PAN CYCLE EXPRESSION OF PROLIFERATING CELL NUCLEAR ANTIGEN IN HUMAN COLORECTAL-CANCER AND ITS PROLIFERATIVE CORRELATIONS

Citation
Rm. Sawtell et al., PAN CYCLE EXPRESSION OF PROLIFERATING CELL NUCLEAR ANTIGEN IN HUMAN COLORECTAL-CANCER AND ITS PROLIFERATIVE CORRELATIONS, Cytometry, 22(3), 1995, pp. 190-199
Citations number
29
Categorie Soggetti
Cell Biology","Biochemical Research Methods
Journal title
ISSN journal
01964763
Volume
22
Issue
3
Year of publication
1995
Pages
190 - 199
Database
ISI
SICI code
0196-4763(1995)22:3<190:PCEOPC>2.0.ZU;2-T
Abstract
Proliferating cell nuclear antigen (PCNA) is a key cell cycle regulato ry protein of known structure and function that also has an important role in DNA repair. Its use as a marker of proliferation can be assess ed directly using a thymidine analogue in suitably labelled pathologic al material, Following optimisation studies, a quantitative and cell c ycle phase-specific analysis of PCNA expression in fresh biopsies from 50 colorectal tumours (Series A) was undertaken using dual parameter flow cytometry (FCM), For comparison, quantitative histometric studies of PCNA expression were undertaken on 50 archival bromodeoxyuridine ( BrdUrd) labelled colorectal tumours (Series B), In FCM assays, PCNA-sp ecific fluorescence was displayed throughout the cell cycle in both ce lls and nuclei under all preparation conditions, but to a very variabl e extent. The mean PCNA labelling index ranged from 38.7% to 53.0% acc ording to the method of cell extraction used, In the 27 diploid tumour s in Series A, the median PCNA LI in G0/G1 was 71.5% (range 27.0-90.6% ), in S it was 10.5% (3.3-29.5%), and in G2/M it was 17.4% (5.7-43.5%) . In the histometric studies of Series B tumours, the mean [S.D.] PCNA labelling index (LI) was 38.8 [9.8]%, compared with the BrdUrd (histo metric) LI of 21.1 [9.0]%, The BrdUrd LI measured by FCM was 12.4 [6.5 ]%, PCNA-PC10 is expressed throughout the cell cycle in human colorect al tumour biopsies, which is in keeping with the range of DNA repair, synthesis, and regulatory functions that it is now recognised to perfo rm throughout the cell cycle. (C) 1995 Wiley-Liss, Inc.