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An orthotopic mouse model of gastric cancer invasion and metastasis

Gastric cancer is a leading cause of cancer death worldwide, with advanced stage being correlated to the level of tumour invasion and metastasis. Current research is heavily focused on the identification and development of efficacious therapeutics targeting these fundamental hallmarks of cancer, how...

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Autores principales: Busuttil, Rita A., Liu, David S., Di Costanzo, Natasha, Schröder, Jan, Mitchell, Catherine, Boussioutas, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770387/
https://www.ncbi.nlm.nih.gov/pubmed/29339747
http://dx.doi.org/10.1038/s41598-017-19025-y
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author Busuttil, Rita A.
Liu, David S.
Di Costanzo, Natasha
Schröder, Jan
Mitchell, Catherine
Boussioutas, Alex
author_facet Busuttil, Rita A.
Liu, David S.
Di Costanzo, Natasha
Schröder, Jan
Mitchell, Catherine
Boussioutas, Alex
author_sort Busuttil, Rita A.
collection PubMed
description Gastric cancer is a leading cause of cancer death worldwide, with advanced stage being correlated to the level of tumour invasion and metastasis. Current research is heavily focused on the identification and development of efficacious therapeutics targeting these fundamental hallmarks of cancer, however there are currently no animal models that mimic the invasive phenotypes observed in humans. To address this we have developed an orthotopic mouse model whereby gastric cancer cell lines are tagged with luciferase and injected into the subserosal layer of the stomach. This allows for the monitoring of primary tumour growth and metastasis in real-time as well as quantitation of the degree of tumour invasion through the stomach wall by immunohistochemistry. We have three models based on the degree of invasion and metastasis that are cell line specific: The AGS cells develop into invasive tumours by 4-weeks with no evidence of metastases, MKN45 cells are moderately metastatic with minimal invasion till week 2 and MKN28 cells are highly metastatic and fully invasive by week 1. These models have utility as a tool for testing the efficacy of anti-tumour, anti-invasive and anti-metastatic therapies in the setting of gastric cancer, which currently has poor treatment options.
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spelling pubmed-57703872018-01-25 An orthotopic mouse model of gastric cancer invasion and metastasis Busuttil, Rita A. Liu, David S. Di Costanzo, Natasha Schröder, Jan Mitchell, Catherine Boussioutas, Alex Sci Rep Article Gastric cancer is a leading cause of cancer death worldwide, with advanced stage being correlated to the level of tumour invasion and metastasis. Current research is heavily focused on the identification and development of efficacious therapeutics targeting these fundamental hallmarks of cancer, however there are currently no animal models that mimic the invasive phenotypes observed in humans. To address this we have developed an orthotopic mouse model whereby gastric cancer cell lines are tagged with luciferase and injected into the subserosal layer of the stomach. This allows for the monitoring of primary tumour growth and metastasis in real-time as well as quantitation of the degree of tumour invasion through the stomach wall by immunohistochemistry. We have three models based on the degree of invasion and metastasis that are cell line specific: The AGS cells develop into invasive tumours by 4-weeks with no evidence of metastases, MKN45 cells are moderately metastatic with minimal invasion till week 2 and MKN28 cells are highly metastatic and fully invasive by week 1. These models have utility as a tool for testing the efficacy of anti-tumour, anti-invasive and anti-metastatic therapies in the setting of gastric cancer, which currently has poor treatment options. Nature Publishing Group UK 2018-01-16 /pmc/articles/PMC5770387/ /pubmed/29339747 http://dx.doi.org/10.1038/s41598-017-19025-y Text en © The Author(s) 2018 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
Busuttil, Rita A.
Liu, David S.
Di Costanzo, Natasha
Schröder, Jan
Mitchell, Catherine
Boussioutas, Alex
An orthotopic mouse model of gastric cancer invasion and metastasis
title An orthotopic mouse model of gastric cancer invasion and metastasis
title_full An orthotopic mouse model of gastric cancer invasion and metastasis
title_fullStr An orthotopic mouse model of gastric cancer invasion and metastasis
title_full_unstemmed An orthotopic mouse model of gastric cancer invasion and metastasis
title_short An orthotopic mouse model of gastric cancer invasion and metastasis
title_sort orthotopic mouse model of gastric cancer invasion and metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770387/
https://www.ncbi.nlm.nih.gov/pubmed/29339747
http://dx.doi.org/10.1038/s41598-017-19025-y
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