دورية أكاديمية
Inhibition of the MET Kinase Activity and Cell Growth in MET-Addicted Cancer Cells by Bi-Paratopic Linking
العنوان: | Inhibition of the MET Kinase Activity and Cell Growth in MET-Addicted Cancer Cells by Bi-Paratopic Linking |
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المؤلفون: | Andres F., Iamele L., Meyer T., Stuber J. C., Kast F., Gherardi E., Niemann H. H., Pluckthun A. |
المساهمون: | Andres, F., Iamele, L., Meyer, T., Stuber, J. C., Kast, F., Gherardi, E., Niemann, H. H., Pluckthun, A. |
سنة النشر: | 2019 |
المجموعة: | IRIS UNIPV (Università degli studi di Pavia) |
مصطلحات موضوعية: | biparatopic, DARPin, MET, protein engineering, X-ray crystallography, Cell Line, Tumor, Cell Proliferation, Crystallography, X-Ray, Human, Models, Molecular, Neoplasm, Protein Kinase Inhibitor, Proto-Oncogene Proteins c-met, Recombinant Fusion Protein, Ankyrin Repeat |
الوصف: | MET, the product of the c-MET proto-oncogene, and its ligand hepatocyte growth factor/scatter factor (HGF/SF) control survival, proliferation and migration during development and tissue regeneration. HGF/SF-MET signaling is equally crucial for growth and metastasis of a variety of human tumors, but resistance to small-molecule inhibitors of MET kinase develops rapidly and therapeutic antibody targeting remains challenging. We made use of the designed ankyrin repeat protein (DARPin) technology to develop an alternative approach for inhibiting MET. We generated a collection of MET-binding DARPins covering epitopes in the extracellular MET domains and created comprehensive sets of bi-paratopic fusion proteins. This new class of molecules efficiently inhibited MET kinase activity and downstream signaling, caused receptor downregulation and strongly inhibited the proliferation of MET-dependent gastric carcinoma cells carrying MET locus amplifications. MET-specific bi-paratopic DARPins may represent a novel and potent strategy for therapeutic targeting of MET and other receptors, and this study has elucidated their mode of action. |
نوع الوثيقة: | article in journal/newspaper |
وصف الملف: | ELETTRONICO |
اللغة: | English |
العلاقة: | info:eu-repo/semantics/altIdentifier/pmid/30930049; info:eu-repo/semantics/altIdentifier/wos/WOS:000471087100009; volume:431; issue:10; firstpage:2020; lastpage:2039; numberofpages:20; journal:JOURNAL OF MOLECULAR BIOLOGY; http://hdl.handle.net/11571/1419215Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85064891161 |
DOI: | 10.1016/j.jmb.2019.03.024 |
الإتاحة: | https://doi.org/10.1016/j.jmb.2019.03.024Test http://hdl.handle.net/11571/1419215Test |
رقم الانضمام: | edsbas.8DF7FA5 |
قاعدة البيانات: | BASE |
DOI: | 10.1016/j.jmb.2019.03.024 |
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