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NSCLC: from tumorigenesis, immune checkpoint misuse to current and future targeted therapy
L. Raskova Kafkova, JM. Mierzwicka, P. Chakraborty, P. Jakubec, O. Fischer, J. Skarda, P. Maly, M. Raska
Language English Country Switzerland
Document type Journal Article, Review, Research Support, Non-U.S. Gov't
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- MeSH
- B7-H1 Antigen metabolism MeSH
- ErbB Receptors metabolism MeSH
- Phosphatidylinositol 3-Kinases metabolism MeSH
- Carcinogenesis MeSH
- Humans MeSH
- Cell Transformation, Neoplastic MeSH
- Lung Neoplasms * drug therapy genetics MeSH
- Carcinoma, Non-Small-Cell Lung * drug therapy genetics MeSH
- Proto-Oncogene Proteins p21(ras) MeSH
- Receptor Protein-Tyrosine Kinases metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Non-small cell lung cancer (NSCLC) is largely promoted by a multistep tumorigenesis process involving various genetic and epigenetic alterations, which essentially contribute to the high incidence of mortality among patients with NSCLC. Clinical observations revealed that NSCLC also co-opts a multifaceted immune checkpoint dysregulation as an important driving factor in NSCLC progression and development. For example, a deregulated PI3K/AKT/mTOR pathway has been noticed in 50-70% of NSCLC cases, primarily modulated by mutations in key oncogenes such as ALK, EGFR, KRAS, and others. Additionally, genetic association studies containing patient-specific factors and local reimbursement criteria expose/reveal mutations in EGFR/ALK/ROS/BRAF/KRAS/PD-L1 proteins to determine the suitability of available immunotherapy or tyrosine kinase inhibitor therapy. Thus, the expression of such checkpoints on tumors and immune cells is pivotal in understanding the therapeutic efficacy and has been extensively studied for NSCLC treatments. Therefore, this review summarizes current knowledge in NSCLC tumorigenesis, focusing on its genetic and epigenetic intricacies, immune checkpoint dysregulation, and the evolving landscape of targeted therapies. In the context of current and future therapies, we emphasize the significance of antibodies targeting PD-1/PD-L1 and CTLA-4 interactions as the primary therapeutic strategy for immune system reactivation in NSCLC. Other approaches involving the promising potential of nanobodies, probodies, affibodies, and DARPINs targeting immune checkpoints are also described; these are under active research or clinical trials to mediate immune regulation and reduce cancer progression. This comprehensive review underscores the multifaceted nature, current state and future directions of NSCLC research and treatment.
Department of Immunology University Hospital Olomouc Olomouc Czechia
Department of Respiratory Diseases and Tuberculosis University Hospital Olomouc Olomouc Czechia
References provided by Crossref.org
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