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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/13807
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dc.contributor.authorChowdhury, Rajdeep-
dc.contributor.authorRoy, Aniruddha-
dc.date.accessioned2024-01-11T06:31:28Z-
dc.date.available2024-01-11T06:31:28Z-
dc.date.issued2020-07-
dc.identifier.urihttps://link.springer.com/article/10.1007/s43440-020-00122-1-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13807-
dc.description.abstractRecent studies have demonstrated that autophagy plays a critical role in reducing the drug sensitivity of docetaxel (DTX) therapy. Disulfiram (DSF) has exhibited potent autophagy inducing activity in multiple studies. We hypothesized that DSF co-treatment could sensitize breast cancer cells to DTX therapy via autophagy modulation.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectPharmacyen_US
dc.subjectDisulfiramen_US
dc.subjectBreast canceren_US
dc.subjectAutophagyen_US
dc.titleDisulfiram potentiates docetaxel cytotoxicity in breast cancer cells through enhanced ROS and autophagyen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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