An in vivo platform for tumor biomarker assessment.

Tumor biomarkers provide a quantitative tool for following tumor progression and response to therapy. However, investigations of clinically useful tumor biomarkers are time-consuming, costly, and limited by patient and tumor heterogeneity. In addition, assessment of biomarkers as indicators of thera...

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Main Authors: Elliot L Servais, Kei Suzuki, Christos Colovos, Luis Rodriguez, Camelia Sima, Martin Fleisher, Valerie W Rusch, Michel Sadelain, Prasad S Adusumilli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3202552?pdf=render
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spelling doaj-d8cb9ce1093f4d6eaba681074c48e6cd2020-11-25T02:55:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2672210.1371/journal.pone.0026722An in vivo platform for tumor biomarker assessment.Elliot L ServaisKei SuzukiChristos ColovosLuis RodriguezCamelia SimaMartin FleisherValerie W RuschMichel SadelainPrasad S AdusumilliTumor biomarkers provide a quantitative tool for following tumor progression and response to therapy. However, investigations of clinically useful tumor biomarkers are time-consuming, costly, and limited by patient and tumor heterogeneity. In addition, assessment of biomarkers as indicators of therapy response is confounded by the concomitant use of multiple therapeutic interventions. Herein we report our use of a clinically relevant orthotopic animal model of malignant pleural mesothelioma for investigating tumor biomarkers. Utilizing multi-modality imaging with correlative histopathology, we demonstrate the utility and accuracy of the mouse model in investigating tumor biomarkers--serum soluble mesothelin-related peptide (SMRP) and osteopontin (OPN). This model revealed percentage change in SMRP level to be an accurate biomarker of tumor progression and therapeutic response--a finding consistent with recent clinical studies. This in vivo platform demonstrates the advantages of a validated mouse model for the timely and cost-effective acceleration of human biomarker translational research.http://europepmc.org/articles/PMC3202552?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Elliot L Servais
Kei Suzuki
Christos Colovos
Luis Rodriguez
Camelia Sima
Martin Fleisher
Valerie W Rusch
Michel Sadelain
Prasad S Adusumilli
spellingShingle Elliot L Servais
Kei Suzuki
Christos Colovos
Luis Rodriguez
Camelia Sima
Martin Fleisher
Valerie W Rusch
Michel Sadelain
Prasad S Adusumilli
An in vivo platform for tumor biomarker assessment.
PLoS ONE
author_facet Elliot L Servais
Kei Suzuki
Christos Colovos
Luis Rodriguez
Camelia Sima
Martin Fleisher
Valerie W Rusch
Michel Sadelain
Prasad S Adusumilli
author_sort Elliot L Servais
title An in vivo platform for tumor biomarker assessment.
title_short An in vivo platform for tumor biomarker assessment.
title_full An in vivo platform for tumor biomarker assessment.
title_fullStr An in vivo platform for tumor biomarker assessment.
title_full_unstemmed An in vivo platform for tumor biomarker assessment.
title_sort in vivo platform for tumor biomarker assessment.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Tumor biomarkers provide a quantitative tool for following tumor progression and response to therapy. However, investigations of clinically useful tumor biomarkers are time-consuming, costly, and limited by patient and tumor heterogeneity. In addition, assessment of biomarkers as indicators of therapy response is confounded by the concomitant use of multiple therapeutic interventions. Herein we report our use of a clinically relevant orthotopic animal model of malignant pleural mesothelioma for investigating tumor biomarkers. Utilizing multi-modality imaging with correlative histopathology, we demonstrate the utility and accuracy of the mouse model in investigating tumor biomarkers--serum soluble mesothelin-related peptide (SMRP) and osteopontin (OPN). This model revealed percentage change in SMRP level to be an accurate biomarker of tumor progression and therapeutic response--a finding consistent with recent clinical studies. This in vivo platform demonstrates the advantages of a validated mouse model for the timely and cost-effective acceleration of human biomarker translational research.
url http://europepmc.org/articles/PMC3202552?pdf=render
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