Skip to main content
Top
Published in: Tumor Biology 2/2011

01-04-2011 | Research Article

A superficial colon tumor model involving subcutaneous colon translocation and orthotopic transplantation of green fluorescent protein-expressing human colon tumor

Authors: Heiying Jin, Zhijian Yang, Jiangdong Wang, Suying Zhang, Yu Sun, Yijiang Ding

Published in: Tumor Biology | Issue 2/2011

Login to get access

Abstract

The orthotopic transplantation model of human tumor has been demonstrated to be more patient-like animal tumor model. However, observations of tumor progression and metastasis are limited by the deep location of the colon or limited deep penetration ability of fluorescence through tissue. The purpose of this study is to establish a superficial orthotopic model to allow easier real-time visualization and more sensitive monitoring of fluorescent orthotopic colon tumor. Human colon cancer HT-29 cells were transduced with a pLPCX expression retroviral vector containing green fluorescent protein and neomycin resistance genes. For superficial orthotopic transplantation model, the cecum was identified and pulled out of the peritoneal cavity, the space between the cecum and peritoneum was sutured, the cecum was pulled to subcutaneous tissue, and incision was made on the cecal serosa followed by the implantation of a 1-mm tumor tissue to the cecum. For comparison, a conventional orthotopic transplantation model was established in a separate group of mice simultaneously. When tumor sizes reached 5 mm in diameter, half the mice in each model received 5-FU treatment. Primary tumor and metastases were monitored by fluorescent imaging or caliber measurement. Tumor fluorescence was observed as early as 3 days (median time of 4.7 ± 1.3 days) post-transplantation in the superficial orthotopic transplantation model, which was much earlier than 21 days (median time of 26.2 ± 9.9 days) in conventional orthotopic transplantation model. Although tumor growth of 5-FU-treated mice in conventional orthotopic model was lower than those of the untreated mice, the difference was not significant. However, in superficial orthotopic model, tumor growth was significantly inhibited in 5-FU-treated mice relative to the untreated mice. Fluorescence imaging showed similar metastasis incidence between the superficial and conventional orthotopic transplantation models. The fluorescent superficial orthotopic transplantation colon model allows easier real-time visualization and more sensitive monitoring of tumor growth as well as convenient repeated sampling. It is a valuable orthotopic implantation model for study of colon cancer and evaluation of new anti-cancer therapy.
Literature
2.
go back to reference Rho YS, Lee KT, Jung JC, Yoon C, An Z, Hoffman RM, et al. Efficacy of new platinum analog DPPE in an orthotopic nude mouse model of human colon cancer. Anticancer Res. 1999;19:157–62.PubMed Rho YS, Lee KT, Jung JC, Yoon C, An Z, Hoffman RM, et al. Efficacy of new platinum analog DPPE in an orthotopic nude mouse model of human colon cancer. Anticancer Res. 1999;19:157–62.PubMed
3.
go back to reference Ji Y, Hayashi K, Amoh Y, Tsuji K, Yamauchi K, Yamamoto N, et al. The camptothecin derivative CPT-11 inhibits angiogenesis in a dual-color imageable orthotopic metastatic nude mouse model of human colon cancer. Anticancer Res. 2007;27:713–8.PubMed Ji Y, Hayashi K, Amoh Y, Tsuji K, Yamauchi K, Yamamoto N, et al. The camptothecin derivative CPT-11 inhibits angiogenesis in a dual-color imageable orthotopic metastatic nude mouse model of human colon cancer. Anticancer Res. 2007;27:713–8.PubMed
4.
go back to reference Hoffman RM. Orthotopic is orthodox. Why are orthotopic-transplant metastatic models different from all other models? J Cell Biochem. 1994;56:1–3.CrossRefPubMed Hoffman RM. Orthotopic is orthodox. Why are orthotopic-transplant metastatic models different from all other models? J Cell Biochem. 1994;56:1–3.CrossRefPubMed
5.
go back to reference Rashidi B, Sun FX, Jiang P, An Z, Gamagami R, Moossa AR, et al. A nude mouse model of massive liver and lymph node metastasis of human colon cancer. Anticancer Res. 2000;20:715–22.PubMed Rashidi B, Sun FX, Jiang P, An Z, Gamagami R, Moossa AR, et al. A nude mouse model of massive liver and lymph node metastasis of human colon cancer. Anticancer Res. 2000;20:715–22.PubMed
6.
go back to reference Hoffman RM. Orthotopic metastatic (MetaMouse) models for discovery and development of novel chemotherapy. Meth Mol Med. 2005;111:297–322. Hoffman RM. Orthotopic metastatic (MetaMouse) models for discovery and development of novel chemotherapy. Meth Mol Med. 2005;111:297–322.
7.
go back to reference Hoffman RM. Orthotopic transplant mouse models with green fluorescent protein-expressing cancer cells to visualize metastasis and angiogenesis. Cancer Metastasis Rev. 1998–1999;17:271–7.CrossRef Hoffman RM. Orthotopic transplant mouse models with green fluorescent protein-expressing cancer cells to visualize metastasis and angiogenesis. Cancer Metastasis Rev. 1998–1999;17:271–7.CrossRef
8.
go back to reference Marchal F, Tran N, Marchal S, Leroux A, Marchal C, Bolotine L, et al. Development of an HT29 liver metastases model in nude rats. Oncol Rep. 2005;14:1203–7.PubMed Marchal F, Tran N, Marchal S, Leroux A, Marchal C, Bolotine L, et al. Development of an HT29 liver metastases model in nude rats. Oncol Rep. 2005;14:1203–7.PubMed
9.
go back to reference Jin H, Liu X, Li VK, Ding Y, Yun S, Liu F, et al. A simple colostomy implantation model for evaluating colon cancer. Int J Colorectal Dis. 2009;24:41–7.CrossRefPubMed Jin H, Liu X, Li VK, Ding Y, Yun S, Liu F, et al. A simple colostomy implantation model for evaluating colon cancer. Int J Colorectal Dis. 2009;24:41–7.CrossRefPubMed
10.
go back to reference Yamauchi K, Yang M, Jiang P, Xu M, Yamamoto N, Tsuchiya H, et al. Development of real-time subcellular dynamic multicolor imaging of cancer-cell trafficking in live mice with a variable-magnification whole-mouse imaging system. Cancer Res. 2006;66:4208–14.CrossRefPubMed Yamauchi K, Yang M, Jiang P, Xu M, Yamamoto N, Tsuchiya H, et al. Development of real-time subcellular dynamic multicolor imaging of cancer-cell trafficking in live mice with a variable-magnification whole-mouse imaging system. Cancer Res. 2006;66:4208–14.CrossRefPubMed
11.
12.
go back to reference Hoffman RM. The multiple uses of fluorescent proteins to visualize cancer in vivo. Nat Rev Cancer. 2005;5:796–806.CrossRefPubMed Hoffman RM. The multiple uses of fluorescent proteins to visualize cancer in vivo. Nat Rev Cancer. 2005;5:796–806.CrossRefPubMed
Metadata
Title
A superficial colon tumor model involving subcutaneous colon translocation and orthotopic transplantation of green fluorescent protein-expressing human colon tumor
Authors
Heiying Jin
Zhijian Yang
Jiangdong Wang
Suying Zhang
Yu Sun
Yijiang Ding
Publication date
01-04-2011
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 2/2011
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-010-0132-7

Other articles of this Issue 2/2011

Tumor Biology 2/2011 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine