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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2141
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dc.contributor.advisor
dc.contributor.advisor
dc.contributor.authorChowdhury, Rajdeep
dc.contributor.authorChowdhury, Shibasish
dc.contributor.author
dc.contributor.authorMukherjee, Sudeshna
dc.date.accessioned2021-09-27T07:47:10Z
dc.date.available2021-09-27T07:47:10Z
dc.date.issued2021-01
dc.identifier.urihttps://cancerci.biomedcentral.com/articles/10.1186/s12935-020-01720-y
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2141
dc.description.abstractOsteosarcoma (OS) is a malignant tumor of the bone mostly observed in children and adolescents. The current treatment approach includes neoadjuvant and adjuvant chemotherapy; however, drug resistance often hinders therapy in OS patients. Also, the post-relapse survival of OS patients is as low as 20%. We therefore planned to understand the molecular cause for its poor prognosis and design an appropriate therapeutic strategy to combat the disease.en_US
dc.language.isoenen_US
dc.publisherSpringer Natureen_US
dc.subjectBiologyen_US
dc.subjectVerteporfinen_US
dc.subjectAutophagyen_US
dc.subjectOsteosarcoma cellsen_US
dc.titleVerteporfin disrupts multiple steps of autophagy and regulates p53 to sensitize osteosarcoma cellsen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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