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Macrophage colony-stimulating factor 1 (CSF1), also known as M-CSF, is a hematopoietic growth factor and cytokine essential for the survival, proliferation, and differentiation of the monocyte-macrophage lineage (UniProt P09603). It functions by binding to the CSF1 receptor (CSF1R), a tyrosine kinase receptor, triggering downstream signaling pathways like MAPK and PI3K/Akt that regulate cellular processes (NCBI Gene ID: 1435). In many solid tumors, CSF1 is overexpressed by cancer cells, which recruits tumor-associated macrophages (TAMs) that facilitate tumor progression, immunosuppression, and metastasis (PubMed: 26910395). Because of this role, CSF1 is a key target for immunotherapy, with drugs like MCS110 designed to neutralize the ligand and deplete immunosuppressive TAMs within the tumor microenvironment (ClinicalTrials.gov: NCT01643850). Additionally, CSF1 is involved in the pathogenesis of inflammatory diseases such as rheumatoid arthritis and bone disorders like osteoporosis due to its critical role in osteoclast development and maturation (PubMed: 22438718). Therapeutic intervention typically involves monoclonal antibodies to block the ligand-receptor axis, though safety monitoring for liver toxicity and bone health is required.
Ligand neutralization via monoclonal antibodies to prevent binding and activation of the CSF1 receptor (CSF1R), or administration of recombinant ligand as an agonist.
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