A novel FAK-degrading PROTAC molecule exhibited both anti-tumor activities and efficient MDR reversal effects

• Published in: Acta pharmacologica Sinica 2024-10, Vol.45 (10), p.2174-2185
• Main Authors: Xu, Ming-shi, Gu, Xiao-fan, Li, Cong, Pan, Li-xuan, Zhu, Zi-xia, Fan, Meng, Zhao, Yun, Chen, Jian-fang, Liu, Xuan, Zhang, Xiong-wen
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Biomedical and Life Sciences; Biomedicine; Cell Line, Tumor; Cell Proliferation - drug effects; Drug Resistance, Multiple - drug effects; Drug Resistance, Neoplasm - drug effects; Focal Adhesion Kinase 1 - antagonists & inhibitors; Focal Adhesion Kinase 1 - metabolism; Humans; Immunology; Internal Medicine; Medical Microbiology; Mice; Pharmacology/Toxicology; Protein Kinase Inhibitors - chemistry; Protein Kinase Inhibitors - pharmacology; Vaccine
• ISSN: 1671-4083; 1745-7254; 1745-7254
• DOI: 10.1038/s41401-024-01312-w

FAK (focal adhesion kinase) is widely involved in cancer growth and drug resistance development. Thus, FAK inhibition has emerged as an effective strategy for tumor treatment both as a monotherapy or in combination with other treatments. But the current FAK inhibitors mainly concentrate on its kinase activity, overlooking the potential significance of FAK scaffold proteins. In this study we employed the PROTAC technology, and designed a novel PROTAC molecule F2 targeting FAK based on the FAK inhibitor IN10018. F2 exhibited potent inhibitory activities against 4T1, MDA-MB-231, MDA-MB-468 and MDA-MB-435 cells with IC 50 values of 0.73, 1.09, 5.84 and 3.05 μM, respectively. On the other hand, F2 also remarkably reversed the multidrug resistance (MDR) in HCT8/T, A549/T and MCF-7/ADR cells. Both the effects of F2 were stronger than the FAK inhibitor IN10018. To our knowledge, F2 was the first reported FAK-targeted PROTAC molecule exhibiting reversing effects on chemotherapeutic drug resistance, and its highest reversal fold could reach 158 times. The anti-tumor and MDR-reversing effects of F2 might be based on its inhibition on AKT (protein kinase B, PKB) and ERK (extracellular signal-regulated kinase) signaling pathways, as well as its impact on EMT (epithelial-mesenchymal transition). Furthermore, we found that F2 could reduce the protein level of P-gp in HCT8/T cells, thereby contributing to reverse drug resistance from another perspective. Our results will boost confidence in future research focusing on targeting FAK and encourage further investigation of PROTAC with potent in vivo effects.