PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) - A NEW MARKER TO STUDY HUMAN COLONIC CELL-PROLIFERATION

被引:154
|
作者
KUBBEN, FJGM
PEETERSHAESEVOETS, A
ENGELS, LGJB
BAETEN, CGMI
SCHUTTE, B
ARENDS, JW
STOCKBRUGGER, RW
BLIJHAM, GH
机构
[1] ACAD HOSP MAASTRICHT,DEPT GEN SURG,6202 AZ MAASTRICHT,NETHERLANDS
[2] ACAD HOSP MAASTRICHT,DEPT INTERNAL MED,DIV GASTROENTEROL,6202 AZ MAASTRICHT,NETHERLANDS
[3] ACAD HOSP MAASTRICHT,DEPT PATHOL,6202 AZ MAASTRICHT,NETHERLANDS
[4] MAASLAND HOSP,DEPT GASTROENTEROL,SITTARD,NETHERLANDS
[5] ACAD HOSP UTRECHT,DEPT INTERNAL MED,DIV HAEMATOONCOL,UTRECHT,NETHERLANDS
[6] UNIV LIMBURG,DEPT MOLEC CELL BIOL,6200 MD MAASTRICHT,NETHERLANDS
关键词
D O I
10.1136/gut.35.4.530
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Immunohistochemistry of the S phase related proliferating cell nuclear antigen (PCNA) was studied as an alternative to ex-vivo bromodeoxyuridine (BrdU) immunohistochemistry for assessment of human colonic cell proliferation. From 16 subjects without colonic disease biopsy specimens were collected from five different sites along the colorectum and processed for BrdU and PCNA immunohistochemistry. The mean proliferation index of PCNA was significantly higher at 133% of the value obtained with BrdU. There was, however, a good correlation between the results from both techniques (r=0.6275; p<0.05). Decrease in proliferation index along the colorectum was seen with both staining methods but was clearer with PCNA immunohistochemistry (caecum/ascending colon v rectum: 12.0 v 7.2; p<0.004). The total number of crypt cells also decreased from proximal to distal (134 to 128; p<0.06) but at no site correlated significantly with the proliferation index. It is concluded that in clinical cell kinetic studies staining for PCNA may serve as an attractive alternative to the BrdU incorporation assay.
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收藏
页码:530 / 535
页数:6
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