Molecular oncology in pancreatic cancer

被引:36
作者
Gansauge, S [1 ]
Gansauge, F [1 ]
Beger, HG [1 ]
机构
[1] UNIV ULM, DEPT GEN SURG, D-89075 ULM, GERMANY
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1996年 / 74卷 / 06期
关键词
pancreas; cancer; genes; growth factors; tumor markers;
D O I
10.1007/s001090050032
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cancer of the pancreas still has a very poor prognosis despite improved diagnostic methods and therapeutic regimens. The reasons for the aggressiveness of this cancer are not known, and the molecular mechanisms that govern the growth of pancreatic cancer cells are still not clearly defined. During the past two decades the development of new molecular biological techniques has offered new perspectives for a better understanding of pancreatic cancer. Tumor markers such as CA19-9 and CEA are used for diagnosis and for following the postoperative course of cancer patients. Characterization of pancreatic cancer cells using several molecular biological techniques has revealed overexpression or altered expression of growth factors and adhesion molecules, implying altered cell-cell and growth-regulatory interactions. In pancreatic cancer mutations in oncogenes and tumor suppressor genes are frequently detected in p53 and K-ras. This article reviews the possible molecular approaches for diagnosis, prognosis, or even therapy of pancreatic cancer.
引用
收藏
页码:313 / 320
页数:8
相关论文
共 99 条
[21]   ACTIVATING MUTATIONS FOR TRANSFORMATION BY P53 PRODUCE A GENE-PRODUCT THAT FORMS AN HSC70-P53 COMPLEX WITH AN ALTERED HALF-LIFE [J].
FINLAY, CA ;
HINDS, PW ;
TAN, TH ;
ELIYAHU, D ;
OREN, M ;
LEVINE, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (02) :531-539
[22]  
FRIESS H, 1993, CANCER RES, V53, P2704
[23]  
FRIESS H, 1994, AM J PATHOL, V144, P117
[24]   ENHANCED EXPRESSION OF TRANSFORMING GROWTH-FACTOR-BETA ISOFORMS IN PANCREATIC-CANCER CORRELATES WITH DECREASED SURVIVAL [J].
FRIESS, H ;
YAMANAKA, Y ;
BUCHLER, M ;
EBERT, M ;
BEGER, HG ;
GOLD, LI ;
KORC, M .
GASTROENTEROLOGY, 1993, 105 (06) :1846-1856
[25]   CA-494 - A NEW TUMOR-MARKER FOR THE DIAGNOSIS OF PANCREATIC-CANCER [J].
FRIESS, H ;
BUCHLER, M ;
AUERBACH, B ;
WEBER, A ;
MALFERTHEINER, P ;
HAMMER, K ;
MADRY, N ;
GREINER, S ;
BOSSLET, K ;
BEGER, HG .
INTERNATIONAL JOURNAL OF CANCER, 1993, 53 (05) :759-763
[26]  
GANSAUGE S, 1994, PANCREAS, V9, P788
[27]  
GELDER FB, 1978, CANCER RES, V38, P313
[28]  
GONZALEZ AM, 1992, AM J PATHOL, V141, P661
[29]   MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF FIBROBLAST GROWTH-FACTOR, AN ANGIOGENIC FACTOR WHICH ALSO CONTROLS THE PROLIFERATION AND DIFFERENTIATION OF MESODERM AND NEUROECTODERM DERIVED CELLS [J].
GOSPODAROWICZ, D ;
NEUFELD, G ;
SCHWEIGERER, L .
CELL DIFFERENTIATION, 1986, 19 (01) :1-17
[30]   HIGH-FREQUENCY OF KI-RAS CODON-12 MUTATIONS IN PANCREATIC ADENOCARCINOMAS [J].
GRUNEWALD, K ;
LYONS, J ;
FROHLICH, A ;
FEICHTINGER, H ;
WEGER, RA ;
SCHWAB, G ;
JANSSEN, JWG ;
BARTRAM, CR .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (06) :1037-1041