeder, J E; Han, R et al. (1994) Bladder irrigation specimens assayed by fluorescence in situ hybridization to interphase nuclei. Cytometry 17:319-26
Iwamura, M; Ishibe, M; Sluss, P M et al. (1993) Characterization of insulin-like growth factor I binding sites in human bladder cancer cell lines. Urol Res 21:27-32
Wheeless, L L; Coon, J S; Cox, C et al. (1991) Precision of DNA flow cytometry in inter-institutional analyses. Cytometry 12:405-12

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