X-Ray Psoralen Activated Cancer Therapy (X-PACT).

dc.contributor.author

Oldham, Mark

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Yoon, Paul

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Fathi, Zak

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Beyer, Wayne F

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Adamson, Justus

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Liu, Leihua

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Alcorta, David

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Xia, Wenle

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Osada, Takuya

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Liu, Congxiao

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Yang, Xiao Y

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Dodd, Rebecca D

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Herndon, James E

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Meng, Boyu

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Kirsch, David G

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Lyerly, H Kim

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Dewhirst, Mark W

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Fecci, Peter

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Walder, Harold

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Spector, Neil L

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Lebedeva, Irina V

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United States

dc.date.accessioned

2016-12-01T14:18:39Z

dc.date.issued

2016

dc.description.abstract

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.

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/27583569

dc.identifier

PONE-D-15-48311

dc.identifier.eissn

1932-6203

dc.identifier.uri

https://hdl.handle.net/10161/13034

dc.language

eng

dc.publisher

Public Library of Science (PLoS)

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PLoS One

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10.1371/journal.pone.0162078

dc.title

X-Ray Psoralen Activated Cancer Therapy (X-PACT).

dc.type

Journal article

duke.contributor.orcid

Adamson, Justus|0000-0002-7868-5631

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Lyerly, H Kim|0000-0002-0063-4770

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Dewhirst, Mark W|0000-0003-3459-6546

duke.contributor.orcid

Fecci, Peter|0000-0002-2912-8695

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/27583569

pubs.begin-page

e0162078

pubs.issue

9

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Basic Science Departments

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Biostatistics & Bioinformatics

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Clinical Science Departments

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Duke

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Duke Cancer Institute

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Global Health Institute

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Immunology

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Institutes and Centers

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Institutes and Provost's Academic Units

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Medicine

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Medicine, Medical Oncology

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Pathology

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Pharmacology & Cancer Biology

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Radiation Oncology

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School of Medicine

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Surgery

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Surgery, Surgical Oncology Molecular Theraputics

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University Institutes and Centers

pubs.publication-status

Published online

pubs.volume

11

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