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Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities

OBJECTIVES: To evaluate damage effect of High-intensity focused ultrasound on early stage endometrial cancer tissues and their vascularities. MATERIALS AND METHODS: Rabbit endometrial cancer models were established via tumor blocks implantation for a prospective control study. Ultrasonic ablation ef...

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Autores principales: Guan, Liming, Xu, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386707/
https://www.ncbi.nlm.nih.gov/pubmed/28121624
http://dx.doi.org/10.18632/oncotarget.14751
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author Guan, Liming
Xu, Gang
author_facet Guan, Liming
Xu, Gang
author_sort Guan, Liming
collection PubMed
description OBJECTIVES: To evaluate damage effect of High-intensity focused ultrasound on early stage endometrial cancer tissues and their vascularities. MATERIALS AND METHODS: Rabbit endometrial cancer models were established via tumor blocks implantation for a prospective control study. Ultrasonic ablation efficacy was evaluated by pathologic and imaging changes. The target lesions of experimental rabbits before and after ultrasonic ablation were observed after autopsy. The slides were used for hematoxylin-eosin staining, elastic fiber staining and endothelial cell staining; the slides were observed by optical microscopy. One slide was observed by electron microscopy. Then the target lesions of experimental animals with ultrasonic ablation were observed by vascular imaging, one group was visualized by digital subtract angiography, one group was quantified by color Doppler flow imaging, and one group was detected by dye perfusion. SPSS 19.0 software was used for statistical analyses. RESULTS: Histological examination indicated that High-intensity focused ultrasound caused the tumor tissues and their vascularities coagulative necrosis. Tumor vascular structure components including elastic fiber, endothelial cells all were destroyed by ultrasonic ablation. Digital subtract angiography showed tumor vascular shadow were dismissed after ultrasonic ablation. After ultrasonic ablation, gray-scale of tumor nodules enhanced in ultrasonography, tumor peripheral and internal blood flow signals disappeared or significantly reduced in color Doppler flow imaging. Vascular perfusion performed after ultrasonic ablation, tumor vessels could not filled by dye liquid. CONCLUSION: High-intensity focused ultrasound as a noninvasive method can destroy whole endometrial cancer cells and their supplying vascularities, which maybe an alternative approach of targeted therapy and new antiangiogenic strategy for endometrial cancer.
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spelling pubmed-53867072017-04-26 Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities Guan, Liming Xu, Gang Oncotarget Research Paper OBJECTIVES: To evaluate damage effect of High-intensity focused ultrasound on early stage endometrial cancer tissues and their vascularities. MATERIALS AND METHODS: Rabbit endometrial cancer models were established via tumor blocks implantation for a prospective control study. Ultrasonic ablation efficacy was evaluated by pathologic and imaging changes. The target lesions of experimental rabbits before and after ultrasonic ablation were observed after autopsy. The slides were used for hematoxylin-eosin staining, elastic fiber staining and endothelial cell staining; the slides were observed by optical microscopy. One slide was observed by electron microscopy. Then the target lesions of experimental animals with ultrasonic ablation were observed by vascular imaging, one group was visualized by digital subtract angiography, one group was quantified by color Doppler flow imaging, and one group was detected by dye perfusion. SPSS 19.0 software was used for statistical analyses. RESULTS: Histological examination indicated that High-intensity focused ultrasound caused the tumor tissues and their vascularities coagulative necrosis. Tumor vascular structure components including elastic fiber, endothelial cells all were destroyed by ultrasonic ablation. Digital subtract angiography showed tumor vascular shadow were dismissed after ultrasonic ablation. After ultrasonic ablation, gray-scale of tumor nodules enhanced in ultrasonography, tumor peripheral and internal blood flow signals disappeared or significantly reduced in color Doppler flow imaging. Vascular perfusion performed after ultrasonic ablation, tumor vessels could not filled by dye liquid. CONCLUSION: High-intensity focused ultrasound as a noninvasive method can destroy whole endometrial cancer cells and their supplying vascularities, which maybe an alternative approach of targeted therapy and new antiangiogenic strategy for endometrial cancer. Impact Journals LLC 2017-01-19 /pmc/articles/PMC5386707/ /pubmed/28121624 http://dx.doi.org/10.18632/oncotarget.14751 Text en Copyright: © 2017 Guan and Xu http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Guan, Liming
Xu, Gang
Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title_full Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title_fullStr Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title_full_unstemmed Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title_short Destructive effect of HIFU on rabbit embedded endometrial carcinoma tissues and their vascularities
title_sort destructive effect of hifu on rabbit embedded endometrial carcinoma tissues and their vascularities
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386707/
https://www.ncbi.nlm.nih.gov/pubmed/28121624
http://dx.doi.org/10.18632/oncotarget.14751
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