Expression of P57(kip2) and cyslinE proteins in human pancreatic cancer.
- Author:
Hui YUE
1
;
Jieping YU
;
Xin ZHAO
;
Fulin SONG
;
Xinli FENG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Cyclin E; analysis; Cyclin-Dependent Kinase Inhibitor p57; Female; Humans; Immunohistochemistry; Male; Middle Aged; Nuclear Proteins; analysis; Pancreatic Neoplasms; chemistry; pathology
- From: Chinese Medical Journal 2003;116(6):944-946
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo investigate the effects of p57(kip2) and cyclinE proteins on the genesis and progression of human pancreatic cancer.
METHODSThe expression of p57(kip2) and cyclinE proteins in tumor tissues and adjacent tissues of pancreatic cancer in 32 patients was detected by SP immunohistochemical technique.
RESULTSThe p57(kip2) protein positive-expression rate in tumor tissues of pancreatic cancer was 46.9%, which was lower than that in adjacent pancreatic tissue (P < 0.05). The p57(kip2) protein positive-expression correlated significantly with tumor cell differentiation (P < 0.05) and did not correlate significantly with lymph node metastasis (P > 0.05). The cyclinE positive-expression rate in tumor tissues was 68.8%, which was higher than that in adjacent pancreatic tissues (P < 0.05). The cyclinE positive-expression also correlated significantly with tumor cell differentiation and lymph node metastasis (P < 0.05). The cyclinE protein positive-expression rate in the tumor tissues of the p57(kip2) protein positive-expression group was lower than that in the p57(kip2) protein negative-expression group, and there were no significant correlation between the two groups (r = -0.112, P > 0.05).
CONCLUSIONDecreased expression of the p57(kip2) protein and/or over-expression of the cyclinE protein may play an important role in the genesis and progression of human pancreatic cancer.
