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三种将胆汁与胃肠道致癌作用联系起来的假说:某些胆汁盐具有可用于辅助化疗的特性。

Three hypotheses linking bile to carcinogenesis in the gastrointestinal tract: certain bile salts have properties that may be used to complement chemotherapy.

作者信息

Stamp Dennis H

机构信息

Ontario, Canada.

出版信息

Med Hypotheses. 2002 Oct;59(4):398-405. doi: 10.1016/s0306-9877(02)00125-1.

Abstract

The literature for the proliferative effect of bile acids on the GI tract has been reviewed and three hypotheses developed regarding their carcinogenicity. Considered as a unit, the GI tract is protected from this carcinogenicity in different ways in the esophagus, stomach, small bowel and colon. Uncharged BAs can enter the esophageal epithelial cells by reflux of gastroduodenal juices in humans, and in animals by surgical alteration of the GI tract or by adding bile concentrate to the diets, and this can initiate GERD and eventually cancer. Acid suppressant therapy used to treat GERD patients, converts stomach pH to >4. This will remove the charges on conjugated bile acids allowing them entry into the epithelium thus casting doubt on the efficacy of acid suppression. From these observations, we postulate that (a) uncharged BA in daily contact with the esophagus can cause GERD and eventually cancer. This might explain the cancers obtained by Fein et al. (b) Clinical trials designed to test the effectiveness of acid suppressants will be meaningless since up to approximately 87% of these patients (in one study) have bile in their refluxate, and this, combined with acid suppressants, will initiate carcinogenesis. (c) Bile reaching a colon made sterile by antibiotics or other means, will not be deconjugated and so, with pKa's of 2 and 4, will be uncharged and therefore can easily enter the colonic cells where the pH is >6. This should be of some concern, especially on a high-fat diet when more bile enters the colon. A group of physicians noted that approximately 47% of patients with esophageal cancers also had some form of colon cancer and postulated that an etiological factor in the environment was responsible. Could this factor be bile? Reactions of certain bile salts with epithelial cells suggest a useful role for them in chemotherapy. Experiments to test hypotheses a, b and c are presented in the addendum.

摘要

关于胆汁酸对胃肠道的增殖作用的文献已被综述,并就其致癌性提出了三种假说。作为一个整体来看,胃肠道在食管、胃、小肠和结肠中以不同方式免受这种致癌性影响。未带电荷的胆汁酸可通过人胃十二指肠液反流进入食管上皮细胞,在动物中则可通过胃肠道手术改变或在饮食中添加胆汁浓缩物进入,这可引发胃食管反流病(GERD)并最终导致癌症。用于治疗GERD患者的抑酸疗法会使胃内pH值升至>4。这会去除结合型胆汁酸上的电荷,使其能够进入上皮细胞,从而使人对抑酸疗法的疗效产生怀疑。基于这些观察结果,我们推测:(a)每天与食管接触的未带电荷的胆汁酸可导致GERD并最终引发癌症。这或许可以解释Fein等人所观察到的癌症情况。(b)旨在测试抑酸剂有效性的临床试验将毫无意义,因为在一项研究中,高达约87%的此类患者的反流物中含有胆汁,而这与抑酸剂共同作用会引发致癌作用。(c)通过抗生素或其他手段使结肠无菌后,到达结肠的胆汁将不会被去结合,因此,其pKa值分别为2和4,将处于未带电荷状态,从而能够轻易进入pH值>6的结肠细胞。这一点应引起一定关注,尤其是在高脂饮食时,会有更多胆汁进入结肠。一组医生指出,约47%的食管癌患者同时还患有某种形式的结肠癌,并推测环境中的一个病因因素与此有关。这个因素会是胆汁吗?某些胆汁盐与上皮细胞的反应表明它们在化疗中可能发挥有益作用。附录中展示了用于验证假说a、b和c的实验。

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