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Preclinical Study of Locoregional Therapy of Hepatocellular Carcinoma by Bioelectric Ablation with Microsecond Pulsed Electric Fields (μsPEFs).

Abstract
Unresectable hepatocellular carcinoma (HCC) needs locoregional ablation as a curative or downstage therapy. Microsecond Pulsed Electric Fields (μsPEFs) is an option. A xenograft tumor model was set up on 48 nude mice by injecting human hepatocellular carcinoma Hep3B cells subcutaneously. The tumor-bearing mice were randomly divided into 3 groups: μsPEFs treated, sham and control group. μsPEFs group was treated by μsPEFs twice in 5 days. Tumor volume, survival, pathology, mitochondria function and cytokines were followed up. μsPEFs was also conducted on 3 swine to determine impact on organ functions. The tumors treated by μsPEFs were completely eradicated while tumors in control and sham groups grew up to 2 cm(3) in 3 weeks. The μsPEFs-treated group indicated mitochondrial damage and tumor necrosis as shown in JC-1 test, flow cytometry, H&E staining and TEM. μsPEFs activates CD56+ and CD68+ cells and inhibits tumor proliferating cell nuclear antigen. μsPEFs inhibits HCC growth in the nude mice by causing mitochondria damage, tumor necrosis and non-specific inflammation. μsPEFs treats porcine livers without damaging vital organs. μsPEFs is a feasible minimally invasive locoregional ablation option.
AuthorsXinhua Chen, Zhigang Ren, Chengxiang Li, Fei Guo, Dianbo Zhou, Jianwen Jiang, Xinmei Chen, Jihong Sun, Chenguo Yao, Shusen Zheng
JournalScientific reports (Sci Rep) Vol. 5 Pg. 9851 (Apr 30 2015) ISSN: 2045-2322 [Electronic] England
PMID25928327 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Proliferating Cell Nuclear Antigen
Topics
  • Animals
  • Apoptosis (physiology)
  • Carcinoma, Hepatocellular (metabolism, therapy)
  • Catheter Ablation (methods)
  • Cell Line, Tumor
  • Humans
  • Liver Neoplasms (metabolism, therapy)
  • Liver Neoplasms, Experimental (metabolism, therapy)
  • Mice
  • Mice, Nude
  • Mitochondria (metabolism)
  • Necrosis (metabolism)
  • Proliferating Cell Nuclear Antigen (metabolism)
  • Tumor Burden (physiology)
  • Xenograft Model Antitumor Assays (methods)

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