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DC Field | Value | Language |
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dc.contributor.author | Bhargava, Arpit | - |
dc.contributor.author | Pathak, Neelam | - |
dc.contributor.author | Seshadri, Sriram | - |
dc.contributor.author | Bunkar, Neha | - |
dc.contributor.author | Mishra, Dinesh Kumar | - |
dc.contributor.author | Lohiya, Nirmal Kumar | - |
dc.contributor.author | Mishra, Pradyumna Kumar | - |
dc.date.accessioned | 2019-02-04T04:33:17Z | - |
dc.date.available | 2019-02-04T04:33:17Z | - |
dc.date.issued | 2017-11-24 | - |
dc.identifier.uri | http://10.1.7.192:80/jspui/handle/123456789/8167 | - |
dc.description | Anti-Cancer Agents in Medicinal Chemistry, 2018, 18, 000-000;DOI:10.2174/1871520618666171229223919 | en_US |
dc.description.abstract | Abstract: 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.iso | en_US | en_US |
dc.publisher | Bentham Science Publishers;Anti-Cancer Agents in Medicinal Chemistry, | en_US |
dc.subject | Faculty Paper | en_US |
dc.subject | Faculty Paper, Science | en_US |
dc.subject | Science, Faculty Paper | en_US |
dc.subject | Cancer prevention | en_US |
dc.subject | anti-cancer agents | en_US |
dc.subject | epigenetic modifier | en_US |
dc.subject | isocyanate | en_US |
dc.subject | translational oncology | en_US |
dc.title | Pre-clinical Validation of Mito-targeted Nano-engineered Flavonoids Isolated From Selaginella bryopteris (Sanjeevani) As A Novel Cancer Prevention Strategy | en_US |
dc.type | Faculty Papers | en_US |
Appears in Collections: | Faculty Papers |
Files in This Item:
File | Description | Size | Format | |
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2018 Bhargava et al., 2018.pdf | Bhargava et al., 2018 | 19.34 MB | Adobe PDF | ![]() View/Open |
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