TY - JOUR
T1 - Prognostic value of p53 protein expression for patients with gastric cancer
T2 - A multivariate analysis
AU - Maehara, Y.
AU - Tomoda, M.
AU - Hasuda, S.
AU - Kabashima, A.
AU - Tokunaga, E.
AU - Kakeji, Y.
AU - Sugimachi, K.
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan and a public trust fund for the promotion of surgery. We thank M Ohara for comments and H Baba, Y Matsuo and J Tsuchihashi for technical assistance.
PY - 1999
Y1 - 1999
N2 - Mutations in the p53 gene, one of the most common genetic alterations in human cancer, are implicated in tumorigenesis and tumour progression. Although p53 protein expression appears to be correlated to prognosis in patients with malignancy, its prognostic role in gastric cancer has remained controversial. We examined the clinical significance of p53 overexpression in 427 patients with gastric cancer, using multivariate analysis. Tumour sections of gastric cancer tissues from these 427 Japanese patients were stained immunohistochemically with monoclonal antibody PAb1801. The presence of p53 expression was statistically compared with clinicopathological features and postoperative survival, using univariate and muitivariate analyses. p53 expression was detected in 38.6% (165 out of 427) of these gastric cancers and immunoreactivity was not observed in normal mucosa adjacent to the tumour. A higher rate of p53 detection was observed among large tumours and in those with a prominent depth of invasion, lymphatic and vascular invasion and lymph node involvement. Prognosis was significantly worse for patients with p53-positive-staining tumours. The 5-year survival rate was 62.5% for patients with p53-negative tumours and 43.3% for those with positive malignancies. p53 expression was a significant prognostic factor for node-positive gastric cancers in subjects undergoing treatment with curative resection, as assessed by Cox regression analysis. Thus, the expression of p53 was closely related to the potential for tumour advance and a poorer post-operative prognosis for patients with gastric cancer.
AB - Mutations in the p53 gene, one of the most common genetic alterations in human cancer, are implicated in tumorigenesis and tumour progression. Although p53 protein expression appears to be correlated to prognosis in patients with malignancy, its prognostic role in gastric cancer has remained controversial. We examined the clinical significance of p53 overexpression in 427 patients with gastric cancer, using multivariate analysis. Tumour sections of gastric cancer tissues from these 427 Japanese patients were stained immunohistochemically with monoclonal antibody PAb1801. The presence of p53 expression was statistically compared with clinicopathological features and postoperative survival, using univariate and muitivariate analyses. p53 expression was detected in 38.6% (165 out of 427) of these gastric cancers and immunoreactivity was not observed in normal mucosa adjacent to the tumour. A higher rate of p53 detection was observed among large tumours and in those with a prominent depth of invasion, lymphatic and vascular invasion and lymph node involvement. Prognosis was significantly worse for patients with p53-positive-staining tumours. The 5-year survival rate was 62.5% for patients with p53-negative tumours and 43.3% for those with positive malignancies. p53 expression was a significant prognostic factor for node-positive gastric cancers in subjects undergoing treatment with curative resection, as assessed by Cox regression analysis. Thus, the expression of p53 was closely related to the potential for tumour advance and a poorer post-operative prognosis for patients with gastric cancer.
UR - http://www.scopus.com/inward/record.url?scp=0032983645&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032983645&partnerID=8YFLogxK
U2 - 10.1038/sj.bjc.6690201
DO - 10.1038/sj.bjc.6690201
M3 - Article
C2 - 10098768
AN - SCOPUS:0032983645
SN - 0007-0920
VL - 79
SP - 1255
EP - 1261
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 7-8
ER -