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A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer
Prostate cancer (PCa) is the most commonly diagnosed malignancy and the second leading cause of cancer related death in men. The early diagnosis and treatment of PCa are still challenging due to the lack of efficient tumor targeting agents in traditional managements. Prostate specific membrane antig...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312325/ https://www.ncbi.nlm.nih.gov/pubmed/27448970 http://dx.doi.org/10.18632/oncotarget.10697 |
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author | Han, Donghui Wu, Jieheng Han, Yueheng Wei, Ming Han, Sen Lin, Ruihe Sun, Ziyong Yang, Fa Jiao, Dian Xie, Pin Zhang, Lingling Yang, An-Gang Zhao, Aizhi Wen, Weihong Qin, Weijun |
author_facet | Han, Donghui Wu, Jieheng Han, Yueheng Wei, Ming Han, Sen Lin, Ruihe Sun, Ziyong Yang, Fa Jiao, Dian Xie, Pin Zhang, Lingling Yang, An-Gang Zhao, Aizhi Wen, Weihong Qin, Weijun |
author_sort | Han, Donghui |
collection | PubMed |
description | Prostate cancer (PCa) is the most commonly diagnosed malignancy and the second leading cause of cancer related death in men. The early diagnosis and treatment of PCa are still challenging due to the lack of efficient tumor targeting agents in traditional managements. Prostate specific membrane antigen (PSMA) is highly expressed in PCa, while only has limited expression in other organs, providing an ideal target for the diagnosis and therapy of PCa. The antibody library technique has opened the avenue for the discovery of novel antibodies to be used in the diagnosis and therapy of cancer. In this paper, by screening a large yeast display naive human single chain antibody fragment (scFv) library, we obtained a high affinity scFv targeting PSMA, called gy1. The gy1 scFv was expressed in E.coli and purified via a C terminal 6His tag. The binding affinity of gy1 was shown to be at the nanomolar level and gy1 can specifically bind with PSMA positive cancer cells, and binding triggers its rapid internalization through the endosome-lysosome pathway. The specific targeting of gy1 to PSMA positive tumor tissues was also evaluated in vivo. We showed that the IRDye800CW labeled gy1 can efficiently target and specifically distribute in PSMA positive tumor tissues after being injected into xenograft nude mice. This study indicated that the novel antibody gy1 could be used as a great tool for the development of PSMA targeted imaging and therapy agents for PCa. |
format | Online Article Text |
id | pubmed-5312325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53123252017-03-06 A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer Han, Donghui Wu, Jieheng Han, Yueheng Wei, Ming Han, Sen Lin, Ruihe Sun, Ziyong Yang, Fa Jiao, Dian Xie, Pin Zhang, Lingling Yang, An-Gang Zhao, Aizhi Wen, Weihong Qin, Weijun Oncotarget Research Paper Prostate cancer (PCa) is the most commonly diagnosed malignancy and the second leading cause of cancer related death in men. The early diagnosis and treatment of PCa are still challenging due to the lack of efficient tumor targeting agents in traditional managements. Prostate specific membrane antigen (PSMA) is highly expressed in PCa, while only has limited expression in other organs, providing an ideal target for the diagnosis and therapy of PCa. The antibody library technique has opened the avenue for the discovery of novel antibodies to be used in the diagnosis and therapy of cancer. In this paper, by screening a large yeast display naive human single chain antibody fragment (scFv) library, we obtained a high affinity scFv targeting PSMA, called gy1. The gy1 scFv was expressed in E.coli and purified via a C terminal 6His tag. The binding affinity of gy1 was shown to be at the nanomolar level and gy1 can specifically bind with PSMA positive cancer cells, and binding triggers its rapid internalization through the endosome-lysosome pathway. The specific targeting of gy1 to PSMA positive tumor tissues was also evaluated in vivo. We showed that the IRDye800CW labeled gy1 can efficiently target and specifically distribute in PSMA positive tumor tissues after being injected into xenograft nude mice. This study indicated that the novel antibody gy1 could be used as a great tool for the development of PSMA targeted imaging and therapy agents for PCa. Impact Journals LLC 2016-07-19 /pmc/articles/PMC5312325/ /pubmed/27448970 http://dx.doi.org/10.18632/oncotarget.10697 Text en Copyright: © 2016 Han et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Han, Donghui Wu, Jieheng Han, Yueheng Wei, Ming Han, Sen Lin, Ruihe Sun, Ziyong Yang, Fa Jiao, Dian Xie, Pin Zhang, Lingling Yang, An-Gang Zhao, Aizhi Wen, Weihong Qin, Weijun A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title | A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title_full | A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title_fullStr | A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title_full_unstemmed | A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title_short | A novel anti-PSMA human scFv has the potential to be used as a diagnostic tool in prostate cancer |
title_sort | novel anti-psma human scfv has the potential to be used as a diagnostic tool in prostate cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312325/ https://www.ncbi.nlm.nih.gov/pubmed/27448970 http://dx.doi.org/10.18632/oncotarget.10697 |
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