Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI

Nick G. Costouros, Dominique Lorang, Yantian Zhang, Marshall S. Miller, Felix E. Diehn, Stephen M. Hewitt, Michael V. Knopp, King C P Li, Peter L. Choyke, H. Richard Alexander, Steven Libutti

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Current methods of studying angiogenesis are limited In their ability to serially evaluate In vivo function throughout a target tissue. Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and pharmacokinetic modeling provide a useful method for evaluating tissue vasculature based on contrast accumulation and washout. While it is often assumed that areas of high contrast enhancement and washout comprise areas of Increased angiogenesis and tumor activity, the actual molecular pathways that are active in such areas are poorly understood. Using DCE-MRI in a murine subcutaneous tumor model, we were able to perform pharmacokinetic functional analysis of a tumor, coregistration of MRI images with histological cross-sections, immunohistochemistry, laser capture microdissection, and genetic profiling of tumor heterogeneity based on pharmacokinetic parameters. Using imaging as a template for biologic investigation, we have not found evidence of increased expression of proangiogenic modulators at the transcriptional level in either distinct pharmacokinetic region. Furthermore, these regions show no difference on histology and CD31 immunohistochemistry. However, the expression of ribosomal proteins was greatly increased in high enhancement and washout regions, implying increased protein translation and consequent increased cellular activity. Together, these findings point to the potential importance of posttranscriptional regulation in angiogenesis and the need for the development of angiogenesis-specific contrast agents to evaluate in vivo angiogenesis at a molecular level.

Original languageEnglish (US)
Pages (from-to)301-308
Number of pages8
JournalMolecular Imaging
Volume1
Issue number3
DOIs
StatePublished - Jul 1 2002

Fingerprint

angiogenesis
Pharmacokinetics
gene expression
Microarrays
Gene expression
Magnetic resonance imaging
Tumors
tumors
fallout
Gene Expression
Magnetic resonance
Imaging techniques
Neoplasms
Microdissection
Immunohistochemistry
Magnetic Resonance Imaging
magnetic resonance
Tissue
Laser Capture Microdissection
Proteins

All Science Journal Classification (ASJC) codes

  • Condensed Matter Physics
  • Molecular Medicine
  • Radiology Nuclear Medicine and imaging
  • Biotechnology
  • Biomedical Engineering

Keywords

  • Gadolinium
  • Gene expression
  • Laser capture microdissection
  • Magnetic resonance imaging
  • Microarray

Cite this

Costouros, Nick G. ; Lorang, Dominique ; Zhang, Yantian ; Miller, Marshall S. ; Diehn, Felix E. ; Hewitt, Stephen M. ; Knopp, Michael V. ; Li, King C P ; Choyke, Peter L. ; Alexander, H. Richard ; Libutti, Steven. / Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI. In: Molecular Imaging. 2002 ; Vol. 1, No. 3. pp. 301-308.
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Costouros, NG, Lorang, D, Zhang, Y, Miller, MS, Diehn, FE, Hewitt, SM, Knopp, MV, Li, KCP, Choyke, PL, Alexander, HR & Libutti, S 2002, 'Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI', Molecular Imaging, vol. 1, no. 3, pp. 301-308. https://doi.org/10.1162/153535002760235481

Microarray gene expression analysis of murine tumor heterogeneity defined by dynamic contrast-enhanced MRI. / Costouros, Nick G.; Lorang, Dominique; Zhang, Yantian; Miller, Marshall S.; Diehn, Felix E.; Hewitt, Stephen M.; Knopp, Michael V.; Li, King C P; Choyke, Peter L.; Alexander, H. Richard; Libutti, Steven.

In: Molecular Imaging, Vol. 1, No. 3, 01.07.2002, p. 301-308.

Research output: Contribution to journalArticle

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AU - Costouros, Nick G.

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AU - Zhang, Yantian

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AU - Hewitt, Stephen M.

AU - Knopp, Michael V.

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AU - Choyke, Peter L.

AU - Alexander, H. Richard

AU - Libutti, Steven

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