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. 2020 Apr 19;39(25):4781–4797. doi: 10.1038/s41388-020-1284-6

Fig. 4. Increased ERBB signalling following sustained palbociclib resistance.

Fig. 4

a Antiproliferative effect of neratinib in MCF7, MCF7 LTED, T47D, T47D LTED and HCC1428 LTED and their corresponding palbociclib-resistant (PalboR) derivatives. Data represents % viable cells compared with vehicle control for each cell line. Error bars represent mean ± SEM. b Effect of escalating concentrations of fulvestrant both in the presence or absence of neratinib (500 nM) in MCF7, MCF7 LTED, T47D, T47D LTED and HCC1428 LTED and their corresponding palbociclib-resistant (PalboR) cell lines. Data represents % viable cells. Error bars represent mean ± SEM. c Schematic representation of the effect of CDK4/6 inhibition and cross-talk with receptor tyrosine kinase signalling pathway. d Immunoblotting showing expression levels of several cell cycle, growth factor signalling and ER-regulated markers in MCF7 LTEDPalboR cell lines following single treatment with palbociclib (1 μM) or in combination with neratinib (500 nM) over a time course of 24 h. e Immunobloting showing abundance of nuclear ER in MCF7 LTEDPalboR cell lines after treatment with palbociclib (1 μM), neratinib (500 nM) or the combination of both.