Kinase Inhibitors' Effects on Innate Immunity in Solid Cancers.
Chunying PengKatrin RaboldWillem J M MulderMartin JaegerRomana T Netea-MaierPublished in: Cancers (2021)
Innate immune cells constitute a plastic and heterogeneous cell population of the tumor microenvironment. Because of their high tumor infiltration and close interaction with resident tumor cells, they are compelling targets for anti-cancer therapy through either ablation or functionally reprogramming. Kinase inhibitors (KIs) that target aberrant signaling pathways in tumor proliferation and angiogenesis have been shown to have additional immunological effects on myeloid cells that may contribute to a protective antitumor immune response. However, in patients with malignancies, these effects are poorly described, warranting meticulous research to identify KIs' optimal immunomodulatory effect to support developing targeted and more effective immunotherapy. As many of these KIs are currently in clinical trials awaiting approval for the treatment of several types of solid cancer, we evaluate here the information on this drug class's immunological effects and how such mechanisms can be harnessed to improve combined treatment regimens in cancer.
Keyphrases
- induced apoptosis
- cancer therapy
- clinical trial
- signaling pathway
- immune response
- papillary thyroid
- cell cycle arrest
- innate immune
- drug delivery
- dendritic cells
- squamous cell
- bone marrow
- randomized controlled trial
- emergency department
- healthcare
- pi k akt
- endoplasmic reticulum stress
- acute myeloid leukemia
- cell therapy
- toll like receptor
- stem cells
- endothelial cells
- cell death
- cell proliferation
- single cell
- electronic health record
- phase iii