| Literature DB >> 31605713 |
Pranesh Kumar1, Aakriti Agarwal1, Ashok K Singh1, Anurag Kumar Gautam1, Sreemoyee Chakraborti2, Umesh Kumar2, Dinesh Kumar2, Bolay Bhattacharya3, Parthasarathi Panda4, Biswajit Saha5, Tabish Qidwai6, Biswanath Maity2, Sudipta Saha7.
Abstract
Hepatocellular carcinoma (HCC) is one of the most common cancers worldwideand haslimited treatment options. In view of this, zafirlukast (ZAF) was administered orally to DEN-induced HCC rats to evaluate its antineoplastic properties. ELISA, qRT-PCR and Western blot were used to determine the molecular mechanism associated with ZAF therapy for HCC. We found that HCC developed as a result of lower expression of caspases 3 and 9, but their levels returned to normal when the expression of eNOS, BAX, BAD, and Cyt C was decreased and when the expression of iNOS, Bcl-xl, and Bcl-2 was increased. Again, ZAF (80 mg/kg dose) treatment normalized the expression of caspase-mediated apoptotic factors, i.e. BAX and Bcl-2 proteins, as established through Western blot analysis. Later, 1H NMR-based serum metabolomics study revealed that levels of perturbed metabolites in DEN-induced rat serum returned to normal after ZAF administration. Altogether, the antineoplastic potential of ZAF was found to be comparable, and to some degree better, than the marketed chemotherapeutic 5-flurouracil, which may be beneficial for anti-HCC treatment from a future drug design perspective.Entities:
Keywords: (1)H-NMR based metabolomics; Apoptosis; Bcl-2 and BAX proteins; Hepatocellular carcinoma; Zafirlukast
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Year: 2019 PMID: 31605713 DOI: 10.1016/j.yrtph.2019.104489
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271