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Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer

Metastases are largely responsible for cancer deaths in solid tumors due to the lack of effective therapies against disseminated disease, and there is an urgent need to fill this gap. This study demonstrates an orthotopic colorectal cancer (CRC) mouse model system to develop spontaneous metastasis i...

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Autores principales: Rajput, Ashwani, Agarwal, Ekta, Leiphrakpam, Premila, Brattain, Michael G., Chowdhury, Sanjib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907346/
https://www.ncbi.nlm.nih.gov/pubmed/27340651
http://dx.doi.org/10.1155/2013/206875
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author Rajput, Ashwani
Agarwal, Ekta
Leiphrakpam, Premila
Brattain, Michael G.
Chowdhury, Sanjib
author_facet Rajput, Ashwani
Agarwal, Ekta
Leiphrakpam, Premila
Brattain, Michael G.
Chowdhury, Sanjib
author_sort Rajput, Ashwani
collection PubMed
description Metastases are largely responsible for cancer deaths in solid tumors due to the lack of effective therapies against disseminated disease, and there is an urgent need to fill this gap. This study demonstrates an orthotopic colorectal cancer (CRC) mouse model system to develop spontaneous metastasis in vivo and compare its reproducibility against human CRC. IGF1R-dependent GEO human CRC cells were used to study metastatic colonization using orthotopic transplantation procedures and demonstrated robust liver metastasis. Cell proliferation assays were performed both in the orthotopic primary colon and liver metastatic tumors, and human CRC patient's specimen and similar patterns in H&E and Ki67 staining were observed between the orthotopically generated primary and liver metastatic tumors and human CRC specimens. Microarray analysis was performed to generate gene signatures, compared with deposited human CRC gene expression data sets, analyzed by Oncomine, and revealed similarity in gene signatures with increased aggressive markers expression associated with CRC in orthotopically generated liver metastasis. Thus, we have developed an orthotopic mouse model that reproduces human CRC metastasis. This model system can be effective in developing new therapeutic strategies against disseminated disease and could be implemented for identifying genes that regulate the development and/or maintenance of established metastasis.
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spelling pubmed-49073462016-06-23 Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer Rajput, Ashwani Agarwal, Ekta Leiphrakpam, Premila Brattain, Michael G. Chowdhury, Sanjib ISRN Hepatol Research Article Metastases are largely responsible for cancer deaths in solid tumors due to the lack of effective therapies against disseminated disease, and there is an urgent need to fill this gap. This study demonstrates an orthotopic colorectal cancer (CRC) mouse model system to develop spontaneous metastasis in vivo and compare its reproducibility against human CRC. IGF1R-dependent GEO human CRC cells were used to study metastatic colonization using orthotopic transplantation procedures and demonstrated robust liver metastasis. Cell proliferation assays were performed both in the orthotopic primary colon and liver metastatic tumors, and human CRC patient's specimen and similar patterns in H&E and Ki67 staining were observed between the orthotopically generated primary and liver metastatic tumors and human CRC specimens. Microarray analysis was performed to generate gene signatures, compared with deposited human CRC gene expression data sets, analyzed by Oncomine, and revealed similarity in gene signatures with increased aggressive markers expression associated with CRC in orthotopically generated liver metastasis. Thus, we have developed an orthotopic mouse model that reproduces human CRC metastasis. This model system can be effective in developing new therapeutic strategies against disseminated disease and could be implemented for identifying genes that regulate the development and/or maintenance of established metastasis. Hindawi Publishing Corporation 2013-04-21 /pmc/articles/PMC4907346/ /pubmed/27340651 http://dx.doi.org/10.1155/2013/206875 Text en Copyright © 2013 Ashwani Rajput et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rajput, Ashwani
Agarwal, Ekta
Leiphrakpam, Premila
Brattain, Michael G.
Chowdhury, Sanjib
Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title_full Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title_fullStr Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title_full_unstemmed Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title_short Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer
title_sort establishment and validation of an orthotopic metastatic mouse model of colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907346/
https://www.ncbi.nlm.nih.gov/pubmed/27340651
http://dx.doi.org/10.1155/2013/206875
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