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Emerging roles and regulation of MiT/TFE transcriptional factors
- Source :
- Cell Communication and Signaling : CCS, Cell Communication and Signaling, Vol 16, Iss 1, Pp 1-11 (2018)
- Publication Year :
- 2018
- Publisher :
- BioMed Central, 2018.
-
Abstract
- The MiT/TFE transcription factors play a pivotal role in the regulation of autophagy and lysosomal biogenesis. The subcellular localization and activity of MiT/TFE proteins are primarily regulated through phosphorylation. And the phosphorylated protein is retained in the cytoplasm and subsequently translocates to the nucleus upon dephosphorylation, where it stimulates the expression of hundreds of genes, leading to lysosomal biogenesis and autophagy induction. The transcription factor-mediated lysosome-to-nucleus signaling can be directly controlled by several signaling molecules involved in the mTORC1, PKC, and AKT pathways. MiT/TFE family members have attracted much attention owing to their intracellular clearance of pathogenic factors in numerous diseases. Recently, multiple studies have also revealed the MiT/TFE proteins as master regulators of cellular metabolic reprogramming, converging on autophagic and lysosomal function and playing a critical role in cancer, suggesting that novel therapeutic strategies could be based on the modulation of MiT/TFE family member activity. Here, we present an overview of the latest research on MiT/TFE transcriptional factors and their potential mechanisms in cancer.
- Subjects :
- 0301 basic medicine
Cell signaling
lcsh:Medicine
mTORC1
Review
Biochemistry
03 medical and health sciences
Lysosome
medicine
Autophagy
Animals
Humans
lcsh:QH573-671
Molecular Biology
Transcription factor
Protein kinase B
MiT/TFE family
Cancer
TFEB
Microphthalmia-Associated Transcription Factor
lcsh:Cytology
Chemistry
lcsh:R
Autophagosomes
Cell Biology
Cell biology
TFE3
030104 developmental biology
medicine.anatomical_structure
Phosphorylation
Lysosomes
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 1478811X
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Cell Communication and Signaling : CCS
- Accession number :
- edsair.doi.dedup.....8b501bc76a6efb574ff6a5ba151251bb