The cause of colorectal cancer

被引:27
作者
de Leon, MP [1 ]
Roncucci, L [1 ]
机构
[1] Univ Modena, Dept Internal Med, I-41100 Modena, Italy
来源
DIGESTIVE AND LIVER DISEASE | 2000年 / 32卷 / 05期
关键词
adenoma; cancer; colon; FAP; HNPCC; microsatellite instability; polyp;
D O I
10.1016/S1590-8658(00)80265-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer continues to represent one of the major causes of cancer-related morbidity in all western countries. A review has been made of the main aetiological factors which have been related to colorectal cancer development with particular attention being focused on: a) new advancements in molecular biology, and b) the interaction between genetic predisposition and environmental factors. Worldwide, approximately 900,000 cases of colorectal malignancies have been diagnosed in 1996 and this accounts for 8.5% of all new Gases of cancer. Crude incidence rates range from 0.6-5.0 cases/100,000/year in Senegal and India to 50-70 cases in developed countries. Environmental factors, such as meat, saturated fat, low physical activity, obesity, smoking, alcoholic beverages, and inflammatory bowel diseases seem to increase the risk of colorectal cancer. in contrast, fruit, vegetables, fibre, antioxidant vitamins, calcium, folate, physical exercise and non-steroidal anti-inflammatory drugs seem to show a protective effect. For some of these factors, the molecular basis of their mechanism of action begins to be elucidated. Colorectal cancer develops from benign precursors, the adenomatous polyps; there is extensive evidence that polyps transform into cancer in a stepwise manner, and that several molecular abnormalities (mutations of oncogenes, inactivation of tumour suppressor genes and microsatellite instability) accompany and, somehow, determine colorectal tumourigenesis. Two major Hereditary Colorectal Cancer syndromes - Familial Adenomatous Polyposis and Hereditary Non-polyposis Colorectal Cancer - have been described and characterized st molecular levels; it is estimated that these inherited conditions might account for up to 5% of all large bowel malignancies. Familial colorectal cancer remains undefined and is presumably due to multifactorial inheritance. Recently, identified germline mutations (such as /1307K in the APC gene) might account for a fraction of these familial cases, at least in some populations. At variance with many other tumours, the aetiology and pathogenesis of colorectal cancer have been partially clarified, so that we are now in the position to take preventive measures and to design surveillance programmes which might lead to a certain reduction in incidence and mortality. However, since many of the aetiological factors are strictly related to modern customs and lifestyle, they will be difficult to eradicate; this awareness should stimulate further investigations in this exciting field of research.
引用
收藏
页码:426 / 439
页数:14
相关论文
共 169 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]  
[Anonymous], DIET NUTR PREV CANC
[4]   Calcium supplements for the prevention of colorectal adenomas [J].
Baron, JA ;
Beach, M ;
Mandel, JS ;
van Stolk, RU ;
Haile, RW ;
Sandler, RS ;
Rothstein, R ;
Summers, RW ;
Snover, DC ;
Beck, GJ ;
Bond, JH ;
Greenberg, ER .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (02) :101-107
[5]   TRENDS IN RIGHT AND LEFT-SIDED COLON CANCER [J].
BEART, RW ;
MELTON, LJ ;
MARUTA, M ;
DOCKERTY, MB ;
FRYDENBERG, HB ;
OFALLON, WM .
DISEASES OF THE COLON & RECTUM, 1983, 26 (06) :393-398
[6]  
Bellacosa A, 1996, AM J MED GENET, V62, P353, DOI 10.1002/(SICI)1096-8628(19960424)62:4<353::AID-AJMG7>3.0.CO
[7]  
2-S
[8]   MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 [J].
Bellacosa, A ;
Cicchillitti, L ;
Schepis, F ;
Riccio, A ;
Yeung, AT ;
Matsumoto, Y ;
Golemis, EA ;
Genuardi, M ;
Neri, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3969-3974
[9]   TUMOR SPECTRUM IN HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER (HNPCC) AND IN FAMILIES WITH SUSPECTED HNPCC - A POPULATION-BASED STUDY IN NORTHERN ITALY [J].
BENATTI, P ;
SASSATELLI, R ;
RONCUCCI, L ;
PEDRONI, M ;
FANTE, R ;
DIGREGORIO, C ;
LOSI, L ;
GELMINI, R ;
DELEON, MP .
INTERNATIONAL JOURNAL OF CANCER, 1993, 54 (03) :371-377
[10]   CONGENITAL HYPERTROPHY OF THE RETINAL-PIGMENT EPITHELIUM AS A MARKER FOR FAMILIAL ADENOMATOUS POLYPOSIS [J].
BERK, T ;
COHEN, Z ;
MCLEOD, RS ;
PARKER, JA .
DISEASES OF THE COLON & RECTUM, 1988, 31 (04) :253-257