Evaluation of malignancy and the prognosis of esophageal cancer based on an immunohistochemical study (p53, E-cadherin, epidermal growth factor receptor)

被引:66
作者
Inada, S [1 ]
Koto, T [1 ]
Futami, K [1 ]
Arima, S [1 ]
Iwashita, A [1 ]
机构
[1] Fukuoka Univ, Sch Med, Chikushi Hosp, Dept Surg, Chikushino, Fukuoka 8188502, Japan
来源
SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY | 1999年 / 29卷 / 06期
关键词
p53; E-cadherin; epidermal growth factor receptor; esophageal cancer;
D O I
10.1007/BF02482343
中图分类号
R61 [外科手术学];
学科分类号
摘要
The subjects in this study consisted of 40 preoperative untreated esophageal squamous cell carcinoma patients. While p53 did not significantly correlate with the clinicopathological factors, E-cadherin significantly correlated with lymphatic invasion, vascular invasion, the depth of invasion, the degree of lymph node metastasis, the histological stage, and the number of lymph node metastases, Epidermal growth factor receptor (EGFR) significantly correlated with age, the depth of invasion, and the number of lymph node metastases. The 5-year cumulative survival rate was 45.7% in the p53-positive cases and 61.9% in the p53-negative cases with no significant difference, and 87.8% in the E-cadherin-positive cases and 19.1% in the -negative cases, and the difference was significant. The prognosis was significantly poor in EGFR-positive subjects: the 5-year survival rate was 38.6% in EGFR-positive cases and 68% in -negative cases. The 5-year survival rate in E-cadherin-negative, EGFR-positive cases was 0%, while it was 91.7% in the reverse pattern, and this difference was significant, These findings suggest that both E-cadherin and EGFR are important prognostic factors, and a more precise prognosis can thus be obtained by combining them, Such a combined technique may be very useful as an indicator for grading the biological malignancy of esophageal cancer.
引用
收藏
页码:493 / 503
页数:11
相关论文
共 26 条
  • [1] Arai M, 1994, Nihon Geka Gakkai Zasshi, V95, P171
  • [2] COHEN S, 1982, J BIOL CHEM, V257, P1523
  • [3] COX DR, 1972, J R STAT SOC B, V34, P187
  • [4] ACTIVATING MUTATIONS FOR TRANSFORMATION BY P53 PRODUCE A GENE-PRODUCT THAT FORMS AN HSC70-P53 COMPLEX WITH AN ALTERED HALF-LIFE
    FINLAY, CA
    HINDS, PW
    TAN, TH
    ELIYAHU, D
    OREN, M
    LEVINE, AJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (02) : 531 - 539
  • [5] DIFFERENT STEM-CELL POPULATIONS IN MOUSE EPIDERMIS AND LINGUAL EPITHELIUM
    FUKUDA, M
    OKAMURA, K
    FUJITA, S
    BOHM, N
    ROHRBACH, R
    SANDRITTER, W
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 1978, 163 (03) : 205 - 227
  • [6] DETECTION OF EPIDERMAL GROWTH-FACTOR RECEPTORS AND E-CADHERINS IN THE BASOLATERAL MEMBRANE OF A431 CELLS BY LASER SCANNING FLUORESCENCE MICROSCOPY
    FUKUYAMA, R
    SHIMIZU, N
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 1991, 82 (01): : 8 - 11
  • [7] GOUKON Y, 1994, ANTICANCER RES, V14, P1305
  • [8] HOLLSTEIN MC, 1991, CANCER RES, V51, P4102
  • [9] FREQUENT MUTATION OF THE P53 GENE IN HUMAN ESOPHAGEAL CANCER
    HOLLSTEIN, MC
    METCALF, RA
    WELSH, JA
    MONTESANO, R
    HARRIS, CC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) : 9958 - 9961
  • [10] ITAKURA Y, 1993, SHOKAKIGAN NO HASSEI, V5, P195