dc.contributor.advisor | Haque, Fahim Kabir Monjurul | |
dc.contributor.author | Kenneth, Mutebi John | |
dc.date.accessioned | 2022-02-27T05:37:00Z | |
dc.date.available | 2022-02-27T05:37:00Z | |
dc.date.copyright | 2021 | |
dc.date.issued | 2021-12 | |
dc.identifier.other | ID 20376006 | |
dc.identifier.uri | http://hdl.handle.net/10361/16349 | |
dc.description | This thesis report is submitted in partial fulfillment of the requirement for the degree of Master of Science in Biotechnology, 2021. | en_US |
dc.description | Catalogued from PDF version of thesis. | |
dc.description | Includes bibliographical references (pages 23-31). | |
dc.description.abstract | According to the World Health Organization (WHO) report of 2020, Colorectal Cancer (CRC)
is the third most common type of cancer and the second cause of cancer-related deaths in the
world. However, the existing treatment, as well as prognosis strategies, need to be improved to
increase the survival of CRC patients. Targeted therapies of CRC as opposed to ordinary
therapies; target key biological features and pathways of cancerous cells hence minimizing the
subsequent damage to normal cells. MicroRNAs have been reported to play a crucial role in
inhibiting and/or suppressing major pathways in various cancer types by targeting transcripts
of key genes in such pathways. This study aimed at in silico inhibiting cancer cell proliferation
and metastasis by targeting a key gene – Frizzled receptor 3 (FZD3) in the Wnt signaling
pathway, one of the major pathways in CRC; using microRNAs. The in silico analysis revealed
that miR-98-5p is a direct target of FZD3, using 5 microarray datasets containing tumorous and
control samples. Further analysis indicated that miR-98-5p inhibits the expression of this
receptor by directly binding to the 3’UTR of its mRNA hence exerting a tumor-suppressor role
in CRC through the Wnt signaling pathway. However, these results need to be validated in the
future through basic research experiments using CRC cells in vivo and in vitro. The study
reveals miR-98-5p as a novel target of FZD3 and an inhibitor of the Wnt signaling pathway
hence being a potential candidate for developing targeted therapies against CRC. | en_US |
dc.description.statementofresponsibility | Mutebi John Kenneth | |
dc.format.extent | 31 pages | |
dc.language.iso | en | en_US |
dc.publisher | Brac University | en_US |
dc.rights | Brac 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.subject | Frizzled receptor 3 (FZD3) | en_US |
dc.subject | Colorectal Cancer | en_US |
dc.subject | miR-98-5p | en_US |
dc.subject | Tumor cell | en_US |
dc.subject | Wnt signaling pathway | en_US |
dc.subject.lcsh | Colon (Anatomy) -- Cancer. | |
dc.subject.lcsh | Colorectal Neoplasms. | |
dc.subject.lcsh | Rectum -- Cancer. | |
dc.title | Bioinformatics Analysis Reveals miR-98-5p as a potential Inhibitor of Tumor cell proliferation and metastasis in Colorectal Cancer by targeting the FZD3 receptor of the Wnt signaling pathway | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | Department of Mathematics and Natural Sciences, Brac University | |
dc.description.degree | M. Biotechnology | |