Literature DB >> 22741041

In Vivo Magnetic Resonance Imaging for Investigating the Development and Distribution of Experimental Brain Metastases due to Breast Cancer.

Mevan Perera1, Emeline J Ribot, Dean B Percy, Catherine McFadden, Carmen Simedrea, Diane Palmieri, Ann F Chambers, Paula J Foster.   

Abstract

INTRODUCTION: The overall goal of this study was to assess the utility of three-dimensional magnetic resonance imaging (MRI) for monitoring the temporal and spatial development of experimental brain metastasis in mice.
MATERIALS AND METHODS: Brain metastatic human breast cancer cells (231-BR or 231-BR-HER2) were injected intracardially in nude mice for delivery to the brain. Mouse brains were imaged in vivo at different time points using a balanced steady-state-free precession (bSSFP) pulse sequence at 1.5 T. Brains were categorized into four regions: cortex, central brain, olfactory, and posterior. The number of metastases and their volumes were quantified for both cell lines.
RESULTS: There was no difference in the mean number of metastases for either cell line. The volumes of metastases in mice injected with 231-BR-HER2 cells were significantly larger than those for mice injected with 231-BR cells. The growth rate for 231-BR-HER2 metastases was 67.5% compared with 54.4% for the 231-BR metastases. More than 50% of metastases were located in the cortex and 25% to 30% of metastases were identified in the central brain for each time point and for mice injected with either cell line. The volumes of metastases were significantly larger in mice with fewer metastases at end point. SIGNIFICANT
CONCLUSIONS: MRI provided a comprehensive accounting of the number and size of experimental brain metastases in the whole mouse brain at multiple time points. This approach has provided new information about the temporal and spatial development of metastases in the brain not possible by other histopathologic or imaging methods.

Entities:  

Year:  2012        PMID: 22741041      PMCID: PMC3384276          DOI: 10.1593/tlo.12109

Source DB:  PubMed          Journal:  Transl Oncol        ISSN: 1936-5233            Impact factor:   4.243


  35 in total

Review 1.  CNS metastases in breast cancer.

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2.  Breast cancers with brain metastases are more likely to be estrogen receptor negative, express the basal cytokeratin CK5/6, and overexpress HER2 or EGFR.

Authors:  David G Hicks; Sarah M Short; Nichole L Prescott; Shannon M Tarr; Kara A Coleman; Brian J Yoder; Joseph P Crowe; Toni K Choueiri; Andrea E Dawson; G Thomas Budd; Raymond R Tubbs; Graham Casey; Robert J Weil
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3.  Quantitative analysis of breast cancer tissue microarrays shows that both high and normal levels of HER2 expression are associated with poor outcome.

Authors:  Robert L Camp; Marisa Dolled-Filhart; Bonnie L King; David L Rimm
Journal:  Cancer Res       Date:  2003-04-01       Impact factor: 12.701

4.  Predilection of brain metastasis in gray and white matter junction and vascular border zones.

Authors:  T L Hwang; T P Close; J M Grego; W L Brannon; F Gonzales
Journal:  Cancer       Date:  1996-04-15       Impact factor: 6.860

5.  The natural history of breast cancer patients with brain metastases.

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6.  Expression of vascular endothelial growth factor is necessary but not sufficient for production and growth of brain metastasis.

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7.  In vivo single scan detection of both iron-labeled cells and breast cancer metastases in the mouse brain using balanced steady-state free precession imaging at 1.5 T.

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10.  In vivo characterization of changing blood-tumor barrier permeability in a mouse model of breast cancer metastasis: a complementary magnetic resonance imaging approach.

Authors:  Dean B Percy; Emeline J Ribot; Yuhua Chen; Catherine McFadden; Carmen Simedrea; Patricia S Steeg; Ann F Chambers; Paula J Foster
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4.  Characterization of passive permeability at the blood-tumor barrier in five preclinical models of brain metastases of breast cancer.

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Review 6.  Brain metastases from breast cancer: lessons from experimental magnetic resonance imaging studies and clinical implications.

Authors:  Donna H Murrell; Paula J Foster; Ann F Chambers
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7.  Water Selective Imaging and bSSFP Banding Artifact Correction in Humans and Small Animals at 3T and 7T, Respectively.

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9.  Targeting CXCR1 on breast cancer stem cells: signaling pathways and clinical application modelling.

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10.  Multimodal evaluation of hypoxia in brain metastases of lung cancer and interest of hypoxia image-guided radiotherapy.

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Journal:  Sci Rep       Date:  2021-05-27       Impact factor: 4.379

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