FREE-RADICALS AND THE ETIOLOGY OF COLON CANCER

被引:301
作者
BABBS, CF
机构
[1] Biomedical Engineering Center, Purdue University, West Lafayette, IN 47907, Potter Building
关键词
Benzo(a)pyrene; Bile salts; Bilirubin; Carcinogenesis; Colon carcinoma; Fenton reaction; Free radicals; Hydroxyl radical; Iron; Superoxide;
D O I
10.1016/0891-5849(90)90091-V
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This hypothesis paper reviews diverse evidence suggesting that intracolonic production of oxygen radicals may play a role in carcinogenesis. The hypothesis began to evolve when the author made the chance discovery that 1/10,000 dilutions of feces generated detectable quantities of highly reactive hydroxyl radicals (HO·). The rate of HO· formation, detected using DMSO as a molecular probe, was quite remarkable, corresponding to that which would be produced by over 10,000 rads of gamma irradiation per day, absorbed in the periphery of the fecal mass adjacent to the mucosa. The relatively high concentrations of iron in feces, together with the ability of bile pigments to act as iron chelators that support Fenton chemistry, may very well permit efficient HO· generation from superoxide and hydrogen peroxide produced by bacterial metabolism. Such free radical generation in feces could provide a missing link in our understanding of the etiology of colon cancer: the oxidation of procarcinogens either by fecal Ho·, or by secondary peroxyl radicals (ROO·) to form active carcinogens or mitogenic tumor promotors. Intracolonic free radical formation may explain the high incidence of cancer in the colon and rectum, compared to other regions of the GI tract, as well as the observed correlations of a higher incidence of colon cancer with red meat in the diet, which increases stool iron, and with excessive fat in the diet, which may increase the fecal content of procarcinogens and bile pigments. © 1990.
引用
收藏
页码:191 / 200
页数:10
相关论文
共 90 条
  • [21] Nagata, Kodama, Ioki, Kumura, Free radicals produced from cheimical carcinogens and their significance in carcinogenesis, Free radicals and cancer, (1982)
  • [22] Dix, Marnett, Metabolism of polycyclic aromatic hydrocarbon derivatives to ultimate carcinogens during lipid peroxidation, Science, 221, pp. 77-79, (1983)
  • [23] Marnett, Hydroperoxide-dependent oxygenation of polycyclic aromatic hydrocarbons and their metabolites, Polycyclic hydrocarbons and carcinogenesis, pp. 307-326, (1985)
  • [24] Marnett, Reed, Dennison, Prostaglandin synthetase dependent activation of 7,8-dihydro-7,8-dihydroxybenzo(a)pyrene to mutagenice derivatives, Biochem. Biophys. Res. Commun., 82, pp. 210-216, (1978)
  • [25] Dix, Marnett, Free radical epoxidation of 7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene by hematin and polyunsaturated fatty acid hydroperoxides, J. Am. Chem. Soc., 103, pp. 6744-6746, (1981)
  • [26] Eling, Curtis, Battista, Marnett, Oxidation of (+)-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene by mouse keratinocytes: evidence for peroxyl radical- and monoxygenase-dependent metatolism, Carcinogenesis, 7, pp. 1957-1963, (1986)
  • [27] Walling, Free radicals in solution, (1957)
  • [28] Mayo, Fee-radical autoxidations of hydrocarbons, Accounts Chem. Res., 1, pp. 193-201, (1968)
  • [29] Robertson, Sivarajah, Eling, Zeigler, Activation of some aromatic amines to mutagenic products by prostaglandin endoperoxide synthetase, Cancer Res., 43, pp. 476-480, (1983)
  • [30] Sammons, Vaughan, Frazer, Synthesis of long-chain fats by bacteria isolated from human feces, Nature, 177, (1956)