<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>Yasinska, Inna M.</dc:creator>
  <dc:creator>Sakhnevych, Svetlana S.</dc:creator>
  <dc:creator>Pavlova, Ludmila</dc:creator>
  <dc:creator>Hansen Selnø, Anette Teo</dc:creator>
  <dc:creator>Teuscher Abeleira, Ana Maria</dc:creator>
  <dc:creator>Benlaouer, Ouafa</dc:creator>
  <dc:creator>Gonçalves Silva, Isabel</dc:creator>
  <dc:creator>Mosimann, Marianne</dc:creator>
  <dc:creator>Varani, Luca</dc:creator>
  <dc:creator>Bardelli, Marco</dc:creator>
  <dc:creator>Hussain, Rohanah</dc:creator>
  <dc:creator>Siligardi, Giuliano</dc:creator>
  <dc:creator>Cholewa, Dietmar</dc:creator>
  <dc:creator>Berger, Steffen M.</dc:creator>
  <dc:creator>Gibbs, Bernhard F.</dc:creator>
  <dc:creator>Ushkaryov, Yuri A.</dc:creator>
  <dc:creator>Fasler-Kan, Elizaveta</dc:creator>
  <dc:creator>Klenova, Elena</dc:creator>
  <dc:creator>Sumbayev, Vadim V.</dc:creator>
  <dc:date>2019-07-11</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Human cancer cells operate a variety of effective molecular and signaling mechanisms  which allow them to escape host immune surveillance and thus progress the disease. We  have recently reported that the immune receptor Tim-3 and its natural ligand galectin-9 are  involved in the immune escape of human acute myeloid leukemia (AML) cells. These cells  use the neuronal receptor latrophilin 1 (LPHN1) and its ligand fibronectin leucine rich  transmembrane protein 3 (FLRT3, and possibly other ligands) to trigger the pathway. We  hypothesized that the Tim-3-galectin-9 pathway may be involved in the immune escape of  cancer cells of different origins. We found that studied breast tumors expressed significantly  higher levels of both galectin-9 and Tim-3 compared to healthy breast tissues of the same  patients and that these proteins were co-localized. Increased levels of LPHN2 and  expressions of LPHN3 as well as FLRT3 were also detected in breast tumor cells.  Activation of this pathway facilitated the translocation of galectin-9 onto the tumor cell  surface, however no secretion of galectin-9 by tumor cells was observed. Surface-based  galectin-9 was able to protect breast carcinoma cells against cytotoxic T cell-induced death.  Furthermore, we found that cell lines from brain, colorectal, kidney, blood/mast cell, liver,  prostate, lung, and skin cancers expressed detectable amounts of both Tim-3 and galectin- 9 proteins. The majority of cell lines expressed one of the LPHN isoforms and FLRT3. We  conclude that the Tim-3-galectin-9 pathway is operated by a wide range of human cancer  cells and is possibly involved in prevention of anti-tumor immunity.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319080</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/319080</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319080/files/Yasinska_FrontImmunol_2019.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2019.01594</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319080</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Frontiers in immunology. - 2019, vol. 10, p. 1594</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Galectin-9</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">TIM-3</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Breast cancer</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Immune evasion</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Immune surveillance</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/616</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">The Tim-3-Galectin-9 Pathway and Its Regulatory Mechanisms in Human Breast Cancer</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
