Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.

<h4>Background</h4>Liver tumor remains an important cause of cancer-related death. Nanosecond pulsed electric fields (nsPEFs) are advantageous in the treatment of melanoma and pancreatic cancer, but their therapeutic application on liver tumors need to be further studied.<h4>Method...

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Main Authors: Qing-Gang Li, Zhen-Guo Liu, Gang Dong, Ying Sun, Ya-Wen Zou, Xiao-Long Chen, Bin Wu, Xin-Hua Chen, Zhi-Gang Ren
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0273754
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author Qing-Gang Li
Zhen-Guo Liu
Gang Dong
Ying Sun
Ya-Wen Zou
Xiao-Long Chen
Bin Wu
Xin-Hua Chen
Zhi-Gang Ren
author_facet Qing-Gang Li
Zhen-Guo Liu
Gang Dong
Ying Sun
Ya-Wen Zou
Xiao-Long Chen
Bin Wu
Xin-Hua Chen
Zhi-Gang Ren
author_sort Qing-Gang Li
collection DOAJ
description <h4>Background</h4>Liver tumor remains an important cause of cancer-related death. Nanosecond pulsed electric fields (nsPEFs) are advantageous in the treatment of melanoma and pancreatic cancer, but their therapeutic application on liver tumors need to be further studied.<h4>Methods</h4>Hep3B cells were treated with nsPEFs. The biological behaviors of cells were detected by Cell Counting Kit-8, 5-ethynyl-20-deoxyuridine, and transmission electron microscopy (TEM) assays. In vivo, rabbit VX2 liver tumor models were ablated by ultrasound-guided nsPEFs and radiofrequency ablation (RFA). Contrast-enhanced ultrasound (CEUS) was used to evaluate the ablation effect. HE staining and Masson staining were used to evaluate the tissue morphology after ablation. Immunohistochemistry was performed to determine the expression of Ki67, proliferating cell nuclear antigen, and α-smooth muscle actin at different time points after ablation.<h4>Results</h4>The cell viability of Hep3B cells was continuously lower than that of the control group within 3 days after pulse treatment. The proliferation of Hep3B cells was significantly affected by nsPEFs. TEM showed that Hep3B cells underwent significant morphological changes after pulse treatment. In vivo, CEUS imaging showed that nsPEFs could completely ablate model rabbit VX2 liver tumors. After nsPEFs ablation, the area of tumor fibrosis and the expression of Ki67, proliferating cell nuclear antigen, and α-smooth muscle actin were decreased. However, after RFA, rabbit VX2 liver tumor tissue showed complete necrosis, but the expression of PCNA and α-smooth muscle actin did not decrease compared to the tumor group.<h4>Conclusions</h4>nsPEFs can induce Hep3B cells apoptosis and ablate rabbit VX2 liver tumors in a non-thermal manner versus RFA. The ultrasound contrast agent can monitor immediate effect of nsPEF ablation. This study provides a basis for the clinical study of nsPEFs ablation of liver cancer.
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spelling doaj.art-461a39d4e1b94946b7b7aa6db4d301562023-04-12T05:32:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01183e027375410.1371/journal.pone.0273754Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.Qing-Gang LiZhen-Guo LiuGang DongYing SunYa-Wen ZouXiao-Long ChenBin WuXin-Hua ChenZhi-Gang Ren<h4>Background</h4>Liver tumor remains an important cause of cancer-related death. Nanosecond pulsed electric fields (nsPEFs) are advantageous in the treatment of melanoma and pancreatic cancer, but their therapeutic application on liver tumors need to be further studied.<h4>Methods</h4>Hep3B cells were treated with nsPEFs. The biological behaviors of cells were detected by Cell Counting Kit-8, 5-ethynyl-20-deoxyuridine, and transmission electron microscopy (TEM) assays. In vivo, rabbit VX2 liver tumor models were ablated by ultrasound-guided nsPEFs and radiofrequency ablation (RFA). Contrast-enhanced ultrasound (CEUS) was used to evaluate the ablation effect. HE staining and Masson staining were used to evaluate the tissue morphology after ablation. Immunohistochemistry was performed to determine the expression of Ki67, proliferating cell nuclear antigen, and α-smooth muscle actin at different time points after ablation.<h4>Results</h4>The cell viability of Hep3B cells was continuously lower than that of the control group within 3 days after pulse treatment. The proliferation of Hep3B cells was significantly affected by nsPEFs. TEM showed that Hep3B cells underwent significant morphological changes after pulse treatment. In vivo, CEUS imaging showed that nsPEFs could completely ablate model rabbit VX2 liver tumors. After nsPEFs ablation, the area of tumor fibrosis and the expression of Ki67, proliferating cell nuclear antigen, and α-smooth muscle actin were decreased. However, after RFA, rabbit VX2 liver tumor tissue showed complete necrosis, but the expression of PCNA and α-smooth muscle actin did not decrease compared to the tumor group.<h4>Conclusions</h4>nsPEFs can induce Hep3B cells apoptosis and ablate rabbit VX2 liver tumors in a non-thermal manner versus RFA. The ultrasound contrast agent can monitor immediate effect of nsPEF ablation. This study provides a basis for the clinical study of nsPEFs ablation of liver cancer.https://doi.org/10.1371/journal.pone.0273754
spellingShingle Qing-Gang Li
Zhen-Guo Liu
Gang Dong
Ying Sun
Ya-Wen Zou
Xiao-Long Chen
Bin Wu
Xin-Hua Chen
Zhi-Gang Ren
Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
PLoS ONE
title Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
title_full Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
title_fullStr Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
title_full_unstemmed Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
title_short Nanosecond pulsed electric field ablates rabbit VX2 liver tumors in a non-thermal manner.
title_sort nanosecond pulsed electric field ablates rabbit vx2 liver tumors in a non thermal manner
url https://doi.org/10.1371/journal.pone.0273754
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