Optical imaging of the peri-tumoral inflammatory response in breast cancer

Peri-tumoral inflammation is a common tumor response that plays a central role in tumor invasion and metastasis, and inflammatory cell recruitment is essential to this process. The purpose of this study was to determine whether injected fluorescently-labeled monocytes accumulate within murine breast...

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Published inJournal of translational medicine Vol. 7; no. 1; p. 94
Main Authors Sista, Akhilesh K, Knebel, Robert J, Tavri, Sidhartha, Johansson, Magnus, DeNardo, David G, Boddington, Sophie E, Kishore, Sirish A, Ansari, Celina, Reinhart, Verena, Coakley, Fergus V, Coussens, Lisa M, Daldrup-Link, Heike E
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 11.11.2009
BioMed Central
BMC
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Summary:Peri-tumoral inflammation is a common tumor response that plays a central role in tumor invasion and metastasis, and inflammatory cell recruitment is essential to this process. The purpose of this study was to determine whether injected fluorescently-labeled monocytes accumulate within murine breast tumors and are visible with optical imaging. Murine monocytes were labeled with the fluorescent dye DiD and subsequently injected intravenously into 6 transgenic MMTV-PymT tumor-bearing mice and 6 FVB/n control mice without tumors. Optical imaging (OI) was performed before and after cell injection. Ratios of post-injection to pre-injection fluorescent signal intensity of the tumors (MMTV-PymT mice) and mammary tissue (FVB/n controls) were calculated and statistically compared. MMTV-PymT breast tumors had an average post/pre signal intensity ratio of 1.8+/- 0.2 (range 1.1-2.7). Control mammary tissue had an average post/pre signal intensity ratio of 1.1 +/- 0.1 (range, 0.4 to 1.4). The p-value for the difference between the ratios was less than 0.05. Confocal fluorescence microscopy confirmed the presence of DiD-labeled cells within the breast tumors. Murine monocytes accumulate at the site of breast cancer development in this transgenic model, providing evidence that peri-tumoral inflammatory cell recruitment can be evaluated non-invasively using optical imaging.
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ISSN:1479-5876
1479-5876
DOI:10.1186/1479-5876-7-94