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.
","abstract_html":"<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>","abstract_has_math":false,"creators":["Adams, Beau"],"institution":null,"degree_name":"Master of Science","degree_level":"Thesis","degree_discipline":"Biology","degree_department":null,"school":null,"contributors":["Dr. Robert Belton"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2018,"date_issued":"2018-11-01T07:00:00Z","date_published":"2018-11-01T07:00:00Z","updated_at":"2026-07-24T03:24:12Z","subjects":["glioblastoma","cd147","treatment","p53","antibody","cancer","Cancer Biology"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://commons.nmu.edu/theses/565","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Dr. Robert Belton"]},{"key":"dc:creator","label":"Author","values":["Adams, Beau"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2019-03-14T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["glioblastoma","cd147","treatment","p53","antibody","cancer","Cancer Biology"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://commons.nmu.edu/theses/565"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["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.
"]},{"key":"dc:title","label":"Title","values":["CD147 AS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA TREATMENT"]}]}],"canonical_facts":{"dc:contributor":["Dr. Robert Belton"],"dc:creator":["Adams, Beau"],"dc:date.available":["2019-03-14T07:00:00Z"],"dc:description.abstract":["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.
"],"dc:identifier":["https://commons.nmu.edu/theses/565"],"dc:subject":["glioblastoma","cd147","treatment","p53","antibody","cancer","Cancer Biology"],"dc:title":["CD147 AS A POTENTIAL THERAPEUTIC TARGET IN GLIOBLASTOMA TREATMENT"],"thesis:degree_discipline":["Biology"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science"]},"updated_at":"2026-07-24T03:24:12Z"}