FHL1 promotes glioblastoma aggressiveness through regulating EGFR expression.
Lili SunLili ChenHua ZhuYumo LiClark C ChenMing LiPublished in: FEBS letters (2020)
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.
Keyphrases
- epidermal growth factor receptor
- tyrosine kinase
- small cell lung cancer
- advanced non small cell lung cancer
- transcription factor
- cell proliferation
- signaling pathway
- poor prognosis
- binding protein
- induced apoptosis
- endothelial cells
- squamous cell carcinoma
- computed tomography
- papillary thyroid
- risk assessment
- resting state
- white matter
- long non coding rna
- cell cycle arrest
- functional connectivity
- pi k akt
- combination therapy
- brain injury
- climate change
- replacement therapy
- multiple sclerosis
- squamous cell
- childhood cancer
- pluripotent stem cells