Mechanical Regulation of Redox Balance via the Induction of the PIN1/NRF2/ARE Axis in Pancreatic Cancer

Pancreatic cancer is one of the most lethal malignancies. Desmoplastic stroma and metabolic reprogramming are two hallmarks of pancreatic cancer that support its malignant biological behaviors. However, the underlying mechanism by which the stroma maintain the redox balance remains unclear in pancreatic ductal adenocarcinoma (PDAC). Here, we demonstrated that the physical properties of the stroma could regulate the expression of PIN1 in pancreatic cancer cells. Moreover, we found that hard matrix-cultured pancreatic cancer cells induced the upregulation of PIN1 expression. Since PIN1 maintained redox balance via synergistic activation of NRF2 transcription, PIN1 promoted the expression of NRF2 to induce the expression of intracellular antioxidant response element (ARE)-driven genes. Consequently, the antioxidant stress ability of PDAC was increased, and the intracellular level of reactive oxygen species (ROS) was decreased. Thus, PIN1 is expected to be an important target for the treatment of PDAC, especially PDAC with an exuberant desmoplastic stroma.

Automated summary

Pancreatic cancer is a highly deadly malignancy with desmoplastic stroma and metabolic reprogramming as its key features. The underlying mechanism of the stroma's role in maintaining redox balance in pancreatic ductal adenocarcinoma (PDAC) remains unclear. This study demonstrates that the physical properties of the stroma can regulate the expression of PIN1 in PDAC cells. PIN1, through its synergistic activation of NRF2 transcription, promotes the expression of intracellular antioxidant response element (ARE)-driven genes, leading to increased antioxidant stress ability and decreased intracellular level of reactive oxygen species (ROS) in PDAC.