{"id":{"repo_id":"texas-state","oai_identifier":"oai:digital.library.txst.edu:10877/4331"},"canonical_url":"https://search.dev.ndltd.org/etd/texas-state/oai:digital.library.txst.edu:10877/4331","repository":{"repo_id":"texas-state","name":"Texas State University","base_url":"https://digital.library.txst.edu/server/oai/request"},"display":{"title":"Aptamer Interactions and Applications in Cancer Treatment","abstract":"Aptamers, small strands of RNA or DNA, are finding a rapidly expanding repertoire of applications. Aptamers have found numerous diagnostic and therapeutic uses both in vitro and in vivo. Specifically, their application in diagnosis and treatment of multiple cancers has been strongly advanced over the last decade. In this study, two different applications of aptamers are explored for two different cancers. In the murine liver cancer cell line, BNL 1ME A.7R.1 (MEAR), the TLS-11a aptamer is shown to quickly internalize at physiological temperatures. The TLS-11a aptamer is therefore a potential candidate for intracellular toxin delivery as a means of inducing targeted apoptosis of the MEAR cancer cells. In the human breast cancer cell line MCF7, the MUC1-5TR aptamer is shown to successfully initiate the classical complement pathway leading to complement fixation on the target cell via a streptavidin-C1q conjugation. This model provides a way to help the human immune system specifically target and remove cancerous cells.","abstract_html":"Aptamers, small strands of RNA or DNA, are finding a rapidly expanding repertoire of applications. Aptamers have found numerous diagnostic and therapeutic uses both in vitro and in vivo. Specifically, their application in diagnosis and treatment of multiple cancers has been strongly advanced over the last decade. In this study, two different applications of aptamers are explored for two different cancers. In the murine liver cancer cell line, BNL 1ME A.7R.1 (MEAR), the TLS-11a aptamer is shown to quickly internalize at physiological temperatures. The TLS-11a aptamer is therefore a potential candidate for intracellular toxin delivery as a means of inducing targeted apoptosis of the MEAR cancer cells. In the human breast cancer cell line MCF7, the MUC1-5TR aptamer is shown to successfully initiate the classical complement pathway leading to complement fixation on the target cell via a streptavidin-C1q conjugation. This model provides a way to help the human immune system specifically target and remove cancerous cells.","abstract_has_math":false,"creators":["Stecker, John"],"institution":"Texas State University","degree_name":"Master of Science","degree_level":"Masters","degree_discipline":"Biology","degree_department":null,"school":null,"contributors":[],"advisors":["Koke, Joseph R."],"committee_chairs":[],"committee_members":["Garcia, Dana M.","Bruno, John G."],"year":2011,"date_issued":"2011-12","date_published":"2011-12","updated_at":"2026-07-27T21:22:35Z","subjects":["cancer","aptamers","cancer treatments"],"languages":["en"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/10877/4331","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Koke, Joseph R."]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Garcia, Dana M.","Bruno, John G."]},{"key":"dc:creator","label":"Author","values":["Stecker, John"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2012-08-15T19:26:40Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2012-08-15T19:26:40Z"]},{"key":"dc:date.issued","label":"Date","values":["2011-12"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Texas State University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["cancer","aptamers","cancer treatments"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/10877/4331"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Aptamers, small strands of RNA or DNA, are finding a rapidly expanding repertoire of applications. 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In this study, two different applications of aptamers are explored for two different cancers. In the murine liver cancer cell line, BNL 1ME A.7R.1 (MEAR), the TLS-11a aptamer is shown to quickly internalize at physiological temperatures. The TLS-11a aptamer is therefore a potential candidate for intracellular toxin delivery as a means of inducing targeted apoptosis of the MEAR cancer cells. In the human breast cancer cell line MCF7, the MUC1-5TR aptamer is shown to successfully initiate the classical complement pathway leading to complement fixation on the target cell via a streptavidin-C1q conjugation. 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