Tobi M, Darmon E, Rozen P, Avigdor S, Rattan J, Santo M, Barnea E R
Dept. of Gastroenterology, Tel Aviv Medical Center, Israel.
Scand J Gastroenterol. 1993 Nov;28(11):958-62. doi: 10.3109/00365529309098291.
The transformation of xenobiotics and endogenous compounds to active carcinogens and their subsequent deactivation as an aid to eradication may be important in the etiology of some gastrointestinal cancers. In mammals the gastrointestinal tract has been shown to be an important site of inducible enzyme systems active in mucosal biotransformation, but few data are available in man. The mucosal activity of CYPIA1 (formerly aryl hydrocarbon hydroxylase), a potential carcinogen-activating enzyme, and catechol-O-methyl transferase, a potential carcinogen-inactivating enzyme were determined in colonic tissue obtained by biopsy. There were no significant differences in activity rates in normal mucosa between colorectal cancer and healthy persons, but significant differences are seen in patients with a history of neoplasia with no evidence of recurrence. The levels of activity of these carcinogen-inductive and -protective enzymes may be prognostic markers, in that the balance or imbalance could play a role in the recurrence of neoplasia. This will require confirmation and prospective studies.
外源性物质和内源性化合物转化为活性致癌物以及随后为辅助消除而进行的失活,在某些胃肠道癌症的病因学中可能很重要。在哺乳动物中,胃肠道已被证明是参与黏膜生物转化的诱导酶系统的重要部位,但人类方面的数据很少。通过活检获取的结肠组织中,测定了潜在致癌物激活酶CYPIA1(以前称为芳烃羟化酶)和潜在致癌物失活酶儿茶酚-O-甲基转移酶的黏膜活性。结直肠癌患者与健康人的正常黏膜活性率无显著差异,但在有肿瘤病史且无复发证据的患者中可见显著差异。这些致癌物诱导和保护酶的活性水平可能是预后标志物,因为这种平衡或失衡可能在肿瘤复发中起作用。这需要进一步证实和前瞻性研究。