TY - JOUR
T1 - Cold plasma selectivity and the possibility of a paradigm shift in cancer therapy
AU - Keidar, M.
AU - Walk, R.
AU - Shashurin, A.
AU - Srinivasan, P.
AU - Sandler, A.
AU - Dasgupta, S.
AU - Ravi, R.
AU - Guerrero-Preston, R.
AU - Trink, B.
PY - 2011/10/25
Y1 - 2011/10/25
N2 - Background: Plasma is an ionised gas that is typically generated in high-temperature laboratory conditions. However, recent progress in atmospheric plasmas has led to the creation of cold plasmas with ion temperature close to room temperature. Methods: Both in-vitro and in-vivo studies revealed that cold plasmas selectively kill cancer cells. Results: We show that: (a) cold plasma application selectively eradicates cancer cells in vitro without damaging normal cells; and (b) significantly reduces tumour size in vivo. It is shown that reactive oxygen species metabolism and oxidative stress responsive genes are deregulated. Conclusion: The development of cold plasma tumour ablation has the potential of shifting the current paradigm of cancer treatment and enabling the transformation of cancer treatment technologies by utilisation of another state of matter.
AB - Background: Plasma is an ionised gas that is typically generated in high-temperature laboratory conditions. However, recent progress in atmospheric plasmas has led to the creation of cold plasmas with ion temperature close to room temperature. Methods: Both in-vitro and in-vivo studies revealed that cold plasmas selectively kill cancer cells. Results: We show that: (a) cold plasma application selectively eradicates cancer cells in vitro without damaging normal cells; and (b) significantly reduces tumour size in vivo. It is shown that reactive oxygen species metabolism and oxidative stress responsive genes are deregulated. Conclusion: The development of cold plasma tumour ablation has the potential of shifting the current paradigm of cancer treatment and enabling the transformation of cancer treatment technologies by utilisation of another state of matter.
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U2 - 10.1038/bjc.2011.386
DO - 10.1038/bjc.2011.386
M3 - Article
C2 - 21979421
AN - SCOPUS:80054972198
SN - 0007-0920
VL - 105
SP - 1295
EP - 1301
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 9
ER -