A review on potential of PARP inhibitors in the treatment of prostate cancer

dc.contributor.advisorSharmin, Shahana
dc.contributor.authorIslam, Saidul
dc.date.accessioned2022-09-26T06:17:43Z
dc.date.available2022-09-26T06:17:43Z
dc.date.issued2022-05
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 33-39).
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.
dc.description.abstractProstate cancer is still a fatal disease at metastatic castration resistance stage (mCRPC) in spite of pursuing advancements in patient survival, indicating the necessity of therapeutic approaches. A significant number of individuals having advanced prostate cancer, most of whom have a poor prognosis, have germinal and/or somatic mutations in their DNA damage response genes. These kinds of mutations lead to a reliance on the Poly (adenosine diphosphate ribose) polymerase for repairing single-strand breaks, indicating the necessity of Poly ADP Ribose Polymerase (PARP) inhibitors. Olaparib was the first FDA approved PARP inhibitor to demonstrate the improved overall survival in mCRPC patients having homologous recombination repair defects. Despite the fact that this is a significant step forward, there are still a number of questions regarding PARP inhibitors. This paper aims to discuss the significance and efficacy of PARP inhibitors mentioning the associated challenges and their future in the treatment of prostate cancer.
dc.identifier.otherID 18146010
dc.identifier.otherhttps://dspace.bracu.ac.bd/server/api/core/items/26aff7c8-f418-4198-b9dd-dbf7e85c1643
dc.identifier.urihttp://hdl.handle.net/10361/17308
dc.language.isoen
dc.publisherBRAC University
dc.sourceBRAC University Institutional Repository
dc.subjectProstate cancer
dc.subjectTherapeutic approaches
dc.subjectmCRPC
dc.subjectPARP inhibitors
dc.subjectOlaparib
dc.titleA review on potential of PARP inhibitors in the treatment of prostate cancer
dc.typeThesis

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