Journal of Biochemistry Advance Access published online on March 3, 2008
Journal of Biochemistry, doi:10.1093/jb/mvn032
© 2008 The Japanese Biochemical Society
Erbin regulated sensitivity of MCF-7 breast cancer cells to TRAIL via ErbB2/AKT/NF-
B pathway
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, 5 Dong Dan San Tiao, Beijing 100005, CHINA
*To whom correspondence s 'Erbin regulated sensitivity of MCF-7 to TRAIL via ErbB2 pathway' hould be addressed: Dexian Zheng, Institute of Basic Medical Sciences, 5 Dong Dan San Tiao, Beijing 100005, CHINA, Tel. 8610 6529 6409 Fax: 8610 6510 5102, E-mail: zhengdx{at}pumc.edu.cn or zhengdx{at}tom.com
Received December 28, 2007; Accepted February 19, 2008
| Abstract |
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We have reported that Erbin expression was down-regulated in the Jurkat leukemia T lymphocytes treated with the recombinant soluble tumor necrosis factor-related apoptosis-inducing ligand (rsTRAIL). Herein, we studied the expression and the regulation of Erbin and its binding partner, ErbB2, in the MCF-7 breast cancer cell line. We showed that the expressions of Erbin and ErbB2 were modulated by PKC
inhibitor, rottlerin, in the TRAIL-resistant MCF-7 cell line. The affinity of Erbin-ErbB2 interaction was reduced by ErbB2 phosphorylation. Inhibiting the expression of Erbin facilitated the sensitivity of the MCF-7 cells to TRAIL via suppressing the ErbB2/AKT/NF-
B signaling pathway.
Key Words: Erbin, rsTRAIL, ErbB2, apoptosis, breast cancer