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Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma

BACKGROUND: We tested the hypothesis that radiofrequency ablation (RFA) for hepatocellular carcinoma (HCC) promotes tumor cell release and explored a method for reducing these effects. METHODS: A green fluorescent protein-transfected orthotopic HCC model was established in 99 nude mice. In vivo flow...

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Autores principales: Zhuang, Bowen, Zhu, Xi, Lin, Jinhua, Zhang, Fuli, Qiao, Bin, Kang, Jihui, Xie, Xiaohua, Wei, Xunbin, Xie, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686970/
https://www.ncbi.nlm.nih.gov/pubmed/38019353
http://dx.doi.org/10.1186/s41747-023-00382-5
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author Zhuang, Bowen
Zhu, Xi
Lin, Jinhua
Zhang, Fuli
Qiao, Bin
Kang, Jihui
Xie, Xiaohua
Wei, Xunbin
Xie, Xiaoyan
author_facet Zhuang, Bowen
Zhu, Xi
Lin, Jinhua
Zhang, Fuli
Qiao, Bin
Kang, Jihui
Xie, Xiaohua
Wei, Xunbin
Xie, Xiaoyan
author_sort Zhuang, Bowen
collection PubMed
description BACKGROUND: We tested the hypothesis that radiofrequency ablation (RFA) for hepatocellular carcinoma (HCC) promotes tumor cell release and explored a method for reducing these effects. METHODS: A green fluorescent protein-transfected orthotopic HCC model was established in 99 nude mice. In vivo flow cytometry was used to monitor circulating tumor cell (CTC) dynamics. Pulmonary fluorescence imaging and pathology were performed to investigate lung metastases. First, the kinetics of CTCs during the periablation period and the survival rate of CTCs released during RFA were investigated. Next, mice were allocated to controls, sham ablation, or RFA with/without hepatic vessel blocking (ligation of the portal triads) for evaluating the postablation CTC level, lung metastases, and survival over time. Moreover, the kinetics of CTCs, lung metastases, and mice survival were evaluated for RFA with/without ethanol injection. Pathological changes in tumors and surrounding parenchyma after ethanol injection were noted. Statistical analysis included t-test, ANOVA, and Kaplan-Meier survival curves. RESULTS: CTC counts were 12.3-fold increased during RFA, and 73.7% of RFA-induced CTCs were viable. Pre-RFA hepatic vessel blocking prevented the increase of peripheral CTCs, reduced the number of lung metastases, and prolonged survival (all p ≤ 0.05). Similarly, pre-RFA ethanol injection remarkably decreased CTC release during RFA and further decreased lung metastases with extended survival (all p ≤ 0.05). Histopathology revealed thrombus formation in blood vessels after ethanol injection, which may clog tumor cell dissemination during RFA. CONCLUSION: RFA induces viable tumor cell dissemination, and pre-RFA ethanol injection may provide a prophylactic strategy to reduce this underestimated effect. RELEVANCE STATEMENT: RFA for HCC promotes viable tumor cell release during ablation, while ethanol injection can prevent RFA induced tumor cell release. KEY POINTS: • RFA induced the release of viable tumor cells during the ablation procedure in an animal model. • Hepatic vessel blocking can suppress tumor cells dissemination during RFA. • Ethanol injection can prevent RFA-induced tumor cell release, presumably because of the formation of thrombosis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41747-023-00382-5.
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spelling pubmed-106869702023-11-30 Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma Zhuang, Bowen Zhu, Xi Lin, Jinhua Zhang, Fuli Qiao, Bin Kang, Jihui Xie, Xiaohua Wei, Xunbin Xie, Xiaoyan Eur Radiol Exp Original Article BACKGROUND: We tested the hypothesis that radiofrequency ablation (RFA) for hepatocellular carcinoma (HCC) promotes tumor cell release and explored a method for reducing these effects. METHODS: A green fluorescent protein-transfected orthotopic HCC model was established in 99 nude mice. In vivo flow cytometry was used to monitor circulating tumor cell (CTC) dynamics. Pulmonary fluorescence imaging and pathology were performed to investigate lung metastases. First, the kinetics of CTCs during the periablation period and the survival rate of CTCs released during RFA were investigated. Next, mice were allocated to controls, sham ablation, or RFA with/without hepatic vessel blocking (ligation of the portal triads) for evaluating the postablation CTC level, lung metastases, and survival over time. Moreover, the kinetics of CTCs, lung metastases, and mice survival were evaluated for RFA with/without ethanol injection. Pathological changes in tumors and surrounding parenchyma after ethanol injection were noted. Statistical analysis included t-test, ANOVA, and Kaplan-Meier survival curves. RESULTS: CTC counts were 12.3-fold increased during RFA, and 73.7% of RFA-induced CTCs were viable. Pre-RFA hepatic vessel blocking prevented the increase of peripheral CTCs, reduced the number of lung metastases, and prolonged survival (all p ≤ 0.05). Similarly, pre-RFA ethanol injection remarkably decreased CTC release during RFA and further decreased lung metastases with extended survival (all p ≤ 0.05). Histopathology revealed thrombus formation in blood vessels after ethanol injection, which may clog tumor cell dissemination during RFA. CONCLUSION: RFA induces viable tumor cell dissemination, and pre-RFA ethanol injection may provide a prophylactic strategy to reduce this underestimated effect. RELEVANCE STATEMENT: RFA for HCC promotes viable tumor cell release during ablation, while ethanol injection can prevent RFA induced tumor cell release. KEY POINTS: • RFA induced the release of viable tumor cells during the ablation procedure in an animal model. • Hepatic vessel blocking can suppress tumor cells dissemination during RFA. • Ethanol injection can prevent RFA-induced tumor cell release, presumably because of the formation of thrombosis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41747-023-00382-5. Springer Vienna 2023-11-29 /pmc/articles/PMC10686970/ /pubmed/38019353 http://dx.doi.org/10.1186/s41747-023-00382-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Zhuang, Bowen
Zhu, Xi
Lin, Jinhua
Zhang, Fuli
Qiao, Bin
Kang, Jihui
Xie, Xiaohua
Wei, Xunbin
Xie, Xiaoyan
Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title_full Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title_fullStr Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title_full_unstemmed Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title_short Radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
title_sort radiofrequency ablation induces tumor cell dissemination in a mouse model of hepatocellular carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686970/
https://www.ncbi.nlm.nih.gov/pubmed/38019353
http://dx.doi.org/10.1186/s41747-023-00382-5
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