The Inflammatory Calcium Binding Protein S100A8 and Its N-Terminal Proteolytic Fragment Interact with Transforming Growth Factor-Beta1 (TGF-b1) and Alter Akt, mTOR and NF-kappa B Cancer Cell Signalling

  • Dania Bozzato Department of Medicine, University of Padua. Padua, Italy
  • Stefania Moz Department of Medicine, University of Padua. Padua, Italy
  • Andrea Padoan Department of Medicine, University of Padua. Padua, Italy
  • Michele Scorzeto Department of Biomedical Sciences, University of Padua. Padua, Italy
  • Paola Fogar Department of Medicine, University of Padua. Padua, Italy
  • Cosimo Sperti Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua. Padua, Italy
  • Eliana Greco Department of Medicine, University of Padua. Padua, Italy
  • Carlo Federico Zambon Department of Medicine, University of Padua. Padua, Italy
  • Filippo Navaglia Department of Medicine, University of Padua. Padua, Italy
  • Michele Pelloso Department of Medicine, University of Padua. Padua, Italy
  • Elisa Rossi Department of Medicine, University of Padua. Padua, Italy
  • Claudio Pasquali Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua. Padua, Italy
  • Sergio Pedrazzoli Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua. Padua, Italy
  • Carlo Reggiani Department of Biomedical Sciences, University of Padua. Padua, Italy
  • Mario Plebani Department of Medicine, University of Padua. Padua, Italy
  • Daniela Basso Department of Medicine, University of Padua. Padua, Italy
Keywords: Meeting Abstracts, Pancreas

Abstract

Context S100A8 is highly expressed by stromal cells in pancreatic cancer when SMAD4 is not mutated or by cancer cells when SMAD4 is mutated, suggesting a link between TGF-β1 and S100A8 pathways. The proteolytic fragment of S100A8, NT-S100A8, highly abundant in pancreatic cancer, is involved in altering insulin secretion and action. Objective To ascertain whether S100A8 and NT-S100A8 interacts with TGF-β1 in altering intracellular calcium, NF-kappa B, Akt and mTOR signalling. Methods BxPC3 cells were stimulated with S100A8 (10 nM), NT-S100A8 (50 nM) alone or combined with TGF-β1 (0.02 ng/mL). Intracellular calcium was monitored by Fluo4 (epifluroescence). Akt (Ser473,Thr308), mTOR (Ser2448), NF-kappa B (p-IkB-a) were WB analyzed. Results NT-S100A8 evoked a train of intracellular calcium fluxes after 150-second lag time, which was reduced to few seconds in the presence of TGF-β1. S100A8 or TGF-β1 alone did not alter intracellular calcium. NF-kappa B signalling was activated in a calcium-dependent manner by S100A8 and by NT-S100A8 in the presence of TGF-β1. Akt Ser473 phosphorylation was reduced by NT-S100A8, TGF-β1 but mainly by their combination. AktThr308 was not affected by the studied molecules. mTOR phosphorylation (Ser2448) was induced by S100A8 and, at a lesser degree, by TGF-β1 and NT-S100A8. The phosphorylation (Ser235/236) of the downstream effector of mTORC1, S6RB, was reduced by TGF-β1 and NT-S100A8 independently, not by S100A8. Conclusion NT-S100A8 mimics TGF-β1 inhibitory effects on Akt and mTOR signalling. These two molecules co-operate in inhibiting Akt probably by altering intracellular calcium, while they co-operate in activating NF-kappa B in a calcium-independent manner mimicking the entire S100A8 molecule effect.

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Published
2012-09-20
How to Cite
BozzatoD., MozS., PadoanA., ScorzetoM., FogarP., SpertiC., GrecoE., ZambonC., NavagliaF., PellosoM., RossiE., PasqualiC., PedrazzoliS., ReggianiC., PlebaniM., & BassoD. (2012). The Inflammatory Calcium Binding Protein S100A8 and Its N-Terminal Proteolytic Fragment Interact with Transforming Growth Factor-Beta1 (TGF-b1) and Alter Akt, mTOR and NF-kappa B Cancer Cell Signalling. JOP. Journal of the Pancreas, 13(5S), 554. https://doi.org/10.6092/1590-8577/1000

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