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3-D Ultrasound Localization Microscopy for Identifying Microvascular Morphology Features of Tumor Angiogenesis at a Resolution Beyond the Diffraction Limit of Conventional Ultrasound

机译:3-D超声定位显微镜用于以超出常规超声衍射极限的分辨率识别肿瘤血管生成的微血管形态特征

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摘要

Angiogenesis has been known as a hallmark of solid tumor cancers for decades, yet ultrasound has been limited in its ability to detect the microvascular changes associated with malignancy. Here, we demonstrate the potential of 'ultrasound localization microscopy' applied volumetrically in combination with quantitative analysis of microvascular morphology, as an approach to overcome this limitation. This pilot study demonstrates our ability to image complex microvascular patterns associated with tumor angiogenesis in-vivo at a resolution of tens of microns - substantially better than the diffraction limit of traditional clinical ultrasound, yet using an 8 MHz clinical ultrasound probe. Furthermore, it is observed that data from healthy and tumor-bearing tissue exhibit significant differences in microvascular pattern and density. Results suggests that with continued development of these novel technologies, ultrasound has the potential to detect biomarkers of cancer based on the microvascular 'fingerprint' of malignant angiogenesis rather than through imaging of blood flow dynamics or the tumor mass itself.
机译:数十年来,血管生成一直被认为是实体瘤癌症的标志,然而超声在检测与恶性肿瘤相关的微血管变化方面的能力受到限制。在这里,我们证明了“超声定位显微镜”在体积上与定量分析微血管形态相结合的潜力,以此作为克服这一局限性的一种方法。这项先导研究证明了我们能够以数十微米的分辨率在体内成像与肿瘤血管生成相关的复杂微血管模式的能力-显着优于传统临床超声的衍射极限,但仍使用8 MHz临床超声探头。此外,可以观察到,来自健康组织和肿瘤组织的数据在微血管形态和密度方面显示出显着差异。结果表明,随着这些新技术的不断发展,超声技术有可能根据恶性血管生成的微血管“指纹”而不是通过对血流动力学或肿瘤本身成像,来检测癌症的生物标志物。

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