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Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model
The aim of this study was to establish a tumor model in mice with the expression of luciferase (Luc) and human prostate stem cell antigen (PSCA), in order to evaluate the activities of anticancer drugs or vaccines for prostate cancer. RM-1 cells were stably transfected with pcDNA-Luc and pcDNA-PSCA...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820663/ https://www.ncbi.nlm.nih.gov/pubmed/24223645 http://dx.doi.org/10.3892/etm.2013.1293 |
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author | DONG, LEI ZHANG, XIAOPENG YU, CHANGMING YU, TING LIU, SHULING HOU, LIHUA FU, LING YI, SHAOQIONG CHEN, WEI |
author_facet | DONG, LEI ZHANG, XIAOPENG YU, CHANGMING YU, TING LIU, SHULING HOU, LIHUA FU, LING YI, SHAOQIONG CHEN, WEI |
author_sort | DONG, LEI |
collection | PubMed |
description | The aim of this study was to establish a tumor model in mice with the expression of luciferase (Luc) and human prostate stem cell antigen (PSCA), in order to evaluate the activities of anticancer drugs or vaccines for prostate cancer. RM-1 cells were stably transfected with pcDNA-Luc and pcDNA-PSCA plasmids. The Luc-expressing cells were examined using a luminometer and the PSCA-expressing cells were examined using a reverse transcription-polymerase chain reaction (RT-PCR) and flow cytometric analysis. Male C57BL/6 mice were inoculated subcutaneously with the RM-PSCA/Luc cells, prior to the tumor growth and survival time of the mice being measured, respectively. In vivo bioluminescence imaging was used to detect Luc expression and immunohistochemical analysis was used to detect PSCA expression. Inoculation of the tumor cells into the C57BL/6 mice closely mimicked the tumor growth of prostate cancer. All of the inoculated mice exhibited a detectable tumor within two weeks. Tumor progression was able to be quantitatively monitored following the inoculation of 1×10(6) RM-PSCA/Luc cells. There was an excellent correlation (R(2)=0.9849) between the photon counts and tumor volume. The expression of PSCA in tumor tissues was confirmed using immunohistochemical analysis. The Luc and PSCA co-expression tumor model was successfully established in mice, which is likely to accelerate the understanding of the pathogenesis of prostate cancer and facilitate the development of novel antitumor drugs or vaccines for the disease. |
format | Online Article Text |
id | pubmed-3820663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-38206632013-11-09 Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model DONG, LEI ZHANG, XIAOPENG YU, CHANGMING YU, TING LIU, SHULING HOU, LIHUA FU, LING YI, SHAOQIONG CHEN, WEI Exp Ther Med Articles The aim of this study was to establish a tumor model in mice with the expression of luciferase (Luc) and human prostate stem cell antigen (PSCA), in order to evaluate the activities of anticancer drugs or vaccines for prostate cancer. RM-1 cells were stably transfected with pcDNA-Luc and pcDNA-PSCA plasmids. The Luc-expressing cells were examined using a luminometer and the PSCA-expressing cells were examined using a reverse transcription-polymerase chain reaction (RT-PCR) and flow cytometric analysis. Male C57BL/6 mice were inoculated subcutaneously with the RM-PSCA/Luc cells, prior to the tumor growth and survival time of the mice being measured, respectively. In vivo bioluminescence imaging was used to detect Luc expression and immunohistochemical analysis was used to detect PSCA expression. Inoculation of the tumor cells into the C57BL/6 mice closely mimicked the tumor growth of prostate cancer. All of the inoculated mice exhibited a detectable tumor within two weeks. Tumor progression was able to be quantitatively monitored following the inoculation of 1×10(6) RM-PSCA/Luc cells. There was an excellent correlation (R(2)=0.9849) between the photon counts and tumor volume. The expression of PSCA in tumor tissues was confirmed using immunohistochemical analysis. The Luc and PSCA co-expression tumor model was successfully established in mice, which is likely to accelerate the understanding of the pathogenesis of prostate cancer and facilitate the development of novel antitumor drugs or vaccines for the disease. D.A. Spandidos 2013-11 2013-09-13 /pmc/articles/PMC3820663/ /pubmed/24223645 http://dx.doi.org/10.3892/etm.2013.1293 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles DONG, LEI ZHANG, XIAOPENG YU, CHANGMING YU, TING LIU, SHULING HOU, LIHUA FU, LING YI, SHAOQIONG CHEN, WEI Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title | Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title_full | Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title_fullStr | Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title_full_unstemmed | Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title_short | Monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
title_sort | monitoring luciferase-labeled human prostate stem cell antigen-expressing tumor growth in a mouse model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820663/ https://www.ncbi.nlm.nih.gov/pubmed/24223645 http://dx.doi.org/10.3892/etm.2013.1293 |
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