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• W3146358220 endingPage "111723" @default.
• W3146358220 startingPage "111723" @default.
• W3146358220 abstract "Although the biomedical sciences have achieved tremendous success in developing novel approaches to managing prostate cancer, this disease remains one of the major health concerns among men worldwide. Liposomal formulations of single drugs have shown promising results in cancer treatment; however, the use of multi drugs has shown a better therapeutic index than individual drugs. The identification of cancer-specific receptors has added value to design targeted drug delivering nanocarriers. We have developed genistein and plumbagin co-encapsulating liposomes (∼120 nm) with PSMA specific antibodies to target prostate cancer cells selectively in this work. These liposomes showed >90 % decrease in PSMA expressing prostate cancer cell proliferation without any appreciable toxicity to healthy cells and human red blood cells. Release of plumbagin and genistein was found to decrease the expression of PI3/AKT3 signaling proteins and Glut-1 receptors (inhibited glucose uptake and metabolism), respectively. The decrease in migration potential of cells and induced apoptosis established the observed anti-proliferative effect in prostate cancer cell lines. The discussed strategy of developing novel, non-toxic, and PSMA specific antibody conjugated liposomes carrying genistein and plumbagin drugs may also be used for encapsulating other drugs and inhibit the growth of different types of cancers." @default.
• W3146358220 created "2021-04-13" @default.
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• W3146358220 date "2021-07-01" @default.
• W3146358220 modified "2023-10-10" @default.
• W3146358220 title "PSMA conjugated combinatorial liposomal formulation encapsulating genistein and plumbagin to induce apoptosis in prostate cancer cells" @default.
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• W3146358220 doi "https://doi.org/10.1016/j.colsurfb.2021.111723" @default.
• W3146358220 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33839474" @default.
• W3146358220 hasPublicationYear "2021" @default.
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