A multiparametric fluorescent visualization approach for detecting drug resistance in living cancer cells

Talanta. 2023 Jul 1:259:124564. doi: 10.1016/j.talanta.2023.124564. Epub 2023 Apr 16.

Abstract

Drug resistance is a worldwide health care crisis which impedes disease treatment and increases financial burden, especially for its multifactorial nature and high complexity. Herein, we developed a multiparametric approach to visualize and detect drug resistance in living cancer cells, through the combination of DNA-templated covalent protein labeling strategy and fluorescent resonance energy transfer technique. Gefitinib resistance in non-small cell lung cancer caused by mesenchymal-epidermal transition factor (Met) overexpression and hyperactivation was investigated as a proof-of-concept. Unlike the traditional single-factor investigation, the proposed approach evaluated the contribution of three important parameters towards the resistance, including the changes of Met expression level, the homodimerization of Met with itself and the heterodimerization of Met with epidermal growth factor receptor (EGFR). A multiple regression model based on these three parameters was tentatively established for evaluation of the resistance level of laboratory-developed resistant cells and evaluation of the resistance level of patient-derived cells. Such an approach facilitates a quick identification of a drug resistance, to evaluate not only the resistance level but also the resistance mechanism.

Keywords: Fluorescence resonance energy transfer; Gefitinib resistance; Multiparametric detection; Protein dimerization; Protein hyperactivation.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / metabolism
  • Mutation
  • Protein Kinase Inhibitors / pharmacology
  • Quinazolines / therapeutic use
  • Signal Transduction

Substances

  • Quinazolines
  • Protein Kinase Inhibitors
  • Antineoplastic Agents