MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)

<p>Abstract</p> <p>Background</p> <p>The current method to determine the efficacy of chemoprevention in TRAMP mouse model of carcinoma of prostate (CaP) is by extracting and weighing the prostate at different time points or by immunohistochemistry analysis. Non-invasive...

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Main Authors: Arbab Ali S, Shankar Adarsh, Varma Nadimpalli RS, Deeb Dorrah, Gao Xiaohua, Iskander ASM, Janic Branislava, Ali Meser M, Gautam Subhash C
Format: Article
Language:English
Published: BMC 2011-12-01
Series:BMC Medical Imaging
Online Access:http://www.biomedcentral.com/1471-2342/11/21
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spelling doaj-9eb5ed4b1c3c471fac3bb4108e1af6212020-11-24T21:37:57ZengBMCBMC Medical Imaging1471-23422011-12-011112110.1186/1471-2342-11-21MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)Arbab Ali SShankar AdarshVarma Nadimpalli RSDeeb DorrahGao XiaohuaIskander ASMJanic BranislavaAli Meser MGautam Subhash C<p>Abstract</p> <p>Background</p> <p>The current method to determine the efficacy of chemoprevention in TRAMP mouse model of carcinoma of prostate (CaP) is by extracting and weighing the prostate at different time points or by immunohistochemistry analysis. Non-invasive determination of volumes of prostate glands and seminal vesicles before, during and after treatment would be valuable in investigating the efficacy of newer chemopreventive agents in CaP. The purpose of this study was to determine whether <it>in vivo </it>magnetic resonance imaging (MRI) using a 3 tesla clinical MRI system can be used to follow the effect of chemoprevention in TRAMP model of mouse CaP.</p> <p>Methods</p> <p>Mice were randomized into control and treated groups. The animals in treated group received 10 µmol/kg of CDDO, 5 days a week for 20 weeks. Animals underwent <it>in vivo </it>MRI of prostate gland and seminal vesicles by a clinical 3 Tesla MRI system just before (at 5 weeks), during and at the end of treatment, at 25 weeks. T1-weighted and fat saturation (FATSAT) multiecho fast spin echo T2- weighted images (T2WI) were acquired. Volume of the prostate glands and seminal vesicles was determined from MR images. T2 signal intensity changes in the seminal vesicles were determined by subtracting higher echo time (TE) from lower TE T2WI. Following treatments all animals were sacrificed, prostate and seminal vesicles collected, and the tissues prepared for histological staining. All data were expressed as mean ± 1 standard deviation. Two-way or multivariate analysis of variance followed by post-hoc test was applied to determine the significant differences. A p-value of <0.05 was considered significant.</p> <p>Results</p> <p>Histological analysis indicated tumor in 100% of control mice, whereas 10% of the treated mice showed tumor in prostate gland. Both MRI and measured prostate weights showed higher volume/weight in control mouse group. MRI showed significantly higher volume of seminal vesicles in control animals and T2 signal intensity changes in seminal vesicles of control mice indicating higher number of tumor foci, which was also proven by histology.</p> <p>Conclusions</p> <p><it>In vivo </it>MRI is helpful in determining the efficacy of chemoprevention of prostate cancer in TRAMP mice.</p> http://www.biomedcentral.com/1471-2342/11/21
collection DOAJ
language English
format Article
sources DOAJ
author Arbab Ali S
Shankar Adarsh
Varma Nadimpalli RS
Deeb Dorrah
Gao Xiaohua
Iskander ASM
Janic Branislava
Ali Meser M
Gautam Subhash C
spellingShingle Arbab Ali S
Shankar Adarsh
Varma Nadimpalli RS
Deeb Dorrah
Gao Xiaohua
Iskander ASM
Janic Branislava
Ali Meser M
Gautam Subhash C
MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
BMC Medical Imaging
author_facet Arbab Ali S
Shankar Adarsh
Varma Nadimpalli RS
Deeb Dorrah
Gao Xiaohua
Iskander ASM
Janic Branislava
Ali Meser M
Gautam Subhash C
author_sort Arbab Ali S
title MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
title_short MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
title_full MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
title_fullStr MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
title_full_unstemmed MRI to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (TRAMP)
title_sort mri to assess chemoprevention in transgenic adenocarcinoma of mouse prostate (tramp)
publisher BMC
series BMC Medical Imaging
issn 1471-2342
publishDate 2011-12-01
description <p>Abstract</p> <p>Background</p> <p>The current method to determine the efficacy of chemoprevention in TRAMP mouse model of carcinoma of prostate (CaP) is by extracting and weighing the prostate at different time points or by immunohistochemistry analysis. Non-invasive determination of volumes of prostate glands and seminal vesicles before, during and after treatment would be valuable in investigating the efficacy of newer chemopreventive agents in CaP. The purpose of this study was to determine whether <it>in vivo </it>magnetic resonance imaging (MRI) using a 3 tesla clinical MRI system can be used to follow the effect of chemoprevention in TRAMP model of mouse CaP.</p> <p>Methods</p> <p>Mice were randomized into control and treated groups. The animals in treated group received 10 µmol/kg of CDDO, 5 days a week for 20 weeks. Animals underwent <it>in vivo </it>MRI of prostate gland and seminal vesicles by a clinical 3 Tesla MRI system just before (at 5 weeks), during and at the end of treatment, at 25 weeks. T1-weighted and fat saturation (FATSAT) multiecho fast spin echo T2- weighted images (T2WI) were acquired. Volume of the prostate glands and seminal vesicles was determined from MR images. T2 signal intensity changes in the seminal vesicles were determined by subtracting higher echo time (TE) from lower TE T2WI. Following treatments all animals were sacrificed, prostate and seminal vesicles collected, and the tissues prepared for histological staining. All data were expressed as mean ± 1 standard deviation. Two-way or multivariate analysis of variance followed by post-hoc test was applied to determine the significant differences. A p-value of <0.05 was considered significant.</p> <p>Results</p> <p>Histological analysis indicated tumor in 100% of control mice, whereas 10% of the treated mice showed tumor in prostate gland. Both MRI and measured prostate weights showed higher volume/weight in control mouse group. MRI showed significantly higher volume of seminal vesicles in control animals and T2 signal intensity changes in seminal vesicles of control mice indicating higher number of tumor foci, which was also proven by histology.</p> <p>Conclusions</p> <p><it>In vivo </it>MRI is helpful in determining the efficacy of chemoprevention of prostate cancer in TRAMP mice.</p>
url http://www.biomedcentral.com/1471-2342/11/21
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