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X-Ray Psoralen Activated Cancer Therapy (X-PACT)
This work investigates X-PACT (X-ray Psoralen Activated Cancer Therapy): a new approach for the treatment of solid cancer. X-PACT utilizes psoralen, a potent anti-cancer therapeutic with current application to proliferative disease and extracorporeal photopheresis (ECP) of cutaneous T Cell Lymphoma....
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008763/ https://www.ncbi.nlm.nih.gov/pubmed/27583569 http://dx.doi.org/10.1371/journal.pone.0162078 |
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author | Oldham, Mark Yoon, Paul Fathi, Zak Beyer, Wayne F. Adamson, Justus Liu, Leihua Alcorta, David Xia, Wenle Osada, Takuya Liu, Congxiao Yang, Xiao Y. Dodd, Rebecca D. Herndon, James E. Meng, Boyu Kirsch, David G. Lyerly, H. Kim Dewhirst, Mark W. Fecci, Peter Walder, Harold Spector, Neil L. |
author_facet | Oldham, Mark Yoon, Paul Fathi, Zak Beyer, Wayne F. Adamson, Justus Liu, Leihua Alcorta, David Xia, Wenle Osada, Takuya Liu, Congxiao Yang, Xiao Y. Dodd, Rebecca D. Herndon, James E. Meng, Boyu Kirsch, David G. Lyerly, H. Kim Dewhirst, Mark W. Fecci, Peter Walder, Harold Spector, Neil L. |
author_sort | Oldham, Mark |
collection | PubMed |
description | This work investigates X-PACT (X-ray Psoralen Activated Cancer Therapy): a new approach for the treatment of solid cancer. X-PACT utilizes psoralen, a potent anti-cancer therapeutic with current application to proliferative disease and extracorporeal photopheresis (ECP) of cutaneous T Cell Lymphoma. An immunogenic role for light-activated psoralen has been reported, contributing to long-term clinical responses. Psoralen therapies have to-date been limited to superficial or extracorporeal scenarios due to the requirement for psoralen activation by UVA light, which has limited penetration in tissue. X-PACT solves this challenge by activating psoralen with UV light emitted from novel non-tethered phosphors (co-incubated with psoralen) that absorb x-rays and re-radiate (phosphoresce) at UV wavelengths. The efficacy of X-PACT was evaluated in both in-vitro and in-vivo settings. In-vitro studies utilized breast (4T1), glioma (CT2A) and sarcoma (KP-B) cell lines. Cells were exposed to X-PACT treatments where the concentrations of drug (psoralen and phosphor) and radiation parameters (energy, dose, and dose rate) were varied. Efficacy was evaluated primarily using flow cell cytometry in combination with complimentary assays, and the in-vivo mouse study. In an in-vitro study, we show that X-PACT induces significant tumor cell apoptosis and cytotoxicity, unlike psoralen or phosphor alone (p<0.0001). We also show that apoptosis increases as doses of phosphor, psoralen, or radiation increase. Finally, in an in-vivo pilot study of BALBc mice with syngeneic 4T1 tumors, we show that the rate of tumor growth is slower with X-PACT than with saline or AMT + X-ray (p<0.0001). Overall these studies demonstrate a potential therapeutic effect for X-PACT, and provide a foundation and rationale for future studies. In summary, X-PACT represents a novel treatment approach in which well-tolerated low doses of x-ray radiation are delivered to a specific tumor site to generate UVA light which in-turn unleashes both short- and potentially long-term antitumor activity of photo-active therapeutics like psoralen. |
format | Online Article Text |
id | pubmed-5008763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50087632016-09-27 X-Ray Psoralen Activated Cancer Therapy (X-PACT) Oldham, Mark Yoon, Paul Fathi, Zak Beyer, Wayne F. Adamson, Justus Liu, Leihua Alcorta, David Xia, Wenle Osada, Takuya Liu, Congxiao Yang, Xiao Y. Dodd, Rebecca D. Herndon, James E. Meng, Boyu Kirsch, David G. Lyerly, H. Kim Dewhirst, Mark W. Fecci, Peter Walder, Harold Spector, Neil L. PLoS One Research Article This work investigates X-PACT (X-ray Psoralen Activated Cancer Therapy): a new approach for the treatment of solid cancer. X-PACT utilizes psoralen, a potent anti-cancer therapeutic with current application to proliferative disease and extracorporeal photopheresis (ECP) of cutaneous T Cell Lymphoma. An immunogenic role for light-activated psoralen has been reported, contributing to long-term clinical responses. Psoralen therapies have to-date been limited to superficial or extracorporeal scenarios due to the requirement for psoralen activation by UVA light, which has limited penetration in tissue. X-PACT solves this challenge by activating psoralen with UV light emitted from novel non-tethered phosphors (co-incubated with psoralen) that absorb x-rays and re-radiate (phosphoresce) at UV wavelengths. The efficacy of X-PACT was evaluated in both in-vitro and in-vivo settings. In-vitro studies utilized breast (4T1), glioma (CT2A) and sarcoma (KP-B) cell lines. Cells were exposed to X-PACT treatments where the concentrations of drug (psoralen and phosphor) and radiation parameters (energy, dose, and dose rate) were varied. Efficacy was evaluated primarily using flow cell cytometry in combination with complimentary assays, and the in-vivo mouse study. In an in-vitro study, we show that X-PACT induces significant tumor cell apoptosis and cytotoxicity, unlike psoralen or phosphor alone (p<0.0001). We also show that apoptosis increases as doses of phosphor, psoralen, or radiation increase. Finally, in an in-vivo pilot study of BALBc mice with syngeneic 4T1 tumors, we show that the rate of tumor growth is slower with X-PACT than with saline or AMT + X-ray (p<0.0001). Overall these studies demonstrate a potential therapeutic effect for X-PACT, and provide a foundation and rationale for future studies. In summary, X-PACT represents a novel treatment approach in which well-tolerated low doses of x-ray radiation are delivered to a specific tumor site to generate UVA light which in-turn unleashes both short- and potentially long-term antitumor activity of photo-active therapeutics like psoralen. Public Library of Science 2016-09-01 /pmc/articles/PMC5008763/ /pubmed/27583569 http://dx.doi.org/10.1371/journal.pone.0162078 Text en © 2016 Oldham et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Oldham, Mark Yoon, Paul Fathi, Zak Beyer, Wayne F. Adamson, Justus Liu, Leihua Alcorta, David Xia, Wenle Osada, Takuya Liu, Congxiao Yang, Xiao Y. Dodd, Rebecca D. Herndon, James E. Meng, Boyu Kirsch, David G. Lyerly, H. Kim Dewhirst, Mark W. Fecci, Peter Walder, Harold Spector, Neil L. X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title | X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title_full | X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title_fullStr | X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title_full_unstemmed | X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title_short | X-Ray Psoralen Activated Cancer Therapy (X-PACT) |
title_sort | x-ray psoralen activated cancer therapy (x-pact) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008763/ https://www.ncbi.nlm.nih.gov/pubmed/27583569 http://dx.doi.org/10.1371/journal.pone.0162078 |
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