AI Article Synopsis

  • Caveolin 1 (Cav-1) is a protein that influences various signaling pathways, interacting significantly with LRP6 to regulate Wnt-β-catenin signaling, which is crucial in prostate cancer.
  • There’s a positive correlation between Cav-1 and LRP6 expression in prostate cancer tissues, and their interactions also elevate levels of c-Myc and promote aerobic glycolysis through Akt signaling.
  • Cav-1 and LRP6 work together to enhance IGF-IR/IR signaling, leading to increased Akt-mTORC1 activity, which supports cancer metabolism and progression.

Article Abstract

Caveolin 1 (Cav-1) is a plasma membrane-associated protein with the capacity to modulate signaling activities in a context-dependent fashion. Interactions between Cav-1 and low-density lipoprotein receptor-related protein 6 (LRP6) were reported to be important for the regulation of Wnt-β-catenin (β-cat) signaling. Cav-1 also interacts with insulin and IGF-I receptors (IGF-IR/IR) and can stimulate IR kinase activities. We found positive correlation between Cav-1 and LRP6 expression in both human primary prostate cancer and metastasis tissues and in PC-3 cells. Cav-1 stimulation of Wnt-β-cat signaling and c-Myc levels was positively associated with LRP6 expression in LNCaP, PC-3, and DU145 prostate cancer cells. Importantly, LRP6 and, to a lesser extent, Cav-1 were found to stimulate aerobic glycolysis. These activities were positively associated with the expression of HK2 and Glut3 and shown to be dependent on Akt signaling by both gene knockdown and chemical inhibition methods. We further showed that Cav-1 and LRP6 exert their effects on Akt and glycolytic activities by stimulating IGF-IR/IR signaling. Overall, our results show that Cav-1 interacts with LRP6 to generate an integrated signaling module that leads to the activation of IGF-IR/IR and results in stimulation of Akt-mTORC1 signaling and aerobic glycolysis in prostate cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688259PMC
http://dx.doi.org/10.1158/0008-5472.CAN-12-3040DOI Listing

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