%0 Journal Article
%T ¦Â1 integrin mediates an alternative survival pathway in breast cancer cells resistant to lapatinib
%A Catherine Huang
%A Catherine C Park
%A Susan G Hilsenbeck
%A Robin Ward
%A Mothaffar F Rimawi
%A Yen-chao Wang
%A Jiang Shou
%A Mina J Bissell
%A C Kent Osborne
%A Rachel Schiff
%J Breast Cancer Research
%D 2011
%I BioMed Central
%R 10.1186/bcr2936
%X We developed a panel of HER2-overexpressing cell lines resistant to L, T, and the potent LT combination through long-term exposure and validated these models in 3D culture. Parental and L/T/LT-resistant cells were subject to HER2 and ¦Â1 integrin inhibitors in 3D and monitored for 12 days, followed by quantification of colony number. Parallel experiments were conducted where cells were either stained for Ki-67 and Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) or harvested for protein and analyzed by immunoblot. Results were subjected to statistical testing using analysis of variance and linear contrasts, followed by adjustment with the Sidak method.Using multiple cell lines including BT474 and HCC1954, we reveal that in L and LT resistance, where phosphorylation of EGFR/HER1, HER2, and HER3 are strongly inhibited, kinases downstream of ¦Â1 integrin--including focal adhesion kinase (FAK) and Src--are up-regulated. Blockade of ¦Â1 by the antibody AIIB2 abrogates this up-regulation and functionally achieves significant growth inhibition of L and LT resistant cells in 3D, without dramatically affecting the parental cells. SiRNA against ¦Â1 as well as pharmacologic inhibition of FAK achieve the same growth inhibitory effect. In contrast, trastuzumab-resistant cells, which retain high levels of phosphorylated EGFR/HER1, HER2, and HER3, are only modestly growth-inhibited by AIIB2.Our data suggest that HER2 activity, which is suppressed in resistance involving L but not T alone, dictates whether ¦Â1 mediates an alternative pathway driving resistance. Our findings justify clinical studies investigating the inhibition of ¦Â1 or its downstream signaling moieties as strategies to overcome acquired L and LT resistance.The HER signaling pathway is one of the most studied and prominent drivers of human breast cancer progression. Aberrant overexpression, activation, and dimerization of the individual members of the HER family--comprised of EGFR (Epidermal Growth Fa
%U http://breast-cancer-research.com/content/13/4/R84