Drug resistance in chemotherapy has been greatly challenging
for
cancer treatment. Research has revealed that extracellular vesicles
(EVs) secreted by drug-resistant cells could induce chemoresistance
in susceptible cells. However, there are few ways to give direct evidence
of it. Herein, we have proposed a microchip-based system to study
the drug resistance of a wild-type human lung adenocarcinoma cell
line (A549/WT) induced by EVs derived from A549/DDP cells that are
resistant to cisplatin (DDP) inherently. EVs derived from A549/DDP
were proved to be the crucial factor that enhanced the resistance
of A549/WT to DDP through live and dead cell staining, cell viability
testing, and immunofluorescence of P-glycoprotein in the off-chip
assay. Then, it was further validated that drug resistance of A549/WT
cells to DDP significantly increased after being cocultured with A549/DDP
cells within 96 h in the on-chip assay. These findings proved that
the change of A549/WT drug resistance was caused by intercellular
interaction, which was mainly mediated by EVs. In addition, we successfully
reversed the EV-induced drug resistance of A549/WT cells by combining
DDP and metformin, a hypoglycemic drug with low cytotoxicity when
used alone. This microchip system provides a novel tool that has great
potential for the investigation of cell interaction, drug resistance,
and the tumor microenvironment in fundamental and clinical medicine