Intravital imaging and cavitation monitoring of antivascular ultrasound in tumor microvasculature

TL;DR

This study uses intravital microscopy and acoustic monitoring to understand how antivascular ultrasound causes blood vessel damage in tumors, revealing vessel type, size, and cavitation signatures linked to vascular effects.

Contribution

It introduces an integrated intravital imaging and acoustic monitoring platform to elucidate mechanisms of antivascular ultrasound in tumor microvasculature.

Findings

Vascular damage occurs mainly in tumor-affected, smaller vessels.

Higher pressure increases severity of vascular disruption.

Distinct cavitation signatures correlate with vascular effects.

Abstract

Focused ultrasound stimulated microbubbles have been shown to be capable of inducing blood flow shutdown and necrosis in a range of tissue types in an approach termed antivascular ultrasound or mechanical ablation. In oncology, this approach has demonstrated tumor growth inhibition, and profound synergistic antitumor effects when combined with traditional platforms of chemo, radiation and immune therapies. However, the exposure schemes employed have been broad and underlying mechanisms remain unclear with fundamental questions about exposures, vessel types and sizes involved, and the nature of bubble behaviors and their acoustic emissions resulting in vascular damage, impeding the establishment of standard protocols. Here, ultrasound transmitters and receivers are integrated into a murine dorsal window chamber tumor model for intravital microscopy studies capable of real time visual and acoustic monitoring during antivascular ultrasound. Vessel type (normal and tumor affected), caliber, and viability are assessed under higher pressure conditions (1, 2, and 3 MPa), and cavitation signatures are linked to the biological effects. Vascular events occurred preferentially in tumor affected vessels with greater incidence in smaller vessels and with more severity as a function of increasing pressure. Vascular blood flow shutdown was found to be due to a combination of focal disruption events and network related flow changes. Acoustic emissions displayed elevated broadband noise and distinct sub and ultra harmonics and their associated third order peaks with increasing pressure. The observed vascular events taken collectively with identified cavitation signatures provide an improved mechanistic understanding of antivascular ultrasound at the microscale, with implications for establishing a specific treatment protocol and control platform.