Abstract
The Met proto-oncogene encodes MET tyrosine kinase protein which is a receptor for hepatocyte growth factor/scatter factor (HGF/SF). HGF binds to and activates MET to regulate diversified cellular and molecular activities such as proliferation, motility, differentiation, and survival. Aberration of HGF/MET signaling plays a proven role in promoting cancer initiation and malignant progression, providing a strong rationale for targeting the MET signaling pathway in the treatment of cancer. Several anti-HGF and anti-MET monoclonal antibodies, as well as small-molecule inhibitors of MET, are being evaluated in clinical trials for the treatment of various cancers. In this chapter, we discuss the role of HGF/MET signaling in cancer development and progression, the strategies for targeting MET signaling, as well as the promises and challenges of MET-targeted therapeutics.
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Acknowledgment
We thank Dr. Robert Wondergem for critical reading. This work is supported by Stephen M. Coffman Charitable Trust and ETSU Start-up Fund (Q. X.).
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Thewke, D.P., Kou, J., Fulmer, M.L., Xie, Q. (2018). The HGF/MET Signaling and Therapeutics in Cancer. In: Shinomiya, N., Kataoka, H., Xie, Q. (eds) Regulation of Signal Transduction in Human Cell Research. Current Human Cell Research and Applications. Springer, Singapore. https://doi.org/10.1007/978-981-10-7296-3_8
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