The Pro-Survival Oct4/Stat1/Mcl-1 Axis Is Associated with Poor Prognosis in Lung Adenocarcinoma Patients.
Yu-Chu SuYi-Cheng ChenYau-Lin TsengGia-Shing ShiehPensee WuAi-Li ShiauChao-Liang WuPublished in: Cells (2021)
The embryonic stem cell marker Oct4 is expressed in several human cancers and is positively correlated with a poor outcome in cancer patients. However, its physiological role in cancer progression remains poorly understood. Tumor cells block apoptosis to escape cell death so that they can proliferate indefinitely, leading to ineffective therapy for cancer patients. In this study, we investigated whether Oct4 regulates the apoptosis pathway and contributes to poor prognosis in patients with lung adenocarcinoma. Our results revealed that Oct4 expression is correlated with Stat1 expression in lung adenocarcinoma patients and Oct4 is directly bound to the Stat1 promoter to transactivate Stat1 in lung adenocarcinoma cells. Expression of the Stat1 downstream gene Mcl-1 increased in Oct4-overexpressing cancer cells, while Stat1 knockdown in Oct4-overexpressing cancer cells sensitized them to cisplatin-induced apoptosis. Furthermore, Oct4 promoted Stat1 expression and tumor growth, whereas silencing of Stat1 reduced Oct4-induced tumor growth in human lung tumor xenograft models. Taken together, we demonstrate that Oct4 is a pro-survival factor by inducing Stat1 expression and that the Oct4/Stat1/Mcl-1 axis may be a potential therapeutic target for lung adenocarcinoma.
Keyphrases
- poor prognosis
- optical coherence tomography
- long non coding rna
- diabetic retinopathy
- induced apoptosis
- cell proliferation
- cell death
- endoplasmic reticulum stress
- optic nerve
- end stage renal disease
- stem cells
- cell cycle arrest
- oxidative stress
- newly diagnosed
- chronic kidney disease
- ejection fraction
- endothelial cells
- peritoneal dialysis
- risk assessment
- dna methylation
- single cell
- transcription factor
- squamous cell carcinoma
- high resolution
- patient reported outcomes
- lymph node metastasis
- high glucose
- pluripotent stem cells