Welcome to the upgraded BRAC University Institutional Repository. We are currently organizing collections after a recent system upgrade. Homepage category counters may temporarily show lower numbers while syncing, but over 27,000 repository items remain safe and accessible. Please use the search bar to find theses, scholarly outputs, and institutional documents.

A comprehensive bioinformatics analysis of BRAF in cancer

bracu.degree.levelUndergraduate
bracu.type.groupStudent Works
datacite.rightsOpen Access
dc.contributor.advisorHossain, M. Zulfiquer
dc.contributor.authorAhmed, Bagdad
dc.contributor.departmentDepartment of Pharmacy
dc.date.accessioned2021-10-24T08:50:49Z
dc.date.available2021-10-24T08:50:49Z
dc.date.copyright2021
dc.date.issued2021-09
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 39-43).
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2021.en_US
dc.description.abstractBRAF is one of the most vital serine/ threonine-protein kinase proto-oncogenes that performs a crucial role in cellular proliferation, growth, signaling and secretion. By deregulation of this gene can lead to terrible consequences including cancer. By utilizing the available dataset from Genotype-Tissue Expression (GTEx) and the Cancer Genome Atlas database we found that BRAF is overexpressed among 12 cancers. Moreover, BRAF overexpression is common in the late stages of cancers. Thus, we can understand its complicity with cancer invasion and progression. Furthermore, the study divulges a set of cancer that has a short overall survival time (OS) and poor prognosis due to dysregulation of this gene. We found two specific cancers PRAD (Prostate adenocarcinoma) wherein BRAF is overexpressed and KIRC (Kidney Renal Clear Cell Carcinoma) that has BRAF lower expressed. Key nodes for both cancers generated by PPI networks and potential druggability for both concerns were shown. Considering this cancer as a new target and understanding the proper role of BRAF on them by further study can lead to new therapies for both cancers.en_US
dc.description.degreeBachelor of Pharmacy
dc.description.statementofresponsibilityBagdad Ahmed
dc.format.extent43 pages
dc.identifier.otherID 17346015
dc.identifier.urihttp://hdl.handle.net/10361/15526
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.subjectBRAFen_US
dc.subjectTCGAen_US
dc.subjectGTExen_US
dc.subjectCanceren_US
dc.subjectProtein-protein interactionen_US
dc.subjectDruggabilityen_US
dc.subject.lcshCancer--Treatment
dc.titleA comprehensive bioinformatics analysis of BRAF in canceren_US
dc.typeThesisen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
17346015_PHR.pdf
Size:
2.52 MB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: