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          <dc:identifier>https://hdl.handle.net/2286/R.2.N.164992</dc:identifier>
                  <dc:rights>http://rightsstatements.org/vocab/InC/1.0/</dc:rights>
          <dc:rights>http://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
                  <dc:date>2022-05</dc:date>
                  <dc:contributor>Cook, Margaret</dc:contributor>
          <dc:contributor>Plaisier, Christopher</dc:contributor>
          <dc:contributor>Plaisier, Christopher</dc:contributor>
          <dc:contributor>Wilson, Melissa</dc:contributor>
          <dc:contributor>Barrett, The Honors College</dc:contributor>
          <dc:contributor>Harrington Bioengineering Program</dc:contributor>
          <dc:contributor>School of Molecular Sciences</dc:contributor>
                  <dc:type>Text</dc:type>
                  <dc:description>&lt;p&gt;An immune regulatory network was constructed for the purpose of identifying target regulators in malignant pleural mesothelioma for therapies. An identified causal flow linked a mutation of D-dopachrome tautomerase to a heightened expression of regulator ASH1L and consequent down regulation of chemokine CCL5 and invasion of CD8+ T cells. Experimental validation of this initial use case indicates mRNA expression of CCL5 within the tumor cells and subsequent protein expression and secretion. Further analyses will explore the migration of CD8+ T cells in response to the chemotactic CCL5.&lt;/p&gt;
</dc:description>
                  <dc:subject>mesothelioma</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>immune</dc:subject>
          <dc:subject>Systems Biology</dc:subject>
                  <dc:title>Applying Regulatory Networks to the Immune Landscape of Mesothelioma</dc:title></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>
