PO.PR02.02 · 预防研究
剪切波弹性成像与光声成像无创识别肿瘤微环境中的耐药区域
Shear wave elastography and photoacoustic imaging to non-invasively identify resistant regions in the tumor microenvironment
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摘要 Abstract
中文摘要
硬度增加是恶性肿瘤的一个标志,并可因间质压升高而阻碍化疗药物递送。临床上使用剪切波弹性成像(SWE)评估肿瘤硬度;然而,将SWE与解剖、功能和分子信息相结合的小动物成像系统一直缺乏。在此,我们首次提出将采用超快平面波采集的高频超声与毛细血管功能和肿瘤氧合评估相结合,为肿瘤微环境提供无创、详细的洞察。将CT26小鼠结直肠癌细胞皮下植入Balb/C小鼠胁部以建立实体瘤。两周后,使用Vevo® F2 LAZR-X系统进行肿瘤成像。在单次成像过程中,在不移动动物的情况下评估肿瘤结构、血管化(静脉注射MicroMarker造影剂后)、氧合/缺氧(通过光声成像)和硬度(通过SWE)。氧激发试验识别出对条件变化有响应的区域(潜在可治疗的“响应者”区域),并将其与SWE测量的硬度和血管数据进行比较。我们的结果表明,将SWE与超声和光声成像相结合可提供对肿瘤微环境的实时、无创洞察。由SWE识别的高硬度区域与间质压升高相关,这可能限制药物递送并影响治疗疗效。通过将血管和缺氧特征与硬度一同绘制,这种多模态方法揭示了肿瘤内和肿瘤间的异质性。硬度较高的区域与氧无响应区域和较低的血管密度相关,为不断演变的肿瘤特征提供了一种无创表征。本研究确立了SWE作为无创评估肿瘤硬度及其与缺氧和血管化关系的有力工具。将SWE与光声和超声成像相结合,提供了一种全面、多维的方法来表征肿瘤微环境,超越了仅基于肿瘤体积的传统测量。这一进展增进了对肿瘤异质性的理解,并支持个体化治疗策略的开发,最终改善治疗规划和结局。
查看英文原文 English abstract
Increased stiffness is a hallmark of malignant tumors and can impede chemotherapy delivery due to elevated interstitial pressure. Clinically, tumor stiffness is assessed using Shear Wave Elastography (SWE); however, small animal imaging systems combining SWE with anatomical, functional, and molecular information have been lacking. Here, we present, for the first time, high-frequency ultrasound with ultrafast plane wave acquisition combined with assessments of capillary function and tumor oxygenation, offering non-invasive, detailed insight into the tumor microenvironment.CT26 murine colorectal carcinoma cells were implanted subcutaneously into the flanks of Balb/C mice to establish solid tumors. Two weeks later, tumor imaging was performed using the Vevo® F2 LAZR-X system. During a single imaging session, tumor structure, vascularization (after intravenous injection of the MicroMarker contrast agent), oxygenation/hypoxia (via photoacoustic imaging), and stiffness (via SWE) were evaluated without moving the animals. An oxygen challenge identified regions responsive to changing conditions (potentially treatable “responder” regions), which were compared with SWE-measured stiffness and vascular data.Our results demonstrate that combining SWE with ultrasound and photoacoustic imaging provides real-time, non-invasive insights into the tumor microenvironment. Regions of high stiffness, identified by SWE, are linked to increased interstitial pressure, which may restrict drug delivery and affect treatment efficacy. By mapping vascular and hypoxic features alongside stiffness, this multimodal approach revealed intra- and inter-tumor heterogeneity. Areas with higher stiffness correlated with non-responsive oxygen regions and lower vascular density, providing a non-invasive representation of evolving tumor characteristics.This study establishes SWE as a powerful tool for non-invasively assessing tumor stiffness and its relationship with hypoxia and vascularity. Integrating SWE with photoacoustic and ultrasound imaging provides a comprehensive, multidimensional method to characterize the tumor microenvironment, moving beyond traditional measures based solely on tumor volume. This advancement enhances understanding of tumor heterogeneity and supports the development of personalized therapeutic strategies, ultimately improving treatment planning and outcomes
利益披露 Disclosure
S. K. Burris,
FUJIFILM VisualSonics Inc. Employment.
C. O'Riordan,
FUJIFILM VisualSonics Inc. Employment.
P. Kesa,
FUJIFILM VisualSonics Inc. Employment.
P. Trochet,
FUJIFILM VisualSonics Inc. Employment.
D. Fuchs,
FUJIFILM VisualSonics Inc. Employment.