TY - JOUR
T1 - Cold atmospheric plasma for the ablative treatment of neuroblastoma
AU - Walk, Ryan M.
AU - Snyder, Jason A.
AU - Srinivasan, Priya
AU - Kirsch, Jacob
AU - Diaz, Stephanie O.
AU - Blanco, Felix C.
AU - Shashurin, Alexey
AU - Keidar, Michael
AU - Sandler, Anthony D.
PY - 2013/1
Y1 - 2013/1
N2 - Background: Recent breakthroughs have allowed for production of plasma at room temperature. Cold atmospheric plasma (CAP) may offer the capability of delivering reactive oxygen species directly into tissues, representing a novel modality for targeted cancer therapy. We studied helium-based CAP's effect on neuroblastoma, both in-vitro and in an in-vivo murine model. Methods: Mouse neuroblastoma cultures were treated with CAP for 0, 30, 60, and 120 s and assayed for apoptotic and metabolic activity immediately and at 24 and 48 h post-treatment. Five-millimeter tumors were ablated with a single transdermal CAP treatment, and tumor volume and mouse survival were measured. Results: CAP decreased metabolic activity, induced apoptosis, and reduced viability of cancer cells in proportion to both duration of exposure and time post-treatment. In-vivo, a single treatment ablated tumors and eventual tumor growth was decelerated. Furthermore, survival nearly doubled, with median survival of 15 vs. 28 days (p < 0.001). Conclusions: Our findings demonstrate the sensitivity of neuroblastoma to CAP treatment, both in-vitro and in an in-vivo mouse model of established tumor. While further investigation is necessary to establish the mechanism and optimize the treatment protocol, these initial observations establish cold atmospheric plasma as a potentially useful ablative therapy in neuroblastoma.
AB - Background: Recent breakthroughs have allowed for production of plasma at room temperature. Cold atmospheric plasma (CAP) may offer the capability of delivering reactive oxygen species directly into tissues, representing a novel modality for targeted cancer therapy. We studied helium-based CAP's effect on neuroblastoma, both in-vitro and in an in-vivo murine model. Methods: Mouse neuroblastoma cultures were treated with CAP for 0, 30, 60, and 120 s and assayed for apoptotic and metabolic activity immediately and at 24 and 48 h post-treatment. Five-millimeter tumors were ablated with a single transdermal CAP treatment, and tumor volume and mouse survival were measured. Results: CAP decreased metabolic activity, induced apoptosis, and reduced viability of cancer cells in proportion to both duration of exposure and time post-treatment. In-vivo, a single treatment ablated tumors and eventual tumor growth was decelerated. Furthermore, survival nearly doubled, with median survival of 15 vs. 28 days (p < 0.001). Conclusions: Our findings demonstrate the sensitivity of neuroblastoma to CAP treatment, both in-vitro and in an in-vivo mouse model of established tumor. While further investigation is necessary to establish the mechanism and optimize the treatment protocol, these initial observations establish cold atmospheric plasma as a potentially useful ablative therapy in neuroblastoma.
KW - CAP
KW - Cold Atmospheric Plasma
KW - ROS
KW - Reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=84872378171&partnerID=8YFLogxK
U2 - 10.1016/j.jpedsurg.2012.10.020
DO - 10.1016/j.jpedsurg.2012.10.020
M3 - Article
C2 - 23331795
AN - SCOPUS:84872378171
SN - 0022-3468
VL - 48
SP - 67
EP - 73
JO - Journal of Pediatric Surgery
JF - Journal of Pediatric Surgery
IS - 1
ER -