Methods for detecting host genetic modifiers of tumor vascular function using dynamic near-infrared fluorescence imaging

被引:17
|
作者
Jagtap, Jaidip [1 ]
Sharma, Gayatri [1 ]
Parchur, Abdul K. [1 ]
Gogineni, Venkateswara [2 ]
Bergom, Carmen [3 ]
White, Sarah [2 ]
Flister, Michael J. [4 ]
Joshi, Amit [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Biomed Engn, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Radiol, 8700 W Wisconsin Ave, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Physiol, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2018年 / 9卷 / 02期
关键词
PRINCIPAL COMPONENT ANALYSIS; INDOCYANINE GREEN; BREAST-CANCER; CONTRAST; PHARMACOKINETICS; SPECTROSCOPY; TOMOGRAPHY; WINDOW; ICG;
D O I
10.1364/BOE.9.000543
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Vascular supply is a critical component of the tumor microenvironment (TME) and is essential for tumor growth and metastasis, yet the endogenous genetic modifiers that impact vascular function in the TME are largely unknown. To identify the host TME modifiers of tumor vascular function, we combined a novel genetic mapping strategy [Consomic Xenograft Model] with near-infrared (NIR) fluorescence imaging and multiparametric analysis of pharmacokinetic modeling. To detect vascular flow, an intensified cooled camera based dynamic NIR imaging system with 785 nm laser diode based excitation was used to image the whole-body fluorescence emission of intravenously injected indocyanine green dye. Principal component analysis was used to extract the spatial segmentation information for the lungs, liver, and tumor regions-of-interest. Vascular function was then quantified by pK modeling of the imaging data, which revealed significantly altered tissue perfusion and vascular permeability that were caused by host genetic modifiers in the TME. Collectively, these data demonstrate that NIR fluorescent imaging can be used as a non-invasive means for characterizing host TME modifiers of vascular function that have been linked with tumor risk, progression, and response to therapy. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:543 / 556
页数:14
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