<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>Tarantelli, Chiara</dc:creator>
  <dc:creator>Lupia, Antonio</dc:creator>
  <dc:creator>Stathis, Anastasios</dc:creator>
  <dc:creator>Bertoni, Francesco</dc:creator>
  <dc:date>2020-02-05</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The activation of the PI3K/AKT/mTOR pathway is a main driver of cell growth, proliferation, survival, and  chemoresistance of cancer cells, and, for this reason, represents an attractive target for developing targeted anti- cancer drugs. There are plenty of preclinical data sustaining the anti-tumor activity of dual PI3K/mTOR inhibitors as  single agents and in combination in lymphomas. Clinical responses, including complete remissions (especially in  follicular lymphoma patients), are also observed in the very few clinical studies performed in patients that are affected  by relapsed/refractory lymphomas or chronic lymphocytic leukemia. In this review, we summarize the literature on  dual PI3K/mTOR inhibitors focusing on the lymphoma setting, presenting both the three compounds still in clinical  development and those with a clinical program stopped or put on hold.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/319051</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1319051</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319051/files/Bertoni_ijms_2020.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms21031060</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319051</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>International journal of molecular sciences. - 2020, vol. 21, no. 3, p. 21 p</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">TORC1</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">TORC2</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">PI3K</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Lymphoma</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Chronic lymphocytic leukemia</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Is there a role for dual PI3K/mTOR inhibitors for patients affected with lymphoma?</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
