Progress in Glioma Stem Cell Research.
Vanajothi RamarShanchun GuoBreAnna HudsonMingli LiuPublished in: Cancers (2023)
Glioblastoma multiforme (GBM) represents a diverse spectrum of primary tumors notorious for their resistance to established therapeutic modalities. Despite aggressive interventions like surgery, radiation, and chemotherapy, these tumors, due to factors such as the blood-brain barrier, tumor heterogeneity, glioma stem cells (GSCs), drug efflux pumps, and DNA damage repair mechanisms, persist beyond complete isolation, resulting in dismal outcomes for glioma patients. Presently, the standard initial approach comprises surgical excision followed by concurrent chemotherapy, where temozolomide (TMZ) serves as the foremost option in managing GBM patients. Subsequent adjuvant chemotherapy follows this regimen. Emerging therapeutic approaches encompass immunotherapy, including checkpoint inhibitors, and targeted treatments, such as bevacizumab, aiming to exploit vulnerabilities within GBM cells. Nevertheless, there exists a pressing imperative to devise innovative strategies for both diagnosing and treating GBM. This review emphasizes the current knowledge of GSC biology, molecular mechanisms, and associations with various signals and/or pathways, such as the epidermal growth factor receptor, PI3K/AKT/mTOR, HGFR/c-MET, NF-κB, Wnt, Notch, and STAT3 pathways. Metabolic reprogramming in GSCs has also been reported with the prominent activation of the glycolytic pathway, comprising aldehyde dehydrogenase family genes. We also discuss potential therapeutic approaches to GSC targets and currently used inhibitors, as well as their mode of action on GSC targets.
Keyphrases
- stem cells
- dna damage
- end stage renal disease
- epidermal growth factor receptor
- newly diagnosed
- ejection fraction
- chronic kidney disease
- cell proliferation
- peritoneal dialysis
- oxidative stress
- locally advanced
- tyrosine kinase
- minimally invasive
- induced apoptosis
- signaling pathway
- emergency department
- physical activity
- squamous cell carcinoma
- transcription factor
- skeletal muscle
- immune response
- genome wide
- cell cycle arrest
- rectal cancer
- acute coronary syndrome
- dna repair
- nuclear factor
- cell death
- patient reported
- weight loss
- inflammatory response
- lps induced
- endoplasmic reticulum stress
- adverse drug