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dc.contributor.advisorKabir, MD. Tanvir
dc.contributor.authorRaju, Md. Ismail
dc.date.accessioned2022-12-13T03:31:06Z
dc.date.available2022-12-13T03:31:06Z
dc.date.copyright2022
dc.date.issued2022-03
dc.identifier.otherID 17346042
dc.identifier.urihttp://hdl.handle.net/10361/17637
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.en_US
dc.descriptionCataloged from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 54-79).
dc.description.abstractGlioblastoma multiforme is one of the common forms of brain cancer found worldwide, and treatment options are limited for this deadly disease. Various targeted treatments are being investigated, but no breakthroughs have yet been made. One of the most promising aspects of the glioblastoma treatment is the restriction of the intracellular signal transduction,also known asthe strain transformingpathway, and recently it has become the hotspot of brain cancer research. Sorafenib is a model drug that has shown signs of success in preclinical trials. Sorafenib, which is a multi-kinase inhibitor, induces growth arrest and apoptosis of human glioblastoma cells through the dephosphorylation of signal transducers and activators of transcription 3 and thus poses a promising aspect in developing a potential treatment of glioblastoma. This thesis report focuses on the use of sorafenib for the Protein kinase B (AKT) inhibition as a potential cure for glioblastoma.en_US
dc.description.statementofresponsibilityMd. Ismail Raju
dc.format.extent79 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.subjectGlioblastomaen_US
dc.subjectAKT inhibition pathwayen_US
dc.subjectSorafeniben_US
dc.subjectTumor cell proliferationen_US
dc.subjectDephosphorylationen_US
dc.subject.lcshCancer cells
dc.titleArresting tumor cell proliferation and inhibition of AKT pathway via the use of multikinase inhibitor sorafenib forthe treatment of glioblastomaen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Pharmacy, Brac University
dc.description.degreeB. Pharmacy


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