Nanosecond pulsed electric fields impair viability and mucin expression in mucinous colorectal carcinoma cell

Bioelectrochemistry. 2021 Oct:141:107844. doi: 10.1016/j.bioelechem.2021.107844. Epub 2021 May 20.

Abstract

Nanosecond pulsed electric fields (nsPEFs) are a non-thermal technology that can induce a myriad of biological responses and changes in cellular physiology. nsPEFs have gained significant attention as a novel cancer therapy. However, studies investigating the application of nsPEF in mucinous carcinomas are scarce. In this study, we explored several biological responses in two mucinous colorectal adenocarcinoma cell lines, LS 174T and HT-29, to nsPEF treatment. We determined the overall cell survival and viability rates following nsPEF treatment using CCK-8 and colony formation assays. We measured the intracellular effects of nsPEF treatment by analyzing cell cycle distribution, cell apoptosis and mitochondrial potential. We also analyzed mucin production at both mRNA and protein levels. Our results showed that nsPEF treatment significantly reduced mucinous cell viability in a dose-dependent manner. nsPEF treatment increased cell cycles arrest at G0/G1 while the proportion of G2/M cells gradually decreased. Cell apoptosis increased following nsPEF treatment with a clear loss in mitochondrial membrane potential. Furthermore, the protein expression of functional mucin family members decreased after nsPEF treatment. In conclusion, nsPEF treatment reduced MCRC cell viability, cell proliferation, and mucin protein production while promoted apoptosis. Our work is a pilot study that projects some insights into the potential clinical applications of nsPEFs in treating mucinous colorectal carcinoma.

Keywords: Cell apoptosis; Mucin expression; Mucinous colorectal cancer; nsPEF.

MeSH terms

  • Apoptosis
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Survival
  • Cholecystokinin / metabolism
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Electricity*
  • Humans
  • Membrane Potential, Mitochondrial
  • Mucins / metabolism*
  • Peptide Fragments / metabolism

Substances

  • Mucins
  • Peptide Fragments
  • cholecystokinin 8
  • Cholecystokinin