Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1541
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dc.contributor.authorDalal, Nishu-
dc.contributor.authorMakharia, Govind K-
dc.contributor.authorDalal, Monu-
dc.contributor.authorMohan, Anand-
dc.contributor.authorSingh, Rajeev-
dc.contributor.authorKumar, Anil-
dc.date.accessioned2025-02-17T06:21:08Z-
dc.date.available2025-02-17T06:21:08Z-
dc.date.issued2023-12-
dc.identifier.urihttp://hdl.handle.net/123456789/1541-
dc.description.abstractThere are a number of reports about anticancer activity of indole derivatives. In this study, we investigated the role of indoxyl sulfate (IS) for its selective anticancer activity on colon cancer cells. IS treatment on HCT-116 and HT-29 human epithelial adenocarcinoma cells led to a decrease in cell proliferation, cell viability, and ATP content. Colon cancer cells showed a 10% increase in cell apoptosis in comparison to control. Due to IS treatment, cell morphology got distorted, cell number found decreased, intracellular vesicles formed, and cells were found floating in the media. Cells also showed a loss in membrane integrity and a decrease in colony-forming ability and ceased at the G2/M phase of the cell cycle. No significant change was noted in the level of inflammatory cytokines IL-17A, IL-1β, and TNF-α, histology, length of intestine, and spleen after 100 mM IS treatment to balb/c mice. These observations indicate the selective anticancer effect of IS on colon cancer cells.en_US
dc.language.isoenen_US
dc.titleGut Metabolite Indoxyl Sulfate Has Selective Deleterious and Anticancer Effect on Colon Cancer Cellsen_US
dc.typeArticleen_US
dc.journalJ Med Chemen_US
dc.volumeno6en_US
dc.issueno(24)en_US
dc.pages17074-17085en_US
Appears in Collections:Genes and Proteins, Publications



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