GTSE1 promotes the growth of NSCLC by regulating microtubule-associated proteins through the ERK/MAPK pathway.
Chuanlin WangMeiyan WenJiali XuPengning GaoShanling LiuJiayu LiuYing ChenLan ZhouPublished in: Thoracic cancer (2023)
The role of G2 and S phase-expressed-1 (GTSE1), a microtubule-localized protein, in non-small-cell lung cancer (NSCLC) remains unknown. We explored its role in NSCLC growth. GTSE1 was detected in NSCLC tissues and cell lines using quantitative real-time polymerase chain reaction. The clinical significance of GTSE1 levels was evaluated. Biological and apoptotic effects of GTSE1 were evaluated using transwell, cell-scratch, and MTT assays, and flow cytometry and western blotting, respectively. Its association with cellular microtubules was shown by western blotting and immunofluorescence. GTSE1 expression was upregulated in NSCLC tissues and cell lines. GTSE1 levels correlated with lymph node metastasis. Higher GTSE1 mRNA expression correlated with shorter progression-free survival. GTSE1-knockdown decreased proliferation, colony formation, invasion, and migration of NSCLC cells, and inhibited tau and stathmin-1 microtubule-associated protein expression, via the extracellular-regulated protein kinase/mitogen-activated protein kinase (ERK/MAPK) signaling pathway, and microtubule disruption. GTSE1 may promote NSCLC growth by regulating tau and stathmin-1 through the ERK/MAPK signaling pathway.
Keyphrases
- signaling pathway
- small cell lung cancer
- pi k akt
- induced apoptosis
- advanced non small cell lung cancer
- lymph node metastasis
- epithelial mesenchymal transition
- cell cycle arrest
- brain metastases
- flow cytometry
- protein kinase
- squamous cell carcinoma
- cell proliferation
- free survival
- south africa
- epidermal growth factor receptor
- oxidative stress
- mass spectrometry
- poor prognosis
- cell therapy
- cerebrospinal fluid
- bone marrow
- high throughput
- transcription factor
- binding protein
- cell death