The role of non-coding RNAs in drug resistance of oral squamous cell carcinoma and therapeutic potential.
Xiang MengQiu-Yue LouWen-Ying YangYue-Rong WangRan ChenLu WangTao XuLei ZhangPublished in: Cancer communications (London, England) (2021)
Oral squamous cell carcinoma (OSCC), the eighth most prevalent cancer in the world, arises from the interaction of multiple factors including tobacco, alcohol consumption, and betel quid. Chemotherapeutic agents such as cisplatin, 5-fluorouracil, and paclitaxel have now become the first-line options for OSCC patients. Nevertheless, most OSCC patients eventually acquire drug resistance, leading to poor prognosis. With the discovery and identification of non-coding RNAs (ncRNAs), the functions of dysregulated ncRNAs in OSCC development and drug resistance are gradually being widely recognized. The mechanisms of drug resistance of OSCC are intricate and involve drug efflux, epithelial-mesenchymal transition, DNA damage repair, and autophagy. At present, strategies to explore the reversal of drug resistance of OSCC need to be urgently developed. Nano-delivery and self-cellular drug delivery platforms are considered as effective strategies to overcome drug resistance due to their tumor targeting, controlled release, and consistent pharmacokinetic profiles. In particular, the combined application of new technologies (including CRISPR systems) opened up new horizons for the treatment of drug resistance of OSCC. Hence, this review explored emerging regulatory functions of ncRNAs in drug resistance of OSCC, elucidated multiple ncRNA-meditated mechanisms of drug resistance of OSCC, and discussed the potential value of drug delivery platforms using nanoparticles and self-cells as carriers in drug resistance of OSCC.
Keyphrases
- drug delivery
- poor prognosis
- dna damage
- end stage renal disease
- epithelial mesenchymal transition
- newly diagnosed
- chronic kidney disease
- long non coding rna
- ejection fraction
- cancer therapy
- prognostic factors
- alcohol consumption
- gene expression
- emergency department
- young adults
- signaling pathway
- dna repair
- small molecule
- cell death
- patient reported outcomes
- high throughput
- genome editing
- combination therapy
- childhood cancer