Adipocytes enhance murine pancreatic cancer growth via a hepatocyte growth factor (HGF)-mediated mechanism. (April 2016)

• Record Type: Journal Article
• Authors: Ziegler, Kathryn M.; Considine, Robert V.; True, Eben; Swartz-Basile, Deborah A.; Pitt, Henry A.; Zyromski, Nicholas J.
• Is Part Of: International journal of surgery. Volume 28(2016)
• Page Start: 179
• Page End: 184
• Publication Date: 2016-04
• Subjects: Adipocytes -- Pancreatic cancer -- Hepatocyte growth factor -- Obesity; Surgery -- Periodicals; Surgical Procedures, Operative -- Periodicals; 617.005
• DOI: 10.1016/j.ijsu.2016.03.002
• Languages: English
• ISSNs: 1743-9191

Abstract

Abstract: Introduction: Obesity accelerates the development and progression of pancreatic cancer, though the mechanisms underlying this association are unclear. Adipocytes are biologically active, producing factors such as hepatocyte growth factor (HGF) that may influence tumor progression. We therefore sought to test the hypothesis that adipocyte-secreted factors including HGF accelerate pancreatic cancer cell proliferation. Material and methods: Murine pancreatic cancer cells (Pan02 and TGP-47) were grown in a) conditioned medium (CM) from murine F442A preadipocytes, b) HGF-knockdown preadipocyte CM, c) recombinant murine HGF at increasing doses, and d) CM plus HGF-receptor (c-met) inhibitor. Cell proliferation was measured using the MTT assay. ANOVA and t -test were applied; p < 0.05 considered significant. Results: Wild-type preadipocyte CM accelerated Pan02 and TGP-47 cell proliferation relative to control (59 ± 12% and 34 ± 12%, p < 0.01, respectively). Knockdown of preadipocyte HGF resulted in attenuated proliferation vs. wild type CM in Pan02 cells (35 ± 5% vs. 68 ± 14% greater than control; p < 0.05), but proliferation in TGP-47 cells remained unchanged. Recombinant HGF dose-dependently increased Pan02, but not TGP-47, proliferation (p < 0.05). Inhibition of HGF receptor, c-met, resulted in attenuated proliferation versus control in Pan02 cells, but not TGP-47 cells. Conclusions: These experiments demonstrate that adipocyte-derived factors accelerate murine pancreatic cancer proliferation. In the case of Pan02 cells, HGF is responsible, in part, for this proliferation. Highlights: Adipocyte conditioned media accelerated pancreatic cancer cell proliferation. Knockdown of adipocyte hepatocyte growth factor (HGF) attenuated pancreatic cell proliferation. Recombinant HGF dose-dependently increased proliferation of Pan02 pancreatic cancer cells. Inhibition of HGF receptor (c-met) attenuated proliferation of Pan02 pancreatic cancer cells.