| Literature DB >> 28645565 |
Mariana L Oliveira1, Padma Akkapeddi1, Isabel Alcobia2, Afonso R Almeida1, Bruno A Cardoso1, Rita Fragoso1, Teresa L Serafim1, João T Barata3.
Abstract
T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological cancer that arises from clonal expansion of transformed T-cell precursors. In this review we summarize the current knowledge on the external stimuli and cell-intrinsic lesions that drive aberrant activation of pivotal, pro-tumoral intracellular signaling pathways in T-cell precursors, driving transformation, leukemia expansion, spread or resistance to therapy. In addition to their pathophysiological relevance, receptors and kinases involved in signal transduction are often attractive candidates for targeted drug development. As such, we discuss also the potential of T-ALL signaling players as targets for therapeutic intervention.Entities:
Keywords: Genetics; Interleukin-7 receptor; Microenvironment; Notch; Signaling therapies; T-cell acute lymphoblastic leukemia
Mesh:
Year: 2017 PMID: 28645565 DOI: 10.1016/j.cellsig.2017.06.011
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315