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.
| Original language | English |
|---|---|
| Pages (from-to) | 10-25 |
| Number of pages | 16 |
| Journal | Cellular Signalling |
| Volume | 38 |
| DOIs | |
| Publication status | Published - Oct 2017 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Genetics
- Interleukin-7 receptor
- Microenvironment
- Notch
- Signaling therapies
- T-cell acute lymphoblastic leukemia
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