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Association of Metronidazole with Cancer: A Potential Risk Factor or Inconsistent Deductions?

机译:甲硝唑与癌症结合:潜在的危险因素或扣除不一致?

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Background: Metronidazole (MTZ) is a synthetic derivative of nitroimidazole that has been widely usedfor the treatment of several bacterial and parasitic infections including trichomoniasis, amoebiasis, giardiasis, liverabscess, gingivitis, syphilis and phagedena. Scientists have evaluated its carcinogenicity in preclinical in vitro andin vivo studies.Method: Google scholar and Pubmed search engines were used to construct historic timeline after discovery of MTZwith a journey of ~3 decades of research. Similar search was conducted for its in vivo carcinogenic activities, furtherextended to elaborate its role in carcinogenicity in humans.Results: In addition to preclinical in vitro validation of DNA damage, MTZ has been reported to induce cancer in avariety of animal models including lung cancer, malignant lymphomas, breast cancer, hepatocellular carcinoma,pituitary tumors, testicular neoplasms and uterine cancer. Several retrospective cohort studies have reported MTZ asa potential risk factor for lung cancer (n = 771), cervical cancer (n = 2500), breast cancer (n = 2), cholangiocarcinoma(n = 1), and neuroblastoma (n = 28). So far, all the reported data have confirmed MTZ carcinogenicity in animals;however it is still controversial in humans. Based on previous observations, the oxidative metabolites fromMTZ are shown to have more carcinogenic effects than the parent drug itself.Conclusion: Due to potent carcinogenic behaviour, use of MTZ for animals’ treatment and its uses in animal foodproducts is prohibited in USA and European countries; however its clinical use in human population is still increasing.Therefore, regular research studies are required to explicate its mechanism/s involved in carcinogenesis.
机译:背景技术甲硝唑(MTZ)是硝基咪唑的合成衍生物,已广泛用于治疗几种细菌和寄生虫感染,包括滴虫病,阿米巴病,贾奈多,肝脏,牙龈炎,梅毒和植物。科学家在临床前在体外评估了其致癌性和体内研究。方法:谷歌学者和PubMed搜索引擎被用来在发现MTZWith〜3年的研究之旅后建造历史时间表。在体内致癌活动中进行了类似的搜索,令人遗憾的是在人类中阐述其在致癌性中的作用。结果:除了临床前的DNA损伤的体外验证外,MTZ均据报道,患有肺癌的动物模型的令人费解的癌症,恶性淋巴瘤,乳腺癌,肝细胞癌,垂体肿瘤,睾丸瘤和子宫癌。几个回顾性队列研究报告了MTZ ASA肺癌潜在危险因素(n = 771),宫颈癌(n = 2500),乳腺癌(n = 2),胆管癌(n = 1)和神经母细胞瘤(n = 28) 。到目前为止,所有报告的数据都证实了动物中的MTZ致癌性;然而,人类仍然存在争议。基于先前的观察结果,来自MMTZ的氧化代谢物比母体药物本身具有更多的致癌作用。结论:由于有效的致癌行为,美国和欧洲国家禁止使用MTZ进行动物的治疗及其在动物食品中的用途;然而,它在人口中的临床应用仍在增加。因此,需要定期研究旨在突出其参与致癌作用的机制。

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