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Northern Michigan University

CD147 AS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA TREATMENT

Abstract

dc:description.abstract

<p>Glioblastoma (GBM) tumors are the most common and lethal form of cancer in the central nervous system (CNS). GBM tumors appear to contain a mixture of different cell types, which makes them difficult to treat. GBM cells exhibit altered morphology from normal cells on several different levels, which highlights different pathways to potentially target for therapeutic treatments. The human surface glycoprotein CD147, also known as basigin, is expressed at significantly higher levels in GBMs compared to non-neoplastic brain tissue. Furthermore, levels of CD147 expression correlate with brain tumor progression and show the highest expression in GBM. Here, we suppressed tumor cell growth using anti-CD147 monoclonal antibodies. An apoptosis/necrosis assay suggests that GBM cells treated with anti-CD147 monoclonal antibodies were not experiencing a form of induced cell death. Rather, our cell proliferation assay results suggest that anti-CD147 monoclonal antibody treated cells had significantly deceased cell proliferation when compared with control cells. Together, these results show that CD147 is a potential therapeutic target for GBM treatment.</p>

Degree

thesis:*
Name thesis:degree_name
Master of Science
Level thesis:degree_level
Thesis
Discipline thesis:degree_discipline
Biology
Year dc:date.available
2018

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Adams, Beau
Contributors dc:contributor
  • Dr. Robert Belton

Subjects

dc:subject × 7

Identifiers

dc:identifier.*
Repository record dc:identifier
https://commons.nmu.edu/theses/565
OAI identifier oai:identifier
oai:commons.nmu.edu:theses-1590

Chain of custody

source
Harvested from
Northern Michigan University
Base URL
commons.nmu.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Adams, Beau. CD147 AS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA TREATMENT. Thesis thesis, 2018. https://commons.nmu.edu/theses/565