Background: Metronidazole (MTZ) is a synthetic derivative of nitroimidazole that has been widely used
for the treatment of several bacterial and parasitic infections including trichomoniasis, amoebiasis, giardiasis, liver
abscess, gingivitis, syphilis and phagedena. Scientists have evaluated its carcinogenicity in preclinical in vitro and
in vivo studies.
Method: Google scholar and Pubmed search engines were used to construct historic timeline after discovery of MTZ
with a journey of ~3 decades of research. Similar search was conducted for its in-vivo carcinogenic activities, further
extended 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 a
variety 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 as
a 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 from
MTZ 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 food
products 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.