International journal of molecular sciences, 2017-02, Vol.18 (3), p.482-482
2017
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- Autor(en) / Beteiligte
- Titel
- L1198F Mutation Resensitizes Crizotinib to ALK by Altering the Conformation of Inhibitor and ATP Binding Sites
- Ist Teil von
- International journal of molecular sciences, 2017-02, Vol.18 (3), p.482-482
- Ort / Verlag
- Switzerland: MDPI
- Erscheinungsjahr
- 2017
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- The efficacy of anaplastic lymphoma kinase (ALK) positive non-small-cell lung cancer (NSCLC) treatment with small molecule inhibitors is greatly challenged by acquired resistance. A recent study reported the newest generation inhibitor resistant mutation L1198F led to the resensitization to crizotinib, which is the first Food and Drug Administration (FDA) approved drug for the treatment of ALK-positive NSCLC. It is of great importance to understand how this extremely rare event occurred for the purpose of overcoming the acquired resistance of such inhibitors. In this study, we exploited molecular dynamics (MD) simulation to dissect the molecular mechanisms. Our MD results revealed that L1198F mutation of ALK resulted in the conformational change at the inhibitor site and altered the binding affinity of ALK to crizotinib and lorlatinib. L1198F mutation also affected the autoactivation of ALK as supported by the identification of His1124 and Tyr1278 as critical amino acids involved in ATP binding and phosphorylation. Our findings are valuable for designing more specific and potent inhibitors for the treatment of ALK-positive NSCLC and other types of cancer.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1422-0067eISSN: 1422-0067DOI: 10.3390/ijms18030482Titel-ID: cdi_doaj_primary_oai_doaj_org_article_60f60d1bc1d84d6ea35483a5f78a42b8
- Format
- –
- Schlagworte
- Adenosine Triphosphate - chemistry, Adenosine Triphosphate - metabolism, ALK, Amino Acids - chemistry, Binding Sites, Codon, drug resistance, Drug Resistance, Neoplasm - genetics, Humans, lorlatinib, Models, Molecular, Molecular Conformation, Mutation, point mutation, Protein Binding, Protein Interaction Domains and Motifs, Protein Kinase Inhibitors - chemistry, Protein Kinase Inhibitors - pharmacology, Pyrazoles - chemistry, Pyrazoles - pharmacology, Pyridines - chemistry, Pyridines - pharmacology, Receptor Protein-Tyrosine Kinases - antagonists & inhibitors, Receptor Protein-Tyrosine Kinases - chemistry, Receptor Protein-Tyrosine Kinases - genetics, resensitization, Structure-Activity Relationship