Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer
The aim of this study was to monitor changes in the expression of immune-related genes in the bladder after tumor implantation. Mice were orthotopically implanted with MB49-PSA cells (C57BL/6 mice) on day 1 and terminated on days 7, 14, 21, and 28. Another mouse model (MBT-2/C3H mice) was examined...
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2011-01-01
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Series: | Clinical and Developmental Immunology |
Online Access: | http://dx.doi.org/10.1155/2011/865684 |
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doaj-d693edfd0cd644d7b3eb36bdd0a2ad812020-11-24T22:27:51ZengHindawi LimitedClinical and Developmental Immunology1740-25221740-25302011-01-01201110.1155/2011/865684865684Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder CancerSin Mun Tham0Kee Hui Ng1Sim Hwee Pook2Kesavan Esuvaranathan3Ratha Mahendran4Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower Block, Level 8, 119228, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower Block, Level 8, 119228, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower Block, Level 8, 119228, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower Block, Level 8, 119228, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, NUHS Tower Block, Level 8, 119228, SingaporeThe aim of this study was to monitor changes in the expression of immune-related genes in the bladder after tumor implantation. Mice were orthotopically implanted with MB49-PSA cells (C57BL/6 mice) on day 1 and terminated on days 7, 14, 21, and 28. Another mouse model (MBT-2/C3H mice) was examined at day 7. Gene expression analysis was performed using a TaqMan Low Density Mouse Immune Panel (Applied Biosystems, USA) on RNA extracted from the bladders. Selected genes were reconfirmed by real-time PCR analysis and RT-PCR on the mRNA from other animals. Immune suppressive (IL13, IL1β, PTGS2, NOS2, IL10, CTLA4, and CCL22) and immune stimulatory genes (CSF2, GZMB, IFNγ, CXCL10, TNFα, CD80, IL12a, and IL6) and AGTR2 were increased by day 7. By day 28, IL10, CCL2, CCL5, CXCL11, CTLA4, GZMB, IFNγ, CSF2, and IL6 were significantly increased. Therapeutic strategies involving TH1 induction and TH2 dampening may improve responses to immunotherapy.http://dx.doi.org/10.1155/2011/865684 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sin Mun Tham Kee Hui Ng Sim Hwee Pook Kesavan Esuvaranathan Ratha Mahendran |
spellingShingle |
Sin Mun Tham Kee Hui Ng Sim Hwee Pook Kesavan Esuvaranathan Ratha Mahendran Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer Clinical and Developmental Immunology |
author_facet |
Sin Mun Tham Kee Hui Ng Sim Hwee Pook Kesavan Esuvaranathan Ratha Mahendran |
author_sort |
Sin Mun Tham |
title |
Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer |
title_short |
Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer |
title_full |
Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer |
title_fullStr |
Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer |
title_full_unstemmed |
Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer |
title_sort |
tumor and microenvironment modification during progression of murine orthotopic bladder cancer |
publisher |
Hindawi Limited |
series |
Clinical and Developmental Immunology |
issn |
1740-2522 1740-2530 |
publishDate |
2011-01-01 |
description |
The aim of this study was to monitor changes in the expression of immune-related genes in the bladder after tumor implantation. Mice were orthotopically implanted with MB49-PSA cells (C57BL/6 mice) on day 1 and terminated on days 7, 14, 21, and 28. Another mouse model (MBT-2/C3H mice) was examined at day 7. Gene expression analysis was performed using a TaqMan Low Density Mouse Immune Panel (Applied Biosystems, USA) on RNA extracted from the bladders. Selected genes were reconfirmed by real-time PCR analysis and RT-PCR on the mRNA from other animals. Immune suppressive (IL13, IL1β, PTGS2, NOS2, IL10, CTLA4, and CCL22) and immune stimulatory genes (CSF2, GZMB, IFNγ, CXCL10, TNFα, CD80, IL12a, and IL6) and AGTR2 were increased by day 7. By day 28, IL10, CCL2, CCL5, CXCL11, CTLA4, GZMB, IFNγ, CSF2, and IL6 were significantly increased. Therapeutic strategies involving TH1 induction and TH2 dampening may improve responses to immunotherapy. |
url |
http://dx.doi.org/10.1155/2011/865684 |
work_keys_str_mv |
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