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A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect
The successful translation of cytotoxic T lymphocyte antigen-4 (CTLA-4) blockade has revolutionized the concept of cancer immunotherapy. Although monoclonal antibody therapeutics remain the mainstream in clinical practice, aptamers are synthetic oligonucleotides that encompass antibody-mimicking fun...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573796/ https://www.ncbi.nlm.nih.gov/pubmed/28918052 http://dx.doi.org/10.1016/j.omtn.2017.08.006 |
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author | Huang, Bo-Tsang Lai, Wei-Yun Chang, Yi-Chung Wang, Jen-Wei Yeh, Shauh-Der Lin, Emily Pei-Ying Yang, Pan-Chyr |
author_facet | Huang, Bo-Tsang Lai, Wei-Yun Chang, Yi-Chung Wang, Jen-Wei Yeh, Shauh-Der Lin, Emily Pei-Ying Yang, Pan-Chyr |
author_sort | Huang, Bo-Tsang |
collection | PubMed |
description | The successful translation of cytotoxic T lymphocyte antigen-4 (CTLA-4) blockade has revolutionized the concept of cancer immunotherapy. Although monoclonal antibody therapeutics remain the mainstream in clinical practice, aptamers are synthetic oligonucleotides that encompass antibody-mimicking functions. Here, we report a novel high-affinity CTLA-4-antagonizing DNA aptamer (dissociation constant, 11.84 nM), aptCTLA-4, which was identified by cell-based SELEX and high-throughput sequencing. aptCTLA-4 is relatively stable in serum, promotes lymphocyte proliferation, and inhibits tumor growth in cell and animal models. Our study demonstrates the developmental pipeline of a functional CTLA-4-targeting aptamer and suggests a translational potential for aptCTLA-4. |
format | Online Article Text |
id | pubmed-5573796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-55737962017-09-05 A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect Huang, Bo-Tsang Lai, Wei-Yun Chang, Yi-Chung Wang, Jen-Wei Yeh, Shauh-Der Lin, Emily Pei-Ying Yang, Pan-Chyr Mol Ther Nucleic Acids Original Article The successful translation of cytotoxic T lymphocyte antigen-4 (CTLA-4) blockade has revolutionized the concept of cancer immunotherapy. Although monoclonal antibody therapeutics remain the mainstream in clinical practice, aptamers are synthetic oligonucleotides that encompass antibody-mimicking functions. Here, we report a novel high-affinity CTLA-4-antagonizing DNA aptamer (dissociation constant, 11.84 nM), aptCTLA-4, which was identified by cell-based SELEX and high-throughput sequencing. aptCTLA-4 is relatively stable in serum, promotes lymphocyte proliferation, and inhibits tumor growth in cell and animal models. Our study demonstrates the developmental pipeline of a functional CTLA-4-targeting aptamer and suggests a translational potential for aptCTLA-4. American Society of Gene & Cell Therapy 2017-08-15 /pmc/articles/PMC5573796/ /pubmed/28918052 http://dx.doi.org/10.1016/j.omtn.2017.08.006 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Huang, Bo-Tsang Lai, Wei-Yun Chang, Yi-Chung Wang, Jen-Wei Yeh, Shauh-Der Lin, Emily Pei-Ying Yang, Pan-Chyr A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title | A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title_full | A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title_fullStr | A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title_full_unstemmed | A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title_short | A CTLA-4 Antagonizing DNA Aptamer with Antitumor Effect |
title_sort | ctla-4 antagonizing dna aptamer with antitumor effect |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573796/ https://www.ncbi.nlm.nih.gov/pubmed/28918052 http://dx.doi.org/10.1016/j.omtn.2017.08.006 |
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