ErbB4/KITENIN-Mediated Signaling is Activated in Cetuximab-Resistant Colorectal Cancer Cells

被引:6
作者
Park, So-Yeon [1 ]
Yang, Yi [1 ]
Zhou, Rui [1 ]
Jung, Sang-Chul [2 ]
Bae, Woo Kyun [3 ]
Chung, Lk Joo [3 ]
Kim, Kyung Keun [4 ]
Kim, Hangun [1 ]
机构
[1] Sunchon Natl Univ, Coll Pharm, Sunchon 57922, Jeonnam, South Korea
[2] Sunchon Natl Univ, Dept Environm Engn, Sunchon 57922, Jeonnam, South Korea
[3] Chonnam Natl Univ, Med Sch, Dept Hematol Oncol, Gwangju 61469, South Korea
[4] Chonnam Natl Univ, Med Sch, Med Res Ctr Gene Regulat, Gwangju 61469, South Korea
基金
新加坡国家研究基金会;
关键词
ErbB4; KITENIN; EGFR; Cetuximab; Resistance; Colorectal Cancer; EGFR-TARGETED THERAPIES; LUNG-CANCER; KITENIN; ERBB4;
D O I
10.1166/jnn.2019.15899
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
ErbB4/KITENIN signaling plays a role in epidermal growth factor receptor (EGFR)-independent EGF pathways mediating the invasiveness and tumorigenesis of colorectal cancer cells. However, whether alterations in ErbB4/KITENIN signaling play a role in the resistance to anti-EGFR therapy remains unclear. Here, we established cetuximab-resistant DLD1 and HT29 cells, and analyzed changes in ErbB4/KITENIN signaling. c-Jun, a final effector in ErbB4/KITENIN-mediated signaling, was upregulated, whereas KITENIN levels remained constant in both cetuximab-resistant cell lines. The phosphorylation of EGFR and ErbB4 was increased in cetuximab-resistant cells, suggesting that ErbB4/KITENIN signaling contributed to the acquisition of cetuximab resistance in the cells. Silencing of KITENIN and/or ErbB4 increased cetuximab sensitivity in cetuximab-resistant cells. This study is the first to report the activation of ErbB4/KITENIN-mediated signaling in cetuximab-resistant colorectal cancer cells and the potential clinical application of ErbB4/KITENIN-targeting therapy for overcoming anti-EGFR resistance.
引用
收藏
页码:1166 / 1171
页数:6
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