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Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy
Delivery of imaging reagents and drugs to tumors is essential for cancer diagnosis and therapy. In addition to therapeutic and diagnostic functionalities, peptides have potential benefits such as biocompatibility, ease to synthesize, smaller size, by-passing off-target side effects, and achieving th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324683/ https://www.ncbi.nlm.nih.gov/pubmed/30647857 http://dx.doi.org/10.18632/oncotarget.26442 |
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author | Tripathi, Prem Prakash Arami, Hamed Banga, Ivneet Gupta, Jalaj Gandhi, Sonu |
author_facet | Tripathi, Prem Prakash Arami, Hamed Banga, Ivneet Gupta, Jalaj Gandhi, Sonu |
author_sort | Tripathi, Prem Prakash |
collection | PubMed |
description | Delivery of imaging reagents and drugs to tumors is essential for cancer diagnosis and therapy. In addition to therapeutic and diagnostic functionalities, peptides have potential benefits such as biocompatibility, ease to synthesize, smaller size, by-passing off-target side effects, and achieving the beneficial effects with lower-administered dosages. A particular type of peptide known as cell penetrating peptides (CPP) have been predominantly studied during last twenty years as they are not only capable to translocate themselves across membranes but also allow carrier drugs to translocate across plasma membrane, by different mechanisms depending on the CPP. This is of great potential importance in drug delivery systems, as the ability to pass across membranes is crucial to many drug delivery systems. In spite of significant progress in design and application of CPP, more investigations are required to further improve their delivery to tumors, with reduced side-effect and enhanced therapeutic efficacy. In this review, we emphasis on current advancements in preclinical and clinical trials based on using CPP for more efficient delivery of anti-cancer drugs and imaging reagents to cancer tissues and individual cells associated with them. We discuss the evolution of the CPPs-based strategies for targeted delivery, their current status and strengths, along with summarizing the role of CPPs in targeted drug delivery. We also discuss some recently reported diagnostic applications of engineered protease-responsive substrates and activable imaging complexes. We highlight the recent clinical trial data by providing a road map for better design of the CPPs for future preclinical and clinical applications. |
format | Online Article Text |
id | pubmed-6324683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63246832019-01-15 Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy Tripathi, Prem Prakash Arami, Hamed Banga, Ivneet Gupta, Jalaj Gandhi, Sonu Oncotarget Review Delivery of imaging reagents and drugs to tumors is essential for cancer diagnosis and therapy. In addition to therapeutic and diagnostic functionalities, peptides have potential benefits such as biocompatibility, ease to synthesize, smaller size, by-passing off-target side effects, and achieving the beneficial effects with lower-administered dosages. A particular type of peptide known as cell penetrating peptides (CPP) have been predominantly studied during last twenty years as they are not only capable to translocate themselves across membranes but also allow carrier drugs to translocate across plasma membrane, by different mechanisms depending on the CPP. This is of great potential importance in drug delivery systems, as the ability to pass across membranes is crucial to many drug delivery systems. In spite of significant progress in design and application of CPP, more investigations are required to further improve their delivery to tumors, with reduced side-effect and enhanced therapeutic efficacy. In this review, we emphasis on current advancements in preclinical and clinical trials based on using CPP for more efficient delivery of anti-cancer drugs and imaging reagents to cancer tissues and individual cells associated with them. We discuss the evolution of the CPPs-based strategies for targeted delivery, their current status and strengths, along with summarizing the role of CPPs in targeted drug delivery. We also discuss some recently reported diagnostic applications of engineered protease-responsive substrates and activable imaging complexes. We highlight the recent clinical trial data by providing a road map for better design of the CPPs for future preclinical and clinical applications. Impact Journals LLC 2018-12-14 /pmc/articles/PMC6324683/ /pubmed/30647857 http://dx.doi.org/10.18632/oncotarget.26442 Text en Copyright: © 2018 Tripathi et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Review Tripathi, Prem Prakash Arami, Hamed Banga, Ivneet Gupta, Jalaj Gandhi, Sonu Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title | Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title_full | Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title_fullStr | Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title_full_unstemmed | Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title_short | Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
title_sort | cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324683/ https://www.ncbi.nlm.nih.gov/pubmed/30647857 http://dx.doi.org/10.18632/oncotarget.26442 |
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