Src Family Kinases as Therapeutic Targets in Advanced Solid Tumors: What We Have Learned so Far.
Stefano MartellucciLetizia ClementiSamantha SabettaVincenzo MatteiLorenzo BottaAdriano AngelucciPublished in: Cancers (2020)
Src is the prototypal member of Src Family tyrosine Kinases (SFKs), a large non-receptor kinase class that controls multiple signaling pathways in animal cells. SFKs activation is necessary for the mitogenic signal from many growth factors, but also for the acquisition of migratory and invasive phenotype. Indeed, oncogenic activation of SFKs has been demonstrated to play an important role in solid cancers; promoting tumor growth and formation of distant metastases. Several drugs targeting SFKs have been developed and tested in preclinical models and many of them have successfully reached clinical use in hematologic cancers. Although in solid tumors SFKs inhibitors have consistently confirmed their ability in blocking cancer cell progression in several experimental models; their utilization in clinical trials has unveiled unexpected complications against an effective utilization in patients. In this review, we summarize basic molecular mechanisms involving SFKs in cancer spreading and metastasization; and discuss preclinical and clinical data highlighting the main challenges for their future application as therapeutic targets in solid cancer progression.
Keyphrases
- tyrosine kinase
- papillary thyroid
- clinical trial
- induced apoptosis
- end stage renal disease
- squamous cell
- signaling pathway
- ejection fraction
- newly diagnosed
- childhood cancer
- chronic kidney disease
- lymph node
- prognostic factors
- cell therapy
- lymph node metastasis
- risk factors
- cell cycle arrest
- stem cells
- electronic health record
- big data
- transcription factor
- endoplasmic reticulum stress
- mesenchymal stem cells
- binding protein
- artificial intelligence
- deep learning
- bone marrow
- drug delivery