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Bijesh K. Biswal

Researcher at National Institute of Technology, Rourkela

Publications -  32
Citations -  573

Bijesh K. Biswal is an academic researcher from National Institute of Technology, Rourkela. The author has contributed to research in topics: Cancer & Lung cancer. The author has an hindex of 10, co-authored 27 publications receiving 309 citations. Previous affiliations of Bijesh K. Biswal include Indian Institute of Technology Madras & Dartmouth College.

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Emerging role of plumbagin: Cytotoxic potential and pharmaceutical relevance towards cancer therapy.

TL;DR: Nano encapsulation of plumbagin overcomes the poor water solubility and bioavailability obstacles, enhancing the pharmaceutical relevance with better therapeutic efficacy and can be introduced as a future phytotherapeutic anticancer drug after fully satisfied preclinical and clinical trials.
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Cell signaling and cancer: a mechanistic insight into drug resistance

TL;DR: This review outlines the different mechanisms enabling resistance including drug efflux, drug target alternation, alternative splicing, the release of the extracellular vesicle, tumor heterogeneity, epithelial-mesenchymal transition, tumor microenvironment, and the secondary mutation in the receptor.
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Piperlongumine, a potent anticancer phytotherapeutic: Perspectives on contemporary status and future possibilities as an anticancer agent

TL;DR: Piperlongumine, a white to beige biologically active alkaloid/amide phytochemical, has high pharmacological relevance as an anticancer agent in both preclinical and clinical settings as discussed by the authors.
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Acute hypersensitivity of pluripotent testicular cancer-derived embryonal carcinoma to low-dose 5-aza deoxycytidine is associated with global DNA Damage-associated p53 activation, anti-pluripotency and DNA demethylation.

TL;DR: It is shown here that low-dose 5-aza treatment results in DNA damage and induction of p53 in NT2/D1 cells and results in global and gene specific promoter DNA hypomethylation in p53 and pluripotency genes.
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Development of a targeted siRNA delivery system using FOL-PEG-PEI conjugate.

TL;DR: This study has shown that receptor mediated delivery of siRNA enables silencing of target genes in specific tissues and can be extended to deliver a wide range of drugs and post-transcriptional gene silencing therapeutics.