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dc.contributor.authorSingh, Pushpendra
dc.contributor.authorBast, Felix
dc.contributor.authorSingh, Ravi Shankar
dc.date.accessioned2018-01-01T08:52:04Z
dc.date.available2018-01-01T08:52:04Z
dc.date.issued2016
dc.identifier.citationSingh P, Bast F, Singh RS. Natural Compounds Targeting Transforming Growth Factor-β: In Silico and In Vitro Study. Electronic J Biol, 13:1en_US
dc.identifier.issn1860-3122
dc.identifier.urihttp://kr.cup.edu.in/handle/32116/416
dc.description.abstractInhibition of the tumor-promoting effects of transforming growth factor beta receptor (TGFβR) in carcinogenesis provides a better therapeutic intervention. Various natural compounds, inhibitors of TGFβR have been used for in vitro and in vivo anticancer study. Although very few TGFβR inhibitors are now intensifying in preclinical studies. In this study our aim to investigate TGFβR1, TGFβR2 and TAK1 inhibitor by using molecular docking and in vitro study. Our result revealed that some compounds have better docking energy. Moreover, the effect of two lead molecules epigallocatechin gallate (EGCG) and myricetin on the mRNA expression of TGFβR1 was reported after the 48 hrs treatments in HepG2 and PC3 cancer cell lines. The RT-PCR showed that compound EGCG and myricetin reduced the mRNA expression of TGFβR1 at 80 μM concentration. This molecular docking study provides a better understanding of binding of compounds to the active site of proteins and to summarize the various binding energy, hydrophobic, hydrogen, an electrostatic bond that are decisive for the protein-ligand interactions. Further experimental work will be required for validation of our results.en_US
dc.language.isoenen_US
dc.publisherejBioen_US
dc.subjectNatural compoundsen_US
dc.subjectCanceren_US
dc.subjectMaestro 9.6en_US
dc.subjectMolecular dockingen_US
dc.subjectIn vitroen_US
dc.titleNatural Compounds Targeting Transforming Growth Factor-β: In Silico and In Vitro Studyen_US
dc.typeArticleen_US


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