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dc.contributor.advisorChowdhury, Namara Mariam
dc.contributor.authorJahan, Nusrat
dc.date.accessioned2024-01-02T10:27:12Z
dc.date.available2024-01-02T10:27:12Z
dc.date.copyright2023
dc.date.issued2023-02
dc.identifier.otherID 19146057
dc.identifier.urihttp://hdl.handle.net/10361/22051
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2023.en_US
dc.descriptionCataloged from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 45-48).
dc.description.abstractCancer is one of the most feared diseases whose prevalence has been drastically increasing in recent years. Among different types of treatment options, the development of kinase-targeted cancer therapies is currently the most studied target for potential anti-cancer therapies. After G-protein-coupled receptors, protein kinases significantly grab the attraction as a target of developing anti-cancer drugs. Based on current research, this review article outlines receptor-interacting protein kinases specially RIP1 and RIP3 as attractive targets over other kinases in the treatment of numerous types of cancer, especially for their tumorigenesis functions in cancer metastasis.en_US
dc.description.statementofresponsibilityNusrat Jahan
dc.format.extent48 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectCanceren_US
dc.subjectRIPKen_US
dc.subjectPathwayen_US
dc.subjectInhibitorsen_US
dc.subjectTherapyen_US
dc.subjectAnti-cancer drugsen_US
dc.subject.lcshCancer--Treatment
dc.titleRIPK pathway, as a potential target, for cancer treatment - a reviewen_US
dc.typeThesisen_US
dc.contributor.departmentSchool of Pharmacy, Brac University
dc.description.degreeB. Pharmacy


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