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Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX
Theranostics is the integration of diagnostic information with pharmaceuticals to increase effectiveness and safety of cancer treatments. Nuclear medicine provides a non-invasive means to visualize drug target expression across primary and metastatic sites, and assess pharmacokinetics and efficacy o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695016/ https://www.ncbi.nlm.nih.gov/pubmed/29158829 http://dx.doi.org/10.7150/thno.21848 |
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author | Lau, Joseph Lin, Kuo-Shyan Bénard, François |
author_facet | Lau, Joseph Lin, Kuo-Shyan Bénard, François |
author_sort | Lau, Joseph |
collection | PubMed |
description | Theranostics is the integration of diagnostic information with pharmaceuticals to increase effectiveness and safety of cancer treatments. Nuclear medicine provides a non-invasive means to visualize drug target expression across primary and metastatic sites, and assess pharmacokinetics and efficacy of companion therapeutic agents. This is significant given the increasing recognition of the importance of clonal heterogeneity in treatment response and resistance. Carbonic anhydrase IX (CA-IX) has been advocated as an attractive diagnostic and therapeutic biomarker for targeting hypoxia in solid malignancies. CA-IX confers cancer cell survival under low oxygen tension, and is associated with increased propensity for metastasis. As such, CA-IX is overexpressed in a broad spectrum of cancers. Different classes of antigen recognition molecules targeting CA-IX including monoclonal antibodies, peptides, small molecule inhibitors, and antibody mimetics have been radiolabeled for imaging and therapeutic applications. cG250, a chimeric monoclonal antibody, has been labeled with an assortment of radionuclides ((124)I, (111)In, (89)Zr, (131)I, (90)Y, and (177)Lu) and is the most extensively investigated CA-IX radiopharmaceutical. In recent years, there have been tremendous advancements made by the research community in developing alternatives to cG250. Although still in preclinical settings, several small molecule inhibitors and antibody mimetics hold great promise in improving the management of aggressive and resistant cancers. |
format | Online Article Text |
id | pubmed-5695016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-56950162017-11-20 Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX Lau, Joseph Lin, Kuo-Shyan Bénard, François Theranostics Review Theranostics is the integration of diagnostic information with pharmaceuticals to increase effectiveness and safety of cancer treatments. Nuclear medicine provides a non-invasive means to visualize drug target expression across primary and metastatic sites, and assess pharmacokinetics and efficacy of companion therapeutic agents. This is significant given the increasing recognition of the importance of clonal heterogeneity in treatment response and resistance. Carbonic anhydrase IX (CA-IX) has been advocated as an attractive diagnostic and therapeutic biomarker for targeting hypoxia in solid malignancies. CA-IX confers cancer cell survival under low oxygen tension, and is associated with increased propensity for metastasis. As such, CA-IX is overexpressed in a broad spectrum of cancers. Different classes of antigen recognition molecules targeting CA-IX including monoclonal antibodies, peptides, small molecule inhibitors, and antibody mimetics have been radiolabeled for imaging and therapeutic applications. cG250, a chimeric monoclonal antibody, has been labeled with an assortment of radionuclides ((124)I, (111)In, (89)Zr, (131)I, (90)Y, and (177)Lu) and is the most extensively investigated CA-IX radiopharmaceutical. In recent years, there have been tremendous advancements made by the research community in developing alternatives to cG250. Although still in preclinical settings, several small molecule inhibitors and antibody mimetics hold great promise in improving the management of aggressive and resistant cancers. Ivyspring International Publisher 2017-09-26 /pmc/articles/PMC5695016/ /pubmed/29158829 http://dx.doi.org/10.7150/thno.21848 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Lau, Joseph Lin, Kuo-Shyan Bénard, François Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title | Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title_full | Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title_fullStr | Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title_full_unstemmed | Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title_short | Past, Present, and Future: Development of Theranostic Agents Targeting Carbonic Anhydrase IX |
title_sort | past, present, and future: development of theranostic agents targeting carbonic anhydrase ix |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695016/ https://www.ncbi.nlm.nih.gov/pubmed/29158829 http://dx.doi.org/10.7150/thno.21848 |
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