CIP2A overexpression induces autoimmune response and enhances JNK signaling pathway in human lung cancer

BMC Cancer. 2015 Nov 11:15:895. doi: 10.1186/s12885-015-1899-0.

Abstract

Background: Cancerous inhibitor of PP2A (CIP2A) is a recently characterized oncoprotein, which promotes cancer cell proliferation. But the role of CIP2A in lung cancer progression is still not well understood.

Methods: The expression level of CIP2A in lung cancer tissues was examined by immunohistochemistry. CIP2A-associated cell proliferation was performed by knock down or overexpression of CIP2A in lung cancer cells. Phospho-array was used to screen kinase candidates related to expression change of CIP2A. Western-blot and luciferase reporter assay were used to validate phospho-array results.

Results: Overexpression of CIP2A in lung cancer not only triggers immune response in lung cancer patients but also promotes lung cancer cell proliferation. By phospho-array, several kinase candidates were identified, one of which is c-Jun activated kinases (JNK). The knock down of CIP2A decreased JNK phosphorylation, and the phosphorylation of downstream transcriptional factors, ATF2 and c-Jun, whose transcriptional activity were decreased as well. Furthermore, the expression level of CIP2A also affected the phosphorylation of the upstream kinase of JNK, MKK4/MKK7. At last, treatment with JNK inhibitor partially abolished CIP2A-induced cell proliferation.

Conclusion: CIP2A is a tumor-associated autoantigen in lung cancer, which promote lung cancer proliferation partially through MKK4/7-JNK signaling pathway.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Autoantibodies / blood
  • Autoantibodies / immunology
  • Autoantigens / genetics*
  • Autoantigens / immunology
  • Autoantigens / metabolism
  • Autoimmunity / genetics*
  • Case-Control Studies
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Expression*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Lung Neoplasms / etiology*
  • Lung Neoplasms / metabolism*
  • MAP Kinase Kinase 4 / metabolism
  • MAP Kinase Kinase 7 / metabolism
  • Membrane Proteins / genetics*
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism
  • Proto-Oncogene Proteins c-jun / metabolism
  • Signal Transduction*

Substances

  • Autoantibodies
  • Autoantigens
  • CIP2A protein, human
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Proto-Oncogene Proteins c-jun
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • MAP Kinase Kinase 7