Evaluating the effects of radiation and acoustically-stimulated microbubble therapy in an in vivo breast cancer model.
Deepa SharmaChristine M TarapackiHarini KandavelMailoan PanchalingamHyunjung Christina KimHolliday CartarAhmed El KaffasGregory J CzarnotaPublished in: PloS one (2023)
Ultrasound-stimulated microbubbles (USMB) cause localized vascular effects and sensitize tumors to radiation therapy (XRT). We investigated acoustic parameter optimization for combining USMB and XRT. We treated breast cancer xenograft tumors with 500 kHz pulsed ultrasound at varying pressures (570 or 740 kPa), durations (1 to 10 minutes), and microbubble concentrations (0.01 to 1% (v/v)). Radiation therapy (2 Gy) was administered immediately or after a 6-hour delay. Histological staining of tumors 24 hours after treatment detected changes in cell morphology, cell death, and microvascular density. Significant cell death resulted at 570 kPa after a 1-minute exposure with 1% (v/v) microbubbles with or without XRT. However, significant microvascular disruption required higher ultrasound pressure and exposure duration greater than 5 minutes. Introducing a 6-hour delay between treatments (USMB and XRT) showed a similar tumor effect with no further improvement in response as compared to when XRT was delivered immediately after USMB.
Keyphrases
- cell death
- radiation therapy
- magnetic resonance imaging
- blood pressure
- contrast enhanced ultrasound
- radiation induced
- ultrasound guided
- single cell
- cell cycle arrest
- cell therapy
- high frequency
- stem cells
- squamous cell carcinoma
- atomic force microscopy
- computed tomography
- mesenchymal stem cells
- bone marrow
- young adults
- breast cancer risk