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Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection
We described the selection of a novel nucleic acid antibody-like prostate cancer (PCa) that specifically binds to the single-stranded DNA molecule from a 277-nt fragment that may have been partially paired and bound to the PCA3 RNA conformational structure. PCA3-277 aptamer ligands were obtained, an...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502603/ https://www.ncbi.nlm.nih.gov/pubmed/26174796 http://dx.doi.org/10.1038/srep12090 |
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author | Marangoni, Karina Neves, Adriana F. Rocha, Rafael M. Faria, Paulo R. Alves, Patrícia T. Souza, Aline G. Fujimura, Patrícia T. Santos, Fabiana A. A. Araújo, Thaise G. Ward, Laura S. Goulart, Luiz R. |
author_facet | Marangoni, Karina Neves, Adriana F. Rocha, Rafael M. Faria, Paulo R. Alves, Patrícia T. Souza, Aline G. Fujimura, Patrícia T. Santos, Fabiana A. A. Araújo, Thaise G. Ward, Laura S. Goulart, Luiz R. |
author_sort | Marangoni, Karina |
collection | PubMed |
description | We described the selection of a novel nucleic acid antibody-like prostate cancer (PCa) that specifically binds to the single-stranded DNA molecule from a 277-nt fragment that may have been partially paired and bound to the PCA3 RNA conformational structure. PCA3-277 aptamer ligands were obtained, and the best binding molecule, named CG3, was synthesized for validation. Aiming to prove its diagnostic utility, we used an apta-qPCR assay with CG3-aptamer conjugated to magnetic beads to capture PCA3 transcripts, which were amplified 97-fold and 7-fold higher than conventional qPCR in blood and tissue, respectively. Histopathologic analysis of 161 prostate biopsies arranged in a TMA and marked with biotin-labeled CG3-aptamer showed moderate staining in both cytoplasm and nucleus of PCa samples; in contrast, benign prostatic hyperplasia (BPH) samples presented strong nuclear staining (78% of the cases). No staining was observed in stromal cells. In addition, using an apta-qPCR, we demonstrated that CG3-aptamer specifically recognizes the conformational PCA3-277 molecule and at least three other transcript variants, indicating that long non-coding RNA (lncRNA) is processed after transcription. We suggest that CG3-aptamer may be a useful PCa diagnostic tool. In addition, this molecule may be used in drug design and drug delivery for PCa therapy. |
format | Online Article Text |
id | pubmed-4502603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45026032015-07-17 Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection Marangoni, Karina Neves, Adriana F. Rocha, Rafael M. Faria, Paulo R. Alves, Patrícia T. Souza, Aline G. Fujimura, Patrícia T. Santos, Fabiana A. A. Araújo, Thaise G. Ward, Laura S. Goulart, Luiz R. Sci Rep Article We described the selection of a novel nucleic acid antibody-like prostate cancer (PCa) that specifically binds to the single-stranded DNA molecule from a 277-nt fragment that may have been partially paired and bound to the PCA3 RNA conformational structure. PCA3-277 aptamer ligands were obtained, and the best binding molecule, named CG3, was synthesized for validation. Aiming to prove its diagnostic utility, we used an apta-qPCR assay with CG3-aptamer conjugated to magnetic beads to capture PCA3 transcripts, which were amplified 97-fold and 7-fold higher than conventional qPCR in blood and tissue, respectively. Histopathologic analysis of 161 prostate biopsies arranged in a TMA and marked with biotin-labeled CG3-aptamer showed moderate staining in both cytoplasm and nucleus of PCa samples; in contrast, benign prostatic hyperplasia (BPH) samples presented strong nuclear staining (78% of the cases). No staining was observed in stromal cells. In addition, using an apta-qPCR, we demonstrated that CG3-aptamer specifically recognizes the conformational PCA3-277 molecule and at least three other transcript variants, indicating that long non-coding RNA (lncRNA) is processed after transcription. We suggest that CG3-aptamer may be a useful PCa diagnostic tool. In addition, this molecule may be used in drug design and drug delivery for PCa therapy. Nature Publishing Group 2015-07-15 /pmc/articles/PMC4502603/ /pubmed/26174796 http://dx.doi.org/10.1038/srep12090 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Marangoni, Karina Neves, Adriana F. Rocha, Rafael M. Faria, Paulo R. Alves, Patrícia T. Souza, Aline G. Fujimura, Patrícia T. Santos, Fabiana A. A. Araújo, Thaise G. Ward, Laura S. Goulart, Luiz R. Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title | Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title_full | Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title_fullStr | Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title_full_unstemmed | Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title_short | Prostate-specific RNA aptamer: promising nucleic acid antibody-like cancer detection |
title_sort | prostate-specific rna aptamer: promising nucleic acid antibody-like cancer detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502603/ https://www.ncbi.nlm.nih.gov/pubmed/26174796 http://dx.doi.org/10.1038/srep12090 |
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