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dc.contributor.authorShali, H
dc.contributor.authorAhmadi, M
dc.contributor.authorKafil, HS
dc.contributor.authorDorosti, A
dc.contributor.authorYousefi, M
dc.date.accessioned2018-08-26T07:26:22Z
dc.date.available2018-08-26T07:26:22Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46767
dc.description.abstractThe type 1 IGF receptor (IGF1R) and mesenchymal-epithelial transition (MET) are hetrodimeric and transmembrane receptor tyrosine kinases, which are frequently overexpressed by several tumor types, including colorectal cancer (CRC). These receptors bind to their specific ligands, insulin growth factors (IGFs) and hepatocyte growth factor (HGF), respectively, and promote signaling cascades which mediates many functions such as proliferation and protection against apoptosis, cell scattering, tumor cell motility, invasion and metastasis. In patients with metastatic colorectal cancer (mCRC), IGF1R and c-met expression confer resistance to cetuximab (monoclonal antibodies against EGFR). Therefore, the c-met and IGF1R are now an attractive novel target for anticancer therapy. In this review, we will describe correlation between two receptors and their activation effects in tumor cells, and finally introduce useful and available strategies for their targeting. (C) 2016 Elsevier Masson SAS. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofBIOMEDICINE & PHARMACOTHERAPY
dc.subjectColorectal cancer
dc.subjectIGF1R
dc.subjectc-Met
dc.subjectReceptor tyrosine kinase
dc.titleIGF1R and c-met as therapeutic targets for colorectal cancer
dc.typeReview
dc.citation.volume82
dc.citation.spage528
dc.citation.epage536
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.biopha.2016.05.034


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