Overexpression of p53 is not associated with drug resistance of gastric cancers to 5-fluorouracil-based systemic chemotherapy
Journal
Hepato-Gastroenterology
Journal Volume
46
Journal Issue
25
Pages
610-615
Date Issued
1999
Author(s)
Abstract
BACKGROUND/AIMS: Recent in vitro evidence has strongly suggested that most anti-cancer drugs exert their cytotoxic effects via a p53-dependent apoptosis pathway. An intact p53 molecule appears to be a prerequisite for the cancer cells to be susceptible to these drugs. In this study, we specifically examined if overexpression of p53 may confer drug resistance on human gastric cancer. METHODOLOGY: All patients were treated by an empirical HDFL regimen (weekly 24-hour infusion of 5-FU, 2600 mg/m2 and leucovorin, 300 mg/m2) in a prospective phase II clinical trial. Among them, patients with adequate pre-chemotherapy gastric cancer tissues for immunohistochemical studies were selected for this study. A p53 DO7 monoclonal antibody was used to detect the overexpression of p53. The results were designated as '-' or '+' by the independent interpretation of two pathologists. RESULTS: A total of 30 patients, 18 men and 12 women, with a median age of 61.5 years (range: 32-78 years), were studied. There were 15 responders and 15 non-responders to HDFL chemotherapy. The percentage of p53 overexpression with positive DO7 staining was 20.0% (6 out of 30). There were no significant differences in the pertinent clinicopathologic features between the patients with positive staining of p53 and the patients with negative staining of p53. Three out of 6 (50.0%) patients with positive staining of p53 and 12 out of 24 (50.0%) patients with negative staining of p53 responded to chemotherapy, respectively (p = 1.000 by Fisher's exact test). CONCLUSIONS: Our data suggested that the overexpression of p53 does not predict drug resistance to 5-FU of human gastric cancer.
SDGs
Other Subjects
antineoplastic agent; fluorouracil; folinic acid; monoclonal antibody; protein p53; adult; aged; article; cancer combination chemotherapy; clinical article; clinical trial; drug resistance; female; human; human tissue; immunohistochemistry; male; phase 2 clinical trial; priority journal; prospective study; protein expression; stomach cancer; tumor resistance; Adenocarcinoma; Adult; Aged; Antibodies, Monoclonal; Antimetabolites, Antineoplastic; Clinical Trials, Phase II; Drug Resistance, Neoplasm; Female; Fluorouracil; Humans; Male; Middle Aged; Prospective Studies; Stomach Neoplasms; Tumor Suppressor Protein p53
Type
journal article