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The TAM receptor family of TYRO3, AXL and MERTK regulates tissue and immune homeostasis. Aberrant TAM receptor signalling has been linked to a range of diseases, including cancer, fibrosis and viral infections. Specifically, the dysregulation of TAM receptors can enhance tumour growth and metastasis due to their involvement in multiple oncogenic pathways. For example, TAM receptors have been implicated in the epithelial-mesenchymal transition, maintaining the stem cell phenotype, immune modulation, proliferation, angiogenesis and resistance to conventional and targeted therapies. Therapeutically, multiple TAM receptor inhibitors are in preclinical and clinical development for cancers and other indications, with those targeting AXL being the most clinically advanced. Although there has been notable clinical advancement in recent years, challenges persist. This Review aims to provide both biological and clinical insights into the current therapeutic landscape of TAM receptor inhibitors, and evaluates their potential for the treatment of cancer and non-malignant diseases.

Original publication

DOI

10.1038/s41573-023-00846-8

Type

Journal

Nat Rev Drug Discov

Publication Date

03/2024

Volume

23

Pages

201 - 217

Keywords

Humans, Receptor Protein-Tyrosine Kinases, Axl Receptor Tyrosine Kinase, Proto-Oncogene Proteins, c-Mer Tyrosine Kinase, Neoplasms