Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8167
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dc.contributor.authorBhargava, Arpit-
dc.contributor.authorPathak, Neelam-
dc.contributor.authorSeshadri, Sriram-
dc.contributor.authorBunkar, Neha-
dc.contributor.authorMishra, Dinesh Kumar-
dc.contributor.authorLohiya, Nirmal Kumar-
dc.contributor.authorMishra, Pradyumna Kumar-
dc.date.accessioned2019-02-04T04:33:17Z-
dc.date.available2019-02-04T04:33:17Z-
dc.date.issued2017-11-24-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/8167-
dc.descriptionAnti-Cancer Agents in Medicinal Chemistry, 2018, 18, 000-000;DOI:10.2174/1871520618666171229223919en_US
dc.description.abstractAbstract: Background: Novel bioactive plant secondary metabolites, including flavonoids, offer a spectrum of chemo-protective responses against a range of human tumor models. However, the clinical translation of these promising anti-cancer agents has been hindered largely by their poor solubility, rapid metabolism, or a combination of both, ultimately resulting in poor bioavailability upon oral administration. Objective: To circumvent the challenges associated with herbal drug development and for effective integration into clinical setting, nano-engineering is one of the emerging pragmatic strategies which has promise to deliver therapeutic concentrations of bio-actives upon oral administration. Method: We assessed the nano-encapsulated flavonoid-rich fraction isolated from a traditional Indian herb Selaginella bryopteris (Sanjeevani) (NP.SB). Both in vitro and in vivo studies were performed to evidence the epigenetic protection mechanisms of NP.SB through a mitochondrial-targeted pre-clinical validation strategy. Results: The mito-protective activity of NP.SB revealed a dose-dependent effect when tested in GC-1 spg (mouse spermatogonial epithelial) and B/CMBA.Ov (mouse ovarian epithelial) following exposure to Nsuccinimidyl N-methylcarbamate, a potential human carcinogen. Smaller size, rapid internalization, faster mobility and site specific delivery conferred significant cancer protection in cultured cells. Notably, this encapsulated flavonoid supplementation; prevented emergence of neoplastic daughter clones from senescent mother phenotypes in pro-oxidant treated GC-1 spg and B/CMBA.Ov cells by selective abrogation of mitochondrial oxidative stress-induced aberrant epigenetic modifications. In vivo studies using a diethylnitrosamine and 2-acetylaminofluorene mouse model demonstrated that NP.SB has a significant inhibitory effect on tumor growth which clearly substantiated our in vitro findings. Conclusion: Anti-carcinogenic property in conjunction with low toxicity of NP.SB, underscores the translational significance of dietary flavonoids as cancer-protective agents for preferential application in clinical settings.en_US
dc.language.isoen_USen_US
dc.publisherBentham Science Publishers;Anti-Cancer Agents in Medicinal Chemistry,en_US
dc.subjectFaculty Paperen_US
dc.subjectFaculty Paper, Scienceen_US
dc.subjectScience, Faculty Paperen_US
dc.subjectCancer preventionen_US
dc.subjectanti-cancer agentsen_US
dc.subjectepigenetic modifieren_US
dc.subjectisocyanateen_US
dc.subjecttranslational oncologyen_US
dc.titlePre-clinical Validation of Mito-targeted Nano-engineered Flavonoids Isolated From Selaginella bryopteris (Sanjeevani) As A Novel Cancer Prevention Strategyen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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