Application of scanning acoustic microscopy for evaluation of MMP activation in multiple cancer cell lines with a

Hasan Ozan Otaş1, Nasire Uluç2,3, İrem Demirkan2,4

  • 1Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Boğaziçi University, İstanbul, Turkey.

Abstract

Insights

Scanning acoustic microscopy (SAM) with an activatable probe effectively detected matrix metalloproteinase (MMP) activity in HT1080 cancer cells. This novel approach offers a new way to study MMP roles in cancer progression.

Area of Science:

  • Biophysics
  • Molecular Biology
  • Cancer Research

Background:

  • Matrix metalloproteinases (MMPs) are crucial in cancer progression, but their detection is challenging.
  • Further assays are needed to understand MMPs' fundamental roles in pathophysiology.
  • This study explores a novel method for visualizing MMP activity.

Purpose of the Study:

  • To evaluate the use of an activatable probe with scanning acoustic microscopy (SAM) for visualizing in vitro matrix metalloproteinase (MMP) activity.
  • To determine if SAM can acoustically detect MMP activity in cell line models.

Main Methods:

  • Scanning acoustic impedance microscopy was used to create acoustic impedance maps of HT1080, THP-1, and SK-MEL-28 cell lines.
  • Cells were incubated with or without the MMPSense 680 probe.
  • Confocal laser scanning microscopy was used for visual validation, and cell viability assays were performed to rule out artifacts.

Main Results:

  • This is the first study demonstrating SAM's applicability for acoustically evaluating MMPSense 680 probe cleavage in a cellular medium.
  • SAM measurements with the activatable probe effectively detected MMPSense 680 probe cleavage in the HT1080 human fibrosarcoma cell line.
  • Acoustic impedance measurements revealed variations in MMP activity.

Conclusions:

  • Scanning acoustic microscopy (SAM) combined with the MMPSense 680 smart probe can detect proteolytic activity in vitro.
  • SAM offers a novel alternative tool for studying MMP roles in cancer progression prior to clinical applications.
  • This method provides a new way to understand MMPs' impact on cancer pathophysiology.