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EGFR negates the proliferative effect of oncogenic HER2 in MDA-MB-231 cells
- Oh, Sunhwa, Ju, Ji-hyun, Yang, Wonseok, Lee, Kyung-min, Nam, KeeSoo, Shin, Incheol
- Archives of biochemistry and biophysics 2015 v.575 pp. 69-76
- breasts, cell growth, cell lines, dimerization, growth and development, ligands, proteins, tyrosine
- Members of the EGFR family are potent mediators of normal cell growth and development. HER2 possesses an active tyrosine kinase domain, but no direct ligand has been identified. To investigate the differential effect of HER2 in breast cell lines, HER2 was overexpressed in MCF-10A, MCF7 and MDA-MB-231 cells. HER2 overexpression promoted proliferation, survival and migration in MCF-10A and MCF-7 cells. No significant differences were seen in proliferation, survival or migration between MDA-MB-231 vec and HER2 cells. The activity of downstream HER2 proteins increased in MCF-10A HER2 and MCF-7 HER2 cells but not in MDA-MB-231 HER2 cells. Exogenously expressed HER2 failed to associate with EGFR or HER3 in MDA-MB-231 cells, while overexpression of HER2 enhanced HER family dimerization in MCF-10A and MCF-7 cells.