The FOXO family of transcription factors: key molecular players in gastric cancer.
Ying LiuXiang AoYi JiaXiaoge LiYu WangJianxun WangPublished in: Journal of molecular medicine (Berlin, Germany) (2022)
Gastric cancer (GC) is the fifth most frequently diagnosed cancer worldwide and the third leading cause of cancer-related death with an oncological origin. Despite its decline in incidence and mortality in recent years, GC remains a global public problem that seriously threatens patients' health and lives. The forkhead box O proteins (FOXOs) are a family of evolutionarily conserved transcription factors (TFs) with crucial roles in cell fate decisions. In mammals, the FOXO family consists of four members FOXO1, 3a, 4, and 6. FOXOs play crucial roles in a variety of biological processes, such as development, metabolism, and stem cell maintenance, by regulating the expression of their target genes in space and time. An accumulating amount of evidence has shown that the dysregulation of FOXOs is involved in GC progression by affecting multiple cellular processes, including proliferation, apoptosis, invasion, metastasis, cell cycle progression, carcinogenesis, and resistance to chemotherapeutic drugs. In this review, we systematically summarize the recent findings on the regulatory mechanisms of FOXO family expression and activity and elucidate its roles in GC progression. Moreover, we also highlight the clinical implications of FOXOs in GC treatment.
Keyphrases
- transcription factor
- cell cycle
- genome wide identification
- dna binding
- gas chromatography
- poor prognosis
- stem cells
- healthcare
- cell fate
- signaling pathway
- cell proliferation
- ejection fraction
- mental health
- public health
- end stage renal disease
- risk factors
- newly diagnosed
- prostate cancer
- oxidative stress
- cell death
- genome wide
- squamous cell carcinoma
- prognostic factors
- papillary thyroid
- mass spectrometry
- health information
- cardiovascular events
- pi k akt
- combination therapy
- high resolution
- single molecule
- replacement therapy
- coronary artery disease
- long non coding rna
- radical prostatectomy
- squamous cell
- adverse drug
- cell migration
- bioinformatics analysis
- minimally invasive
- risk assessment
- health promotion