The DCC protein and prognosis in colorectal cancer

被引:237
作者
Shibata, D
Reale, MA
Lavin, P
Silverman, M
Fearon, ER
Steele, G
Jessup, JM
Loda, M
Summerhayes, IC
机构
[1] HARVARD UNIV, NEW ENGLAND DEACONESS HOSP,SCH MED,DEPT SURG, LAB CANC BIOL, BOSTON, MA 02215 USA
[2] HARVARD UNIV, NEW ENGLAND DEACONESS HOSP, SCH MED, DEPT PATHOL, BOSTON, MA 02215 USA
[3] YALE UNIV, SCH MED, SECT MED ONCOL, NEW HAVEN, CT USA
[4] BOSTON BIOSTAT RES FDN, FRAMINGHAM, MA USA
[5] LAHEY HITCHCOCK MED CTR, DEPT PATHOL, BURLINGTON, MA USA
[6] UNIV MICHIGAN, MED CTR, DEPT INTERNAL MED, DIV MED & MOL GENET, ANN ARBOR, MI 48109 USA
关键词
D O I
10.1056/NEJM199612053352303
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Allelic loss of chromosome 18q predicts a poor outcome in patients with stage II colorectal cancer. Although the specific gene inactivated by this allelic loss has not been elucidated, the DCC (deleted in colorectal cancer) gene is a candidate. We investigated whether the expression of the DCC protein in tumor cells is a prognostic marker in colorectal carcinoma. Methods The expression of DCC was evaluated immunohistochemically in 132 paraffin-embedded samples from patients with curatively resected stage II or III colorectal carcinomas. The Cox proportional-hazards model was used to adjust for covariates including age, sex, tumor site, degree of tumor differentiation, and use of adjuvant therapy. Results The expression of DCC was a strong positive predictive factor for survival in both stage II and stage III colorectal carcinomas. In patients with stage II disease whose tumors expressed DCC, the five-year survival rate was 94.3 percent, whereas in patients with DCC-negative tumors, the survival rate was 61.6 percent (P<0.001). In patients with stage III disease, the respective survival rates were 59.3 percent and 33.2 percent (P = 0.03). Conclusions DCC is a prognostic marker in patients with stage II or stage III colorectal cancer. In stage II colorectal carcinomas, the absence of DCC identifies a subgroup of patients with lesions that behave like stage III cancers. These findings may thus have therapeutic implications in this group of (C) 1996, Massachusetts Medical Society.
引用
收藏
页码:1727 / 1732
页数:6
相关论文
共 47 条
  • [1] [Anonymous], 1984, NEW ENGL J MED, V310, P737
  • [2] BRABANT G, 1993, CANCER RES, V53, P4987
  • [3] SOMATIC ALLELIC LOSS AT THE DCC, APC, NM23-H1 AND P53 TUMOR-SUPPRESSOR GENE LOCI IN HUMAN PROSTATIC-CARCINOMA
    BREWSTER, SF
    BROWNE, S
    BROWN, KW
    [J]. JOURNAL OF UROLOGY, 1994, 151 (04) : 1073 - 1077
  • [4] LOSS OF HETEROZYGOSITY ON CHROMOSOME 18Q IS ASSOCIATED WITH MUSCLE-INVASIVE TRANSITIONAL-CELL CARCINOMA OF THE BLADDER
    BREWSTER, SF
    GINGELL, JC
    BROWNE, S
    BROWN, KW
    [J]. BRITISH JOURNAL OF CANCER, 1994, 70 (04) : 697 - 700
  • [5] BROWN RW, 1995, MODERN PATHOL, V8, P515
  • [6] UNC-40, a C-elegans homolog of DCC (Deleted in Colorectal Cancer), is required in motile cells responding to UNC-6 netrin cues
    Chan, SSY
    Zheng, H
    Su, MW
    Wilk, R
    Killeen, MT
    Hedgecock, EM
    Culotti, JG
    [J]. CELL, 1996, 87 (02) : 187 - 195
  • [7] THE DCC GENE - STRUCTURAL-ANALYSIS AND MUTATIONS IN COLORECTAL CARCINOMAS
    CHO, KR
    OLINER, JD
    SIMONS, JW
    HEDRICK, L
    FEARON, ER
    PREISINGER, AC
    HEDGE, P
    SILVERMAN, GA
    VOGELSTEIN, B
    [J]. GENOMICS, 1994, 19 (03) : 525 - 531
  • [8] CDCC (CHICKEN HOMOLOG TO A GENE DELETED IN COLORECTAL-CARCINOMA) IS AN EPITHELIAL ADHESION MOLECULE EXPRESSED IN THE BASAL CELLS AND INVOLVED IN EPITHELIAL-MESENCHYMAL INTERACTION
    CHUONG, CM
    JIANG, TX
    YIN, E
    WIDELITZ, RB
    [J]. DEVELOPMENTAL BIOLOGY, 1994, 164 (02) : 383 - 397
  • [9] Cordon-Cardo C, 1994, Important Adv Oncol, P71
  • [10] COX DR, 1972, J R STAT SOC B, V34, P187