AI Article Synopsis

  • Low frequency ultrasound (20 to 60 kHz) can selectively kill cancer cells (neoplastic cells) through a technique known as sonodynamic therapy (SDT), especially when paired with special agents called sonosensitizers.
  • The study demonstrates a reliable method for generating and applying this ultrasound in lab settings to ensure consistent cell destruction, which is important for testing potential therapies.
  • The research also explores how agents that deplete cholesterol and affect the cell's structure could enhance the sensitivity of cancer cells to ultrasound, paving the way for more effective treatments.

Article Abstract

Low frequency ultrasound in the 20 to 60 kHz range is a novel physical modality by which to induce selective cell lysis and death in neoplastic cells. In addition, this method can be used in combination with specialized agents known as sonosensitizers to increase the extent of preferential damage exerted by ultrasound against neoplastic cells, an approach referred to as sonodynamic therapy (SDT). The methodology for generating and applying low frequency ultrasound in a preclinical in vitro setting is presented to demonstrate that reproducible cell destruction can be attained in order to examine and compare the effects of sonication on neoplastic and normal cells. This offers a means by which to reliably sonicate neoplastic cells at a level of consistency required for preclinical therapeutic assessment. In addition, the effects of cholesterol-depleting and cytoskeletal-directed agents on potentiating ultrasonic sensitivity in neoplastic cells are discussed in order to elaborate on mechanisms of action conducive to sonochemotherapeutic approaches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545152PMC
http://dx.doi.org/10.3791/53060DOI Listing

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