TY - JOUR AB - Our recent observations indicated that RAFTK (also termed Pyk2 and CAK-β) participated in intracellular signaling upon heregulin (HRG) stimulation and promoted breast carcinoma invasion. Furthermore, studies from our group indicate that the Csk homologous kinase (CHK), a member of the Csk family, directly associates with HER2/Neu and down-regulates HER2/Neu-mediated Src kinase activation in breast cancer cells upon heregulin stimulation. Since activation of RAFTK is associated with the activity of Src family kinases, we analyzed whether CHK is capable of opposing HRG-induced activation of RAFTK. Stimulation of human T47D breast cancer cells with HRG induced the tyrosine phosphorylation of RAFTK and its association with CHK in vitro and in vivo. This interaction was mediated through the Src binding site (amino acid residue at 402) of RAFTK and the SH2 domain of CHK. RAFTK phosphorylation downstream of the activated HER2/Neu was greatly reduced in the presence of CHK. Maximal inhibition of RAFTK phosphorylation by CHK required the kinase activity of CHK. Furthermore, CHK inhibited the tyrosine phosphorylation of the focal adhesion-associated protein, paxillin, and inhibited HRG-induced T47D breast cancer cell migration. These findings indicate the role of CHK as a negative regulator in HRG- and RAFTK-mediated intracellular signaling in breast cancer cells. AD - Fox Chase Cancer Center, Department of Medical Oncology, Philadelphia, PA 19111, USA null AU - McShan,Gina,D. AU - Zagozdzon,Radoslaw AU - Park,Shin-Young AU - Zrihan-Licht,Sheila AU - Fu,Yigong AU - Avraham,Shalom AU - Avraham,Hava DA - 2002/07/01 DO - 10.3892/ijo.21.1.197 EP - 205 IS - 1 JO - Int J Oncol PY - 2002 SN - 1019-6439 1791-2423 SP - 197 ST - Csk homologous kinase associates with RAFTK/Pyk2 in breast cancer cells and negatively regulates its activation and breast cancer cell migration T2 - International Journal of Oncology TI - Csk homologous kinase associates with RAFTK/Pyk2 in breast cancer cells and negatively regulates its activation and breast cancer cell migration UR - https://doi.org/10.3892/ijo.21.1.197 VL - 21 ER -