FHL1 promotes glioblastoma aggressiveness through regulating EGFR expression

FEBS Lett. 2021 Jan;595(1):85-98. doi: 10.1002/1873-3468.13955. Epub 2020 Oct 28.

Abstract

The four-and-a-half LIM domain protein 1 (FHL1) plays a key role in multiple cancers. Here, we characterized its role in glioblastoma (GBM), the most common and incurable form of brain cancer. Overexpression of FHL1 promotes growth, migration, and invasion of GBM cells in vivo and in vitro. In contrast, FHL1 silencing by RNAi exhibits the opposite effects. FHL1 interacts with the transcription factor SP1 to upregulate epidermal growth factor receptor (EGFR) expression and activate the downstream signaling cascades, including Src, Akt, Erk1/2, and Stat3, leading to GBM malignancy. FHL1 is highly expressed and positively correlated with EGFR levels in human GBM, particularly those of the classical subtype. Our results suggest that the FHL1-SP1-EGFR axis plays a tumor-promoting role, and highlight the translational potential of inhibiting FHL1 for GBM treatment.

Keywords: EGFR; FHL1; SP1; glioblastoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / pathology*
  • Cell Proliferation
  • Disease Progression
  • ErbB Receptors / physiology
  • Gene Silencing
  • Glioblastoma / pathology*
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Intracellular Signaling Peptides and Proteins / physiology*
  • LIM Domain Proteins / genetics
  • LIM Domain Proteins / metabolism
  • LIM Domain Proteins / physiology*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Muscle Proteins / physiology*
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Protein Kinases / metabolism
  • STAT2 Transcription Factor / metabolism
  • Sp1 Transcription Factor / metabolism

Substances

  • FHL1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • LIM Domain Proteins
  • Muscle Proteins
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • Sp1 Transcription Factor
  • Protein Kinases
  • EGFR protein, human
  • ErbB Receptors