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Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth
ID4, a helix loop helix transcriptional regulator has emerged as a tumor suppressor in prostate cancer. Epigenetic silencing of ID4 promotes prostate cancer whereas ectopic expression in prostate cancer cell lines blocks cancer phenotype. To directly investigate the anti-tumor property, full length...
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/PMC5340093/ https://www.ncbi.nlm.nih.gov/pubmed/27487149 http://dx.doi.org/10.18632/oncotarget.10953 |
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author | Korang-Yeboah, Maxwell Patel, Divya Morton, Derrick Sharma, Pankaj Gorantla, Yamini Joshi, Jugal Nagappan, Perri Pallaniappan, Ravi Chaudhary, Jaideep |
author_facet | Korang-Yeboah, Maxwell Patel, Divya Morton, Derrick Sharma, Pankaj Gorantla, Yamini Joshi, Jugal Nagappan, Perri Pallaniappan, Ravi Chaudhary, Jaideep |
author_sort | Korang-Yeboah, Maxwell |
collection | PubMed |
description | ID4, a helix loop helix transcriptional regulator has emerged as a tumor suppressor in prostate cancer. Epigenetic silencing of ID4 promotes prostate cancer whereas ectopic expression in prostate cancer cell lines blocks cancer phenotype. To directly investigate the anti-tumor property, full length human recombinant ID4 encapsulated in biodegradable Polycaprolactone/Maltodextrin (PCL-MD) nano-carrier was delivered to LNCaP cells in which the native ID4 was stably silenced (LNCaP(-)ID4). The cellular uptake of ID4 resulted in increased apoptosis, decreased proliferation and colony formation. Intratumoral delivery of PCL-MD ID4 into growing LNCaP(-)ID4 tumors in SCID mice significantly reduced the tumor volume compared to the tumors treated with chemotherapeutic Docetaxel. The study supports the feasibility of using nano-carrier encapsulated ID4 protein as a therapeutic. Mechanistically, ID4 may assimilate multiple regulatory pathways for example epigenetic re-programming, integration of multiple AR co-regulators or signaling pathways resulting in tumor suppressor activity of ID4. |
format | Online Article Text |
id | pubmed-5340093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53400932017-03-08 Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth Korang-Yeboah, Maxwell Patel, Divya Morton, Derrick Sharma, Pankaj Gorantla, Yamini Joshi, Jugal Nagappan, Perri Pallaniappan, Ravi Chaudhary, Jaideep Oncotarget Research Paper ID4, a helix loop helix transcriptional regulator has emerged as a tumor suppressor in prostate cancer. Epigenetic silencing of ID4 promotes prostate cancer whereas ectopic expression in prostate cancer cell lines blocks cancer phenotype. To directly investigate the anti-tumor property, full length human recombinant ID4 encapsulated in biodegradable Polycaprolactone/Maltodextrin (PCL-MD) nano-carrier was delivered to LNCaP cells in which the native ID4 was stably silenced (LNCaP(-)ID4). The cellular uptake of ID4 resulted in increased apoptosis, decreased proliferation and colony formation. Intratumoral delivery of PCL-MD ID4 into growing LNCaP(-)ID4 tumors in SCID mice significantly reduced the tumor volume compared to the tumors treated with chemotherapeutic Docetaxel. The study supports the feasibility of using nano-carrier encapsulated ID4 protein as a therapeutic. Mechanistically, ID4 may assimilate multiple regulatory pathways for example epigenetic re-programming, integration of multiple AR co-regulators or signaling pathways resulting in tumor suppressor activity of ID4. Impact Journals LLC 2016-07-30 /pmc/articles/PMC5340093/ /pubmed/27487149 http://dx.doi.org/10.18632/oncotarget.10953 Text en Copyright: © 2016 Korang-Yeboah et al. http://creativecommons.org/licenses/by/3.0/ 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 Korang-Yeboah, Maxwell Patel, Divya Morton, Derrick Sharma, Pankaj Gorantla, Yamini Joshi, Jugal Nagappan, Perri Pallaniappan, Ravi Chaudhary, Jaideep Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title | Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title_full | Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title_fullStr | Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title_full_unstemmed | Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title_short | Intra-tumoral delivery of functional ID4 protein via PCL/maltodextrin nano-particle inhibits prostate cancer growth |
title_sort | intra-tumoral delivery of functional id4 protein via pcl/maltodextrin nano-particle inhibits prostate cancer growth |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340093/ https://www.ncbi.nlm.nih.gov/pubmed/27487149 http://dx.doi.org/10.18632/oncotarget.10953 |
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