Abstract
Tumor progression requires cancer cell proliferation, migration, invasion, and attraction of blood and lymph vessels. These processes are tightly regulated by growth factors and their intracellular signaling pathways, which culminate in transcriptional programs. Hence, oncogenic mutations often capture growth factor signaling, and drugs able to intercept the underlying biochemical routes might retard cancer spread. Along with messenger RNAs, microRNAs play regulatory roles in growth factor signaling and in tumor progression. Because growth factors regulate abundance of certain microRNAs and the latter modulate the abundance of proteins necessary for growth factor signaling, the two classes of molecules form a dense web of interactions, which are dominated by a few recurring modules. We review specific examples of the alliance formed by growth factors and microRNAs and refer primarily to the epidermal growth factor (EGF) pathway. Clinical applications of the crosstalk between microRNAs and growth factors are described, including relevance to cancer therapy and to emergence of resistance to specific drugs.
| Original language | English |
|---|---|
| Pages (from-to) | 1578-1599 |
| Number of pages | 22 |
| Journal | Journal of Clinical Medicine |
| Volume | 4 |
| Issue number | 8 |
| DOIs | |
| State | Published - 13 Aug 2015 |
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
- Cancer therapy
- Carcinoma
- Epidermal growth factor (EGF)
- Metastasis
- Network
- Receptor tyrosine kinase
- Signal transduction
- Transcription
All Science Journal Classification (ASJC) codes
- General Medicine
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