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Molecular Dynamics Validation of Crizotinib Resistance to ALK Mutations (L1196M and G1269A) and Identification of Specific Inhibitors.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 2017 Oct; Vol. 118 (10), pp. 3462-3471. Date of Electronic Publication: 2017 May 18. - Publication Year :
- 2017
-
Abstract
- Anaplastic lymphoma kinase (ALK) positive non-small cell lung cancer (NSCLC) patients are mostly treated with ALK tyrosine kinase inhibitors (TKIs). Crizotinib is the first generation ALK inhibitor practiced as a primary chemo to combat cancer cells followed by second generation inhibitor ceritinib which are effective against crizotinib resistant ALK mutations. However, patients treated with these drugs invariably relapsed because of the development of new drug resistance mutations. In this study we explored the crizotinib resistance in the presence of ALK mutations L1196M and G1269A through molecular dynamics simulation studies. Further mutation specific inhibitors CID 71748211 and CID 71728095 were identified to potentially inhibit ALK with mutations L1196M and G1269A, respectively. This computational investigation in-sighted the molecular factors involved in crizotinib resistance which enhanced in the identification of new ALK drugs that brings individualized medicine to treat ALK positive NSCLC patients with specific mutations. J. Cell. Biochem. 118: 3462-3471, 2017. © 2017 Wiley Periodicals, Inc.<br /> (© 2017 Wiley Periodicals, Inc.)
- Subjects :
- Amino Acid Substitution
Anaplastic Lymphoma Kinase
Carcinoma, Non-Small-Cell Lung diet therapy
Carcinoma, Non-Small-Cell Lung genetics
Crizotinib
Humans
Lung Neoplasms drug therapy
Lung Neoplasms genetics
Receptor Protein-Tyrosine Kinases genetics
Carcinoma, Non-Small-Cell Lung enzymology
Drug Resistance, Neoplasm
Lung Neoplasms enzymology
Molecular Dynamics Simulation
Mutation, Missense
Protein Kinase Inhibitors chemistry
Pyrazoles chemistry
Pyridines chemistry
Receptor Protein-Tyrosine Kinases antagonists & inhibitors
Receptor Protein-Tyrosine Kinases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4644
- Volume :
- 118
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28332225
- Full Text :
- https://doi.org/10.1002/jcb.26004