Molecular lesions in colorectal cancer: impact on prognosis? Original data and review of the literature

被引:61
作者
Klump, B
Nehls, O
Okech, T
Hsieh, CJ
Gaco, V
Gittinger, FS
Sarbia, M
Borchard, F
Greschniok, A
Gruenagel, HH
Porschen, R
Gregor, M
机构
[1] Univ Hosp, Dept Internal Med 1, D-72076 Tubingen, Germany
[2] Univ Dusseldorf, Inst Pathol, D-4000 Dusseldorf, Germany
[3] Hosp Aschaffenburg, Inst Pathol, Aschaffenburg, Germany
[4] Univ Tubingen Hosp, Inst Pathol, Tubingen, Germany
[5] Evangel Hosp Dusseldorf, Dept Surg, Dusseldorf, Germany
[6] Cent Hosp Bremen Ost, Dept Internal Med, Bremen, Germany
关键词
colorectal carcinoma; prognosis; molecular biology; p53; DCC;
D O I
10.1007/s00384-003-0499-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. In the Dukes' B and C stages of colorectal carcinoma there are considerable variations in the observed courses of the disease. Since post-operative chemotherapy in patients with Dukes' C (node-positive) colon carcinoma has been demonstrated to be effective in improving overall-survival, a more exact prognosis assessment gains additional significance and therapeutic relevance. Discussion. One also hopes to derive improved prognostic factors from the clarification of the molecular pathogenesis. Because of its frequency and the accessibility and recognizability of its developmental stages colorectal carcinoma is among the best investigated of all solid tumors. Despite a multitude of suggested molecular candidate markers none of these changes has yet been able enter the everyday life of the clinic. However, it is to be expected that some of the molecular alterations presently discussed will gain importance before long in the clinical treatment of patients with colorectal carcinoma. Conclusion. Considering also our own findings, this review presents the latest developments in the scientific discussion of the tumor suppressor/oncogenes p53, k-ras, and DCC, biochemical determinants of the 5-fluorouracil metabolism, and defects of the DNA repair system.
引用
收藏
页码:23 / 42
页数:20
相关论文
共 163 条
[1]  
AALTONEN LA, 1994, CANCER RES, V54, P1645
[2]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[3]  
Ahnen DJ, 1998, CANCER RES, V58, P1149
[4]   Kirsten ras mutations in patients with colorectal cancer: the multicenter "RASCAL" study [J].
Andreyev, HJN ;
Norman, AR ;
Cunningham, D ;
Oates, JR ;
Clarke, PA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (09) :675-684
[5]  
[Anonymous], [No title captured]
[6]  
Aschele C, 2000, CLIN CANCER RES, V6, P4797
[7]   Immunohistochemical quantitation of thymidylate synthase expression in colorectal cancer metastases predicts for clinical outcome to fluorouracil-based chemotherapy [J].
Aschele, C ;
Debernardis, D ;
Casazza, S ;
Antonelli, G ;
Tunesi, G ;
Baldo, C ;
Lionetto, R ;
Maley, F ;
Sobrero, A .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (06) :1760-1770
[8]  
ASCHELE C, 1992, CANCER RES, V52, P1855
[9]  
ASCHELE C, 2000, P AN M AM SOC CLIN, V19, pA251
[10]   OVEREXPRESSION OF P53 AND LONG-TERM SURVIVAL IN COLON-CARCINOMA [J].
AUVINEN, A ;
ISOLA, J ;
VISAKORPI, T ;
KOIVULA, T ;
VIRTANEN, S ;
HAKAMA, M .
BRITISH JOURNAL OF CANCER, 1994, 70 (02) :293-296