Non-Small Cell Lung Cancer Targeted Therapy: Drugs and Mechanisms of Drug Resistance.
Jiajia WuZhenghong LinPublished in: International journal of molecular sciences (2022)
The advent of precision medicine has brought light to the treatment of non-small cell lung cancer (NSCLC), expanding the options for patients with advanced NSCLC by targeting therapy through genetic and epigenetic cues. Tumor driver genes in NSCLC patients have been uncovered one by one, including epidermal growth factor receptor (EGFR), mesenchymal lymphoma kinase (ALK), and receptor tyrosine kinase ROS proto-oncogene 1 (ROS1) mutants. Antibodies and inhibitors that target the critical gene-mediated signaling pathways that regulate tumor growth and development are anticipated to increase patient survival and quality of life. Targeted drugs continue to emerge, with as many as two dozen approved by the FDA, and chemotherapy and targeted therapy have significantly improved patient prognosis. However, resistance due to cancer drivers' genetic alterations has given rise to significant challenges in treating patients with metastatic NSCLC. Here, we summarized the main targeted therapeutic sites of NSCLC drugs and discussed their resistance mechanisms, aiming to provide new ideas for follow-up research and clues for the improvement of targeted drugs.
Keyphrases
- epidermal growth factor receptor
- advanced non small cell lung cancer
- tyrosine kinase
- small cell lung cancer
- genome wide
- cancer therapy
- end stage renal disease
- dna methylation
- case report
- copy number
- signaling pathway
- stem cells
- ejection fraction
- newly diagnosed
- gene expression
- bone marrow
- peritoneal dialysis
- brain metastases
- diffuse large b cell lymphoma
- papillary thyroid
- squamous cell
- oxidative stress
- patient reported outcomes
- locally advanced
- squamous cell carcinoma
- binding protein
- lymph node metastasis
- pi k akt
- induced apoptosis
- endoplasmic reticulum stress
- young adults