Ny forskningsartikkel fra 16/6 som tar for seg AXL hemming.
There is ample evidence supporting the important role of AXL in drug resistance across various types of cancers. Therefore, targeting AXL is a promising strategy for addressing drug resistance. Drugs that inhibit AXL can be grouped based on their mechanisms of action, including small molecule selective inhibitors (such as BGB324 and TP-0903), antibody–drug conjugates (such as BA3011), anti-AXL Fc fusion protein AVB-S6-500, and multitargeted inhibitors (such as ONO-7475, Merestinib and Sitravatinib) [105]. Experimental data from both in vivo and in vitro studies suggest that carboplatin/paclitaxel combined with AVB-S6-500 is more effective than chemotherapy alone [59]. Additionally, the combination of nivolumab and BGB324 prolongs the survival period of mice with GBM [23]