The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer.
Stefanie TiedeNathalie Meyer-SchallerRavi Kiran Reddy KalathurRobert IvanekErnesta FagianiPhilip SchmassmannPatrick StillhardSimon HäfligerNorbert KrautNorbert SchweiferIrene C WaizeneggerRuben BillGerhard ChristoforiPublished in: Oncogenesis (2018)
Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that regulates a plethora of downstream signaling pathways essential for cell migration, proliferation and death, processes that are exploited by cancer cells during malignant progression. These well-established tumorigenic activities, together with its high expression and activity in different cancer types, highlight FAK as an attractive target for cancer therapy. We have assessed and characterized the therapeutic potential and the biological effects of BI 853520, a novel small chemical inhibitor of FAK, in several preclinical mouse models of breast cancer. Treatment with BI 853520 elicits a significant reduction in primary tumor growth caused by an anti-proliferative activity by BI 853520. In contrast, BI 853520 exerts effects with varying degrees of robustness on the different stages of the metastatic cascade. Together, the data demonstrate that the repression of FAK activity by the specific FAK inhibitor BI 853520 offers a promising anti-proliferative approach for cancer therapy.
Keyphrases
- cell migration
- cancer therapy
- tyrosine kinase
- signaling pathway
- drug delivery
- epidermal growth factor receptor
- squamous cell carcinoma
- small cell lung cancer
- poor prognosis
- stem cells
- magnetic resonance imaging
- epithelial mesenchymal transition
- papillary thyroid
- staphylococcus aureus
- deep learning
- bone marrow
- escherichia coli
- electronic health record
- cystic fibrosis
- young adults
- biofilm formation
- oxidative stress
- protein kinase