The high specificity and affinity of antibodies make them attractive for developing drugs to diagnose and treat cancer. The overarching goal of this work is to explore the synthesis and use of antibody-based imaging agents in preclinical models of cancer. This work can be described as two-fold. In the first part, we investigated how the use of a glycans-specific bioconjugation strategy affects Fc gamma RI binding and why it results in improved in vivo performance of immunoconjugates. To do so, we used the clinically relevant positron emission tomography (PET) imaging agent, 89Zr-DFO-pertuzumab, in mouse models of human breast cancer. In the second part, we developed two imaging agents for ovarian cancer, 89Zr-DFO-AR20.5 for PET and ssB43.13-IR800 for near-infrared fluorescence imaging and evaluated their in vivo performance in mouse models of human ovarian cancer. With this body of work, we hope to demonstrate the potential of antibodies as effective imaging agents for cancer.
","abstract_html":"<p>The high specificity and affinity of antibodies make them attractive for developing drugs to diagnose and treat cancer. The overarching goal of this work is to explore the synthesis and use of antibody-based imaging agents in preclinical models of cancer. This work can be described as two-fold. In the first part, we investigated how the use of a glycans-specific bioconjugation strategy affects Fc gamma RI binding and why it results in improved <em>in vivo </em>performance of immunoconjugates. To do so, we used the clinically relevant positron emission tomography (PET) imaging agent, <sup>89</sup>Zr-DFO-pertuzumab, in mouse models of human breast cancer. In the second part, we developed two imaging agents for ovarian cancer, <sup>89</sup>Zr-DFO-AR20.5 for PET and <sup>ss</sup>B43.13-IR800 for near-infrared fluorescence imaging and evaluated their <em>in vivo </em>performance in mouse models of human ovarian cancer. With this body of work, we hope to demonstrate the potential of antibodies as effective imaging agents for cancer.</p>","abstract_has_math":false,"creators":["Fung, Kimberly C"],"institution":"The Graduate School and University Center of The City University of New York","degree_name":"Doctor of Philosophy","degree_level":"Doctoral","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":["Brian M. Zeglis"],"committee_chairs":[],"committee_members":["Lynn C. Francesconi","Donna McGregor"],"year":2020,"date_issued":"2020-02-01T08:00:00Z","date_published":"2020-02-01T08:00:00Z","updated_at":"2026-07-24T01:58:57Z","subjects":["Biochemistry","Chemistry","Radiochemistry","Positron emission tomography","near-infrared fluorescence Imaging","click chemistry","bioconjugation","cancer"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://academicworks.cuny.edu/gc_etds/3566","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Brian M. Zeglis"]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Lynn C. Francesconi","Donna McGregor"]},{"key":"dc:creator","label":"Author","values":["Fung, Kimberly C"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2020-07-20T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Doctoral"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["The Graduate School and University Center of The City University of New York"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biochemistry","Chemistry","Radiochemistry","Positron emission tomography","near-infrared fluorescence Imaging","click chemistry","bioconjugation","cancer"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://academicworks.cuny.edu/gc_etds/3566"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The high specificity and affinity of antibodies make them attractive for developing drugs to diagnose and treat cancer. The overarching goal of this work is to explore the synthesis and use of antibody-based imaging agents in preclinical models of cancer. This work can be described as two-fold. In the first part, we investigated how the use of a glycans-specific bioconjugation strategy affects Fc gamma RI binding and why it results in improved in vivo performance of immunoconjugates. To do so, we used the clinically relevant positron emission tomography (PET) imaging agent, 89Zr-DFO-pertuzumab, in mouse models of human breast cancer. In the second part, we developed two imaging agents for ovarian cancer, 89Zr-DFO-AR20.5 for PET and ssB43.13-IR800 for near-infrared fluorescence imaging and evaluated their in vivo performance in mouse models of human ovarian cancer. With this body of work, we hope to demonstrate the potential of antibodies as effective imaging agents for cancer.
"]},{"key":"dc:title","label":"Title","values":["Leveraging Antibodies for Positron Emission Tomography and Near-Infrared Fluorescence Imaging of Cancer"]}]}],"canonical_facts":{"dc:contributor.advisor":["Brian M. Zeglis"],"dc:contributor.committeemember":["Lynn C. Francesconi","Donna McGregor"],"dc:creator":["Fung, Kimberly C"],"dc:date.available":["2020-07-20T07:00:00Z"],"dc:description.abstract":["The high specificity and affinity of antibodies make them attractive for developing drugs to diagnose and treat cancer. The overarching goal of this work is to explore the synthesis and use of antibody-based imaging agents in preclinical models of cancer. This work can be described as two-fold. In the first part, we investigated how the use of a glycans-specific bioconjugation strategy affects Fc gamma RI binding and why it results in improved in vivo performance of immunoconjugates. To do so, we used the clinically relevant positron emission tomography (PET) imaging agent, 89Zr-DFO-pertuzumab, in mouse models of human breast cancer. In the second part, we developed two imaging agents for ovarian cancer, 89Zr-DFO-AR20.5 for PET and ssB43.13-IR800 for near-infrared fluorescence imaging and evaluated their in vivo performance in mouse models of human ovarian cancer. With this body of work, we hope to demonstrate the potential of antibodies as effective imaging agents for cancer.
"],"dc:identifier":["https://academicworks.cuny.edu/gc_etds/3566"],"dc:subject":["Biochemistry","Chemistry","Radiochemistry","Positron emission tomography","near-infrared fluorescence Imaging","click chemistry","bioconjugation","cancer"],"dc:title":["Leveraging Antibodies for Positron Emission Tomography and Near-Infrared Fluorescence Imaging of Cancer"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Doctoral"],"thesis:degree_name":["Doctor of Philosophy"],"thesis:institution_name":["The Graduate School and University Center of The City University of New York"]},"updated_at":"2026-07-24T01:58:57Z"}