Microphthalmia/Transcription Factor E (MiT/TFE) Pathways in Pulmonary Diseases: Current Evidence and Emerging

Priyanka Singh1, Evans Kwabena Abor1, Wei Shi1

  • 1Division of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.

Cells
|April 27, 2026
PubMed

Insights

MiT/TFE transcription factors regulate key cellular processes. Their dysregulation is linked to lung diseases like asthma and cancer, highlighting a need for further research into their role and therapeutic potential.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Pulmonary Medicine

Background:

  • MiT/TFE transcription factors are crucial for lysosomal biogenesis, autophagy, and lipid metabolism via the CLEAR gene network.
  • Dysregulation of MiT/TFE is implicated in cancer and neurodegeneration, but its role in pulmonary diseases is unclear.

Purpose of the Study:

  • To systematically review the role of MiT/TFE dysregulation in human pulmonary diseases.
  • To discuss MiT/TFE regulation pathways and identify research gaps.

Main Methods:

  • Systematic review of human pulmonary diseases and genetic disorders.
  • Analysis of MiT/TFE signaling pathways (e.g., mTORC1, AMPK, lysosomal stress).

Main Results:

  • MiT/TFE dysregulation is implicated in asthma, lung cancer, Birt-Hogg-Dube syndrome, and lung injury models.
  • Key regulatory pathways involving mTORC1, AMPK, and lysosomal stress were discussed.

Conclusions:

  • MiT/TFE signaling is relevant to various human lung diseases.
  • Further research, particularly in vivo models of combined TFEB/TFE3 activity, is needed for disease prevention and treatment.

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