Tinagl1 Suppresses Triple-Negative Breast Cancer Progression and Metastasis by Simultaneously Inhibiting Integrin/FAK and EGFR Signaling

作者：Shen, Minhong; Jiang, Yi-Zhou; Wei, Yong; Ell, Brian; Sheng, Xinlei; Esposito, Mark; Kang, Jooeun; Hang, Xiang; Zheng, Hanqiu; Rowicki, Michelle; Zhang, Lanjing; Shih, Weichung J.; Celia-Terrassa, Toni; Liu, Yirong; Cristea, Ileana; Shao, Zhi-Ming; Kang, Yibin^*

来源：Cancer Cell, 2019, 35(1): 64-+.

DOI：10.1016/j.ccell.2018.11.016

• EPIDERMAL-GROWTH-FACTOR
• GENE-EXPRESSION
• FACTOR RECEPTOR
• CELLS
• ADHESION
• FAK
• RESISTANCE
• COMBINATION
• DISRUPTION
• ACTIVATION

Triple-negative breast cancer (TNBC) patients have the worst prognosis and distant metastasis-free survival among all major subtypes of breast cancer. The poor clinical outlook is further exacerbated by a lack of effective targeted therapies for TNBC. Here we show that ectopic expression and therapeutic delivery of the secreted protein Tubulointerstitial nephritis antigen-like 1 (Tinagl1) suppresses TNBC progression and metastasis through direct binding to integrin alpha 5 beta 1, alpha v beta 1, and epidermal growth factor receptor (EGFR), and subsequent simultaneous inhibition of focal adhesion kinase (FAK) and EGFR signaling pathways. Moreover, Tinagl1 protein level is associated with good prognosis and reversely correlates with FAK and EGFR activation status in TNBC. Our results suggest Tinagl1 as a candidate therapeutic agent for TNBC by dual inhibition of integrin/FAK and EGFR signaling pathways.

• 出版日期2019-1-14
• 单位复旦大学; 中国医科大学; rutgers