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PTH-115 Inhibition of mapk signalling promotes cell cycle arrest and sensitises intrahepatic cholangiocarcinoma cells to chemotherapy
  1. PM Choy1,
  2. J Sufi1,2,
  3. S Glaser3,
  4. G Alpini3,
  5. N Heaton4,
  6. R Williams1,5,
  7. A Quaglia4,
  8. W-K Syn5,
  9. C Bubici6,
  10. S Papa1
  1. 1Cell Signalling and Cancer Laboratory, Institute of Hepatology London
  2. 2BSc Program in Gastroenterology and Hepatology, Imperial College London, London, UK
  3. 3Department of Internal Medicine, Scott and White Healthcare and Texas A&M Health Science Center, Temple, Tx, United States
  4. 4Institute of Liver Studies, King’s College Hospital
  5. 5Repair and Regeneration Laboratory, Institute of Hepatology London
  6. 6Division of Biosciences, Brunel University London, London, UK

Abstract

Introduction Intrahepatic cholangiocarcinoma (ICC) is the second most common primary hepatic malignancy, accounting for approximately 15% of cases of primary liver cancer. Although new treatments have increased survival for many other cancers, including the more common primary hepatocellular carcinoma, treatment strategies and survival for patients with ICC have seen little improvement. Our previous studies suggest that the mitogen-activated protein kinase (MAPK) signalling plays a central role in the regulation of cell proliferation in human ICC. However the molecular mechanisms are poorly understood. In this study, we aim to explore whether inhibition of the MAPK pathway and its downstream effectors enhances the sensitisation of ICC cells to the chemotherapeutic agent cisplatinum.

Method We used a combinatorial approach of immunohistochemical and gene expression analyses to investigate the expression of MAPK-related genes in ICC tumours. Furthermore, by using in-vitroand in-vivoanalyses we have characterised the function of a novel MAPK downstream effector in ICC cells.

Results The expression of MAPK signalling was determined by immunohistochemical staining in tumour samples from a cohort of 14 ICC patients. High expression of phospho-activated MAPK was observed in 71.4% (10/14) of ICC cases as compared with surrounding nontumour tissue. Likewise, expression of JDP, a downstream effector of the MAPK signalling, was scored as high intensity in 64.3% (9/14). Strikingly, elevated expression of JDP transcripts was also observed in two independent cohorts of human ICC (n = 149 and n = 109 per group, respectively) compared to surrounding normal liver tissue. Consistent with the in-vivo analyses of human samples, immunoblotting analyses showed constitutive activation of MAPK and expression of JDP in ICC-derived cells (i.e. SG231, CCLP-1 and HuCCT1). Using loss-of-function analyses, we demonstrates that knockdown of JDP in ICC-derived cells resulted in cell cycle arrest and reduced expression of cell cycle regulators (i.e. cyclins), and had minimal effect on apoptosis. Chemical inhibition of JDP significantly sensitises ICC-derived cells to cisplatinum (P < 0.001).

Conclusion These results demonstrate that enhanced activation of MAPK signalling is important for ICC cell proliferation and suggest that targeting its downstream effectors is a potential therapeutic strategy for ICC.

Disclosure of interest None Declared.

Reference

  1. This abstract is funded by Alan Morement Memorial Fund

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