Cargando…

A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema

Head and neck lymphedema (HNL) is a disfiguring disease affecting over 90% of patients treated for head and neck cancer. Animal models of lymphedema are used to test pharmacologic and microsurgical therapies; however, no animal model for HNL is described in the literature to date. In this study we d...

Descripción completa

Detalles Bibliográficos
Autores principales: Daneshgaran, Giulia, Lo, Andrea Y., Paik, Connie B., Cooper, Michael N., Sung, Cynthia, Jiao, Wan, Park, Sun Y., Ni, Pauline, Yu, Roy P., Vorobyova, Ivetta, Jashashvili, Tea, Hong, Young-Kwon, Kim, Gene H., Conti, Peter S., Chai, Yang, Wong, Alex K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892928/
https://www.ncbi.nlm.nih.gov/pubmed/31797883
http://dx.doi.org/10.1038/s41598-019-54201-2
_version_ 1783476113865965568
author Daneshgaran, Giulia
Lo, Andrea Y.
Paik, Connie B.
Cooper, Michael N.
Sung, Cynthia
Jiao, Wan
Park, Sun Y.
Ni, Pauline
Yu, Roy P.
Vorobyova, Ivetta
Jashashvili, Tea
Hong, Young-Kwon
Kim, Gene H.
Conti, Peter S.
Chai, Yang
Wong, Alex K.
author_facet Daneshgaran, Giulia
Lo, Andrea Y.
Paik, Connie B.
Cooper, Michael N.
Sung, Cynthia
Jiao, Wan
Park, Sun Y.
Ni, Pauline
Yu, Roy P.
Vorobyova, Ivetta
Jashashvili, Tea
Hong, Young-Kwon
Kim, Gene H.
Conti, Peter S.
Chai, Yang
Wong, Alex K.
author_sort Daneshgaran, Giulia
collection PubMed
description Head and neck lymphedema (HNL) is a disfiguring disease affecting over 90% of patients treated for head and neck cancer. Animal models of lymphedema are used to test pharmacologic and microsurgical therapies; however, no animal model for HNL is described in the literature to date. In this study we describe the first reproducible rat model for HNL. Animals were subjected to two surgical protocols: (1) lymphadenectomy plus irradiation; and (2) sham surgery and no irradiation. Head and neck expansion was measured on post-operative days 15, 30 and 60. Magnetic resonance imaging (MRI) was acquired at the same time points. Lymphatic drainage was measured at day 60 via indocyanine green (ICG) lymphography, after which animals were sacrificed for histological analysis. Postsurgical lymphedema was observed 100% of the time. Compared to sham-operated animals, lymphadenectomy animals experienced significantly more head and neck swelling at all timepoints (P < 0.01). Lymphadenectomy animals had significantly slower lymphatic drainage for 6 days post-ICG injection (P < 0.05). Histological analysis of lymphadenectomy animals revealed 83% greater subcutis thickness (P = 0.008), 22% greater collagen deposition (P = 0.001), 110% greater TGFβ1(+) cell density (P = 0(.)04), 1.7-fold increase in TGFβ1 mRNA expression (P = 0.03), and 114% greater T-cell infiltration (P = 0.005) compared to sham-operated animals. In conclusion, animals subjected to complete lymph node dissection and irradiation developed changes consistent with human clinical postsurgical HNL. This was evidenced by significant increase in all head and neck measurements, slower lymphatic drainage, subcutaneous tissue expansion, increased fibrosis, and increased inflammation compared to sham-operated animals.
format Online
Article
Text
id pubmed-6892928
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-68929282019-12-11 A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema Daneshgaran, Giulia Lo, Andrea Y. Paik, Connie B. Cooper, Michael N. Sung, Cynthia Jiao, Wan Park, Sun Y. Ni, Pauline Yu, Roy P. Vorobyova, Ivetta Jashashvili, Tea Hong, Young-Kwon Kim, Gene H. Conti, Peter S. Chai, Yang Wong, Alex K. Sci Rep Article Head and neck lymphedema (HNL) is a disfiguring disease affecting over 90% of patients treated for head and neck cancer. Animal models of lymphedema are used to test pharmacologic and microsurgical therapies; however, no animal model for HNL is described in the literature to date. In this study we describe the first reproducible rat model for HNL. Animals were subjected to two surgical protocols: (1) lymphadenectomy plus irradiation; and (2) sham surgery and no irradiation. Head and neck expansion was measured on post-operative days 15, 30 and 60. Magnetic resonance imaging (MRI) was acquired at the same time points. Lymphatic drainage was measured at day 60 via indocyanine green (ICG) lymphography, after which animals were sacrificed for histological analysis. Postsurgical lymphedema was observed 100% of the time. Compared to sham-operated animals, lymphadenectomy animals experienced significantly more head and neck swelling at all timepoints (P < 0.01). Lymphadenectomy animals had significantly slower lymphatic drainage for 6 days post-ICG injection (P < 0.05). Histological analysis of lymphadenectomy animals revealed 83% greater subcutis thickness (P = 0.008), 22% greater collagen deposition (P = 0.001), 110% greater TGFβ1(+) cell density (P = 0(.)04), 1.7-fold increase in TGFβ1 mRNA expression (P = 0.03), and 114% greater T-cell infiltration (P = 0.005) compared to sham-operated animals. In conclusion, animals subjected to complete lymph node dissection and irradiation developed changes consistent with human clinical postsurgical HNL. This was evidenced by significant increase in all head and neck measurements, slower lymphatic drainage, subcutaneous tissue expansion, increased fibrosis, and increased inflammation compared to sham-operated animals. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892928/ /pubmed/31797883 http://dx.doi.org/10.1038/s41598-019-54201-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Daneshgaran, Giulia
Lo, Andrea Y.
Paik, Connie B.
Cooper, Michael N.
Sung, Cynthia
Jiao, Wan
Park, Sun Y.
Ni, Pauline
Yu, Roy P.
Vorobyova, Ivetta
Jashashvili, Tea
Hong, Young-Kwon
Kim, Gene H.
Conti, Peter S.
Chai, Yang
Wong, Alex K.
A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title_full A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title_fullStr A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title_full_unstemmed A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title_short A Pre-clinical Animal Model of Secondary Head and Neck Lymphedema
title_sort pre-clinical animal model of secondary head and neck lymphedema
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892928/
https://www.ncbi.nlm.nih.gov/pubmed/31797883
http://dx.doi.org/10.1038/s41598-019-54201-2
work_keys_str_mv AT daneshgarangiulia apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT loandreay apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT paikconnieb apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT coopermichaeln apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT sungcynthia apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT jiaowan apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT parksuny apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT nipauline apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT yuroyp apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT vorobyovaivetta apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT jashashvilitea apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT hongyoungkwon apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT kimgeneh apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT contipeters apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT chaiyang apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT wongalexk apreclinicalanimalmodelofsecondaryheadandnecklymphedema
AT daneshgarangiulia preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT loandreay preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT paikconnieb preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT coopermichaeln preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT sungcynthia preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT jiaowan preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT parksuny preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT nipauline preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT yuroyp preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT vorobyovaivetta preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT jashashvilitea preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT hongyoungkwon preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT kimgeneh preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT contipeters preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT chaiyang preclinicalanimalmodelofsecondaryheadandnecklymphedema
AT wongalexk preclinicalanimalmodelofsecondaryheadandnecklymphedema