<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Arcaro A</dc:creator>
  <dc:date>2013</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The insulin-like growth factor (IGF) signaling system plays a crucial role in human cancer and the IGF-1 receptor (IGF-1R) is an attractive drug target against which a variety of novel anti-tumor agents are being developed. Deregulation of the IGF signaling pathway frequently occurs in human cancer and involves the establishment of autocrine loops comprising IGF-1 or IGF-2 and/or IGF-1R over-expression. Epidemiologic studies have documented a link between elevated IGF levels and the development of solid tumors, such as breast, colon, and prostate cancer. Anti-cancer strategies targeting the IGF signaling system involve two main approaches, namely neutralizing antibodies and small molecule inhibitors of the IGF-1R kinase activity. There are numerous reports describing anti-tumor activity of these agents in pre-clinical models of major human cancers. In addition, multiple clinical trials have started to evaluate the safety and efficacy of selected IGF-1R inhibitors, in combination with standard chemotherapeutic regimens or other targeted agents in cancer patients. In this mini review, I will discuss the role of the IGF signaling system in human cancer and the main strategies which have been so far evaluated to target the IGF-1R.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/71355</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fphar.2013.00030</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/23525758</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Frontiers in pharmacology. - 2013</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">IGF-1 receptor</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">cancer</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">clinical trials</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">insulin-like growth factor</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">monoclonal antibody</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">tyrosine kinase inhibitor</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Targeting the insulin-like growth factor-1 receptor in human cancer.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
