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Loss of p27Kip1 expression is a strong independent prognostic factor of reduced survival in N0 gastric carcinomas

✍ Scribed by Alessandro Sgambato; Mario Migaldi; Piero Leocata; Luca Ventura; Mario Criscuolo; Carlo Di Giacomo; Giovanni Capelli; Achille Cittadini; Carmela De Gaetani


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
271 KB
Volume
89
Category
Article
ISSN
0008-543X

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✦ Synopsis


BACKGROUND. p27 Kip1 is a cyclin-dependent kinase inhibitor and is a potential tumor suppressor gene. Reduced expression of p27 Kip1 is a powerful negative prognostic marker in primary lung, breast, colon, bladder, and prostate carcinomas. In the current study, the prognostic value of p27 Kip1 in gastric cancer was evaluated and compared with other histopathologic parameters and p53 expression.

METHODS. p27 Kip1 and p53 protein expression were determined by immunohistochemistry in 96 gastric carcinomas. The tumors were from a low incidence population and were selected for the absence of lymph node involvement.

RESULTS.

Reduced expression of p27 Kip1 (Յ 50% positive cells) and nuclear p53 accumulation (Ͼ 30% positive cells) were observed in 67 (69.8%) and 9 (9%) tumors, respectively, and were not related to either the pT category or tumor histology. Kaplan-Meier analyses revealed a significant impact on survival by p27 Kip1 (P ϭ 0.0001 by log rank test), p53 (P Ͻ 0.0001) expression, and the pT category (P Ͻ 0.0001). On multivariate analysis, reduced p27 Kip1 protein expression was the strongest independent predictor of reduced survival (P ϭ 0.005; relative risk ϭ 3.348) out weighing the pT category (P ϭ 0.010; relative risk ϭ 2.257) and p53 overexpression (P ϭ 0.016; relative risk ϭ 2.618).

CONCLUSIONS. These data indicated that immunohistochemical detection of p27 Kip1 could help to identify gastric carcinoma patients who are at high risk of death, even in the absence of lymph node involvement, and who might benefit from an adjuvant treatment following surgery.


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