Title
Sensitization Of Pancreatic Cancer Cells To Radiation By Cerium Oxide Nanoparticle-Induced Ros Production
Keywords
Cerium oxide nanoparticles; Pancreatic cancer; Radiation; ROS; Sensitizer
Abstract
Side effect of radiation therapy (RT) remains the most challenging issue for pancreatic cancer treatment. In this report we determined whether and how cerium oxide nanoparticles (CONPs) sensitize pancreatic cancer cells to RT. CONP pretreatment enhanced radiation-induced reactive oxygen species (ROS) production preferentially in acidic cell-free solutions as well as acidic human pancreatic cancer cells. In acidic environments, CONPs favor the scavenging of superoxide radical over the hydroxyl peroxide resulting in accumulation of the latter whereas in neutral pH CONPs scavenge both. CONP treatment prior to RT markedly potentiated the cancer cell apoptosis both in culture and in tumors and the inhibition of the pancreatic tumor growth without harming the normal tissues or host mice. Taken together, these results identify CONPs as a potentially novel RT-sensitizer as well as protectant for improving pancreatic cancer treatment. From the Clinical Editor: Pancreatic tumors remain some of the most notoriously treatment-unresponsive malignancies. Cerium oxide nanoparticles may be capable of sensitizing such cells to radiotherapy, as demonstrated in this study. © 2013 Elsevier Inc.
Publication Date
5-1-2013
Publication Title
Nanomedicine: Nanotechnology, Biology, and Medicine
Volume
9
Issue
4
Number of Pages
558-569
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1016/j.nano.2012.10.010
Copyright Status
Unknown
Socpus ID
84876707046 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84876707046
STARS Citation
Wason, Melissa S.; Colon, Jimmie; Das, Soumen; Seal, Sudipta; and Turkson, James, "Sensitization Of Pancreatic Cancer Cells To Radiation By Cerium Oxide Nanoparticle-Induced Ros Production" (2013). Scopus Export 2010-2014. 6896.
https://stars.library.ucf.edu/scopus2010/6896