A functional nuclear epidermal growth factor receptor, SRC and Stat3 heteromeric complex in pancreatic cancer cells.

Evidence is presented for the nuclear presence of a functional heteromeric complex of epidermal growth factor (EGFR), Src and the Signal Transducer and Activator of Transcription (Stat)3 proteins in pancreatic cancer cells. Stat3 remains nuclear and associated with Src or EGFR, respectively, upon the siRNA knockdown of EGFR or Src, ...
demonstrating the resistance of the complex to the modulation of EGFR or Src alone. Significantly, chromatin immunoprecipitation (ChIP) analyses reveal the nuclear EGFR, Src and Stat3 complex is bound to the c-Myc promoter. The siRNA knockdown of EGFR or Src, or the pharmacological inhibition of Stat3 activity only marginally suppressed c-Myc expression. By contrast, the concurrent modulation of Stat3 and EGFR, or Stat3 and Src, or EGFR and Src strongly suppressed c-Myc expression, demonstrating that the novel nuclear heteromeric complex intricately regulates the c-Myc gene. The prevalence of the transcriptionally functional EGFR, Src, and Stat3 nuclear complex provides an additional and novel mechanism for supporting the pancreatic cancer phenotype and explains in part the insensitivity of pancreatic cancer cells to the inhibition of EGFR, Src or Stat3 alone.
Mesh Terms:
Cell Line, Tumor, Cell Nucleus, Chromatin Immunoprecipitation, Endocytosis, Fluorescent Antibody Technique, Gene Expression Regulation, Neoplastic, Humans, Immunoblotting, Immunoprecipitation, Light, Microscopy, Confocal, Multiprotein Complexes, Nanoparticles, Nanotechnology, Pancreatic Neoplasms, Particle Size, Protein Binding, Proto-Oncogene Proteins c-myc, Proto-Oncogene Proteins pp60(c-src), Receptor, Epidermal Growth Factor, STAT3 Transcription Factor, Scattering, Radiation
PLoS ONE
Date: May. 17, 2011
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