Lessons To Be Learned: The Molecular Basis of Kinase-Targeted Therapies and Drug Resistance in Non-Small Cell Lung Cancer
- PMID: 29178586
- DOI: 10.1002/anie.201710398
Lessons To Be Learned: The Molecular Basis of Kinase-Targeted Therapies and Drug Resistance in Non-Small Cell Lung Cancer
Abstract
The treatment of non-small cell lung cancer (NSCLC) is currently experiencing a revolution. Over the last decade, the knowledge gained about the biochemical features of biomarkers and their predictive abilities has led to the development of targeted small-molecule inhibitors that present an alternative to harsh chemotherapy. The use of these new therapies has improved the quality of life and increased the survival of patients. The occurrence of inevitable drug resistance requires the constant development of precision medicine. The detailed understanding of the target biology and the search for innovative chemical approaches has encouraged investigations in this field. Herein, we review selected aspects of the molecular targets and present an overview of current topics and challenges in the rational development of small molecules to target NSCLC.
Keywords: cancer; drug resistance; structural biology; targeted therapy; tyrosine kinases.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Similar articles
-
The function and therapeutic targeting of anaplastic lymphoma kinase (ALK) in non-small cell lung cancer (NSCLC).Mol Cancer. 2018 Feb 19;17(1):52. doi: 10.1186/s12943-018-0810-4. Mol Cancer. 2018. PMID: 29455675 Free PMC article. Review.
-
Overcoming resistance in non-small-cell lung cancer: A practical lesson for the medicinal chemist.Arch Pharm (Weinheim). 2018 Oct;351(10):e1800037. doi: 10.1002/ardp.201800037. Epub 2018 Aug 12. Arch Pharm (Weinheim). 2018. PMID: 30101528 Review.
-
Challenges in ALK inhibition of ALK-positive non-small-cell lung cancer: from ALK positivity detection to treatment strategies after relapse.Future Oncol. 2018 Sep;14(22):2303-2317. doi: 10.2217/fon-2018-0066. Epub 2018 Aug 8. Future Oncol. 2018. PMID: 30088419 Review.
-
Development of a Brigatinib degrader (SIAIS117) as a potential treatment for ALK positive cancer resistance.Eur J Med Chem. 2020 May 1;193:112190. doi: 10.1016/j.ejmech.2020.112190. Epub 2020 Feb 29. Eur J Med Chem. 2020. PMID: 32179332
-
Refining precision cancer therapy in ALK-positive NSCLC.EBioMedicine. 2019 Mar;41:9-10. doi: 10.1016/j.ebiom.2019.01.059. Epub 2019 Feb 6. EBioMedicine. 2019. PMID: 30737082 Free PMC article. No abstract available.
Cited by
-
Structural and chemical insights into the covalent-allosteric inhibition of the protein kinase Akt.Chem Sci. 2019 Feb 13;10(12):3573-3585. doi: 10.1039/c8sc05212c. eCollection 2019 Mar 28. Chem Sci. 2019. PMID: 30996949 Free PMC article.
-
Concurrent Targeting of Potential Cancer Stem Cells Regulating Pathways Sensitizes Lung Adenocarcinoma to Standard Chemotherapy.Mol Cancer Ther. 2020 Oct;19(10):2175-2185. doi: 10.1158/1535-7163.MCT-20-0024. Epub 2020 Aug 26. Mol Cancer Ther. 2020. PMID: 32847981 Free PMC article.
-
Synergistic antitumor activity of low-dose c-Met tyrosine kinase inhibitor and sorafenib on human non-small cell lung cancer cells.Oncol Lett. 2018 Apr;15(4):5081-5086. doi: 10.3892/ol.2018.7933. Epub 2018 Feb 2. Oncol Lett. 2018. PMID: 29552141 Free PMC article.
-
Role and potential therapeutic value of histone methyltransferases in drug resistance mechanisms in lung cancer.Front Oncol. 2024 Mar 8;14:1376916. doi: 10.3389/fonc.2024.1376916. eCollection 2024. Front Oncol. 2024. PMID: 38525426 Free PMC article. Review.
-
Effect of silkworm peptide on inducting M1 type polarization and Th1 activation via TLR2-induced MyD88-dependent pathway.Food Sci Nutr. 2019 Mar 12;7(4):1251-1260. doi: 10.1002/fsn3.954. eCollection 2019 Apr. Food Sci Nutr. 2019. PMID: 31024698 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous