Table 1.
Axl in resistance in cancer treatment.
Cancer Type | Drug (s) | Drug Target (s) | Model (Human, Animal, Cell Line) | Refs. |
---|---|---|---|---|
NSCLC | Erlotinib, Gefitinib | EGFR | Human | [57] |
Cetuximab | EGFR | Cell line | [19] | |
Osimertinib | EGFR | Cell line | [58] | |
Crizotinib | ALK, c-Met | Cell line | [59] | |
Cisplatin | Interferes with DNA damage repair mechanism | Cell line | [60] | |
Doxorubicin | Inhibition of DNA topoisomerase II activity | Cell line | [60] | |
Etoposide | Inhibition of DNA topoisomerase II activity | Cell line | [60] | |
Paclitaxel | Microtubule polymer stabilizer | Cell line | [61] | |
Vincristine | Binds to tubulin and inhibits the formation of microtubules | Cell line | [61] | |
EGFR-mutant NSCLC | Erlotinib | EGFR | Mouse, cell line | [62] |
Prostate | Docetaxel | Inhibitor of depolymerisation of microtubules | Cell line | [63] |
Breast | Lapatinib | EGFR, HER2 | Cell line | [64] |
Erlotinib | EGFR | Cell line | [31] | |
AZD8931 (Sapitinib) | EGFR, HER2, HER3 | Cell line | [65] | |
Fluorouracil | Inhibits DNA/RNA replication | Cell line | [66] | |
Paclitaxel | Tubulin Inhibitor (Microtubule polymer stabilizer) | Cell line | [67] | |
Liver | Erlotinib, Gefitinib | EGFR | Cell line | [68] |
Sorafenib | Raf-1, B-Raf, VEGFR, PDGFR, Flt-3 and c-KIT | Cell line | [69] | |
Head and neck squamous cell carcinoma | Cetuximab | EGFR | PDX | [19] |
Erlotinib, Gefitinib | EGFR | Cell line | [70] | |
BYL719 | PI3Kα | Cell line | [71] | |
Cisplatin, Carboplatin | Interferes with DNA damage repair mechanism | Cell line | [72] | |
ESCC | Lapatinib | EGFR, HER2 | Cell line | [73] |
Gastrointestinal stromal tumour | Imatinib mesylate | v-Abl, c-KIT, PDGFR | Cell line | [74] |
Neuroblastoma | TAE684, LDK378 | ALK | Cell line | [75] |
Rhabdomyosarcoma | MAB391 | IGF-IR | Cell line | [76] |
Acute myeloid leukaemia | PKC412 | PKCα/β/γ, Syk, Flk-1, AKT, PKA, c-Kit, c-Fgr, c-Src, FLT3, PDFRβ, and VEGFR1/2 | Cell line | [77] |
AC220 | FLT3 | Cell line | [77] | |
Doxorubicin plus cytosine arabinoside | Inhibition of DNA topoisomerase II activity and synthesis of DNA | Human, Cell line | [53] | |
Cisplatin | Interferes with DNA damage repair mechanism | Cell line | [53] |
Abbreviations: ALK, Anaplastic lymphoma kinase; c-Met, hepatocyte growth factor receptor; EGFR, epidermal growth factor receptor; ESCC, oesophageal squamous-cell carcinomas; FLT3, fms-like tyrosine kinase 3; HER2, human epidermal growth factor receptor 2; HER3, human epidermal growth factor receptor 3; IGF-1R, insulin-like growth factor 1 receptor; NSCLC, non-small cell lung cancer; PDGFR, platelet-derived growth factor receptor; PDX, patient-derived xenograft models; PI3Kα, phosphoinositide 3-kinase alpha; VEGFR, vascular endothelial growth factor receptor.