3-D Longitudinal Imaging of Tumor Angiogenesis in Mice in Vivo Using Ultrafast Doppler Tomography

TL;DR

This paper demonstrates the use of ultrafast Doppler tomography for non-invasive, high-resolution 3D imaging of tumor angiogenesis in mice, providing structural and functional insights into vascular development during tumor growth.

Contribution

The study extends ultrafast Doppler to 3D imaging of tumor vasculature in vivo, offering detailed quantitative analysis and comparison with other imaging techniques.

Findings

Tumor vasculature originates from pre-existing vessels and expands until a critical size.

Vessel diameter distribution remains relatively constant during tumor growth.

Vascularization correlates more with tumor radius than volume.

Abstract

Angiogenesis, the formation of new vessels, is one of the key mechanisms in tumor development and an appealing target for therapy. Non-invasive, high-resolution, high sensitivity, quantitative 3D imaging techniques are required to correctly depict tumor heterogeneous vasculature over time. Ultrafast Doppler was recently introduced and provides an unprecedented combination of resolution, penetration depth and sensitivity without requiring any contrast agents. The technique was further extended to 3D with Ultrafast Doppler Tomography (UFD-T). In this work, UFD-T was applied to the monitoring of tumor angiogenesis in vivo providing structural and functional information at different stages of development. UFD-T volume renderings showed that our murine model's vasculature stems from pre-existing vessels and sprouts to perfuse the whole volume as the tumor grows until a critical size is reached. Then, as the network becomes insufficient, the tumor core is no longer irrigated because the vasculature is mainly concentrated in the periphery. In addition to spatial distribution and growth patterns, UFD-T allowed a quantitative analysis of vessel size and length, revealing that the diameter-distribution of vessels remained relatively constant throughout tumor growth. The network is dominated by small vessels at all stages of tumor development with more than 74% of the vessels less than 200 $\mu$m in diameter. This study also showed that cumulative vessel length is more closely related to tumor radius than volume, indicating that the vascularization becomes insufficient when a critical mass is reached. UFD-T was also compared with dynamic contrast-enhanced ultrasound (DCE-US) and shown to provide complementary information regarding the link between structure and perfusion. In conclusion, UFD-T is capable of an in vivo quantitative assessment of the development of tumor vasculature (vessels with blood speed >1mm/s (sensitivity limit) assessed with a resolution limit of 80 $\mu$m) in 3D. The technique has very interesting potential as a tool for treatment monitoring, response assessment and treatment planning for optimal drug efficiency.