Receptor Tyrosine Kinases in Osteosarcoma: 2019 Update

dc.contributor.authorGreenfield, Edward M.
dc.contributor.authorCollier, Christopher D.
dc.contributor.authorGetty, Patrick J.
dc.contributor.departmentOrthopaedic Surgery, School of Medicineen_US
dc.date.accessioned2022-03-04T21:51:07Z
dc.date.available2022-03-04T21:51:07Z
dc.date.issued2020
dc.description.abstractThe primary conclusions of our 2014 contribution to this series were as follows: Multiple receptor tyrosine kinases (RTKs) likely contribute to aggressive phenotypes in osteosarcoma and, therefore, inhibition of multiple RTKs is likely necessary for successful clinical outcomes. Inhibition of multiple RTKs may also be useful to overcome resistance to inhibitors of individual RTKs as well as resistance to conventional chemotherapies. Different combinations of RTKs are likely important in individual patients. AXL, EPHB2, FGFR2, IGF1R, and RET were identified as promising therapeutic targets by our in vitro phosphoproteomic/siRNA screen of 42 RTKs in the highly metastatic LM7 and 143B human osteosarcoma cell lines. This chapter is intended to provide an update on these topics as well as the large number of osteosarcoma clinical studies of inhibitors of multiple tyrosine kinases (multi-TKIs) that were recently published.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationGreenfield, E. M., Collier, C. D., & Getty, P. J. (2020). Receptor Tyrosine Kinases in Osteosarcoma: 2019 Update. Advances in Experimental Medicine and Biology, 1258, 141–155. https://doi.org/10.1007/978-3-030-43085-6_9en_US
dc.identifier.urihttps://hdl.handle.net/1805/28059
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/978-3-030-43085-6_9en_US
dc.relation.journalAdvances in Experimental Medicine and Biologyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectosteosarcomaen_US
dc.subjectreceptor tyrosine kinasesen_US
dc.subjectmulti-TKIsen_US
dc.titleReceptor Tyrosine Kinases in Osteosarcoma: 2019 Updateen_US
dc.typeArticleen_US
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