<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(8)</volume><submitter>Buglioni S</submitter><pubmed_abstract>Whether PD-L1 expression is associated with survival outcomes in gastric cancer (GC) is controversial. The inhibition of the PD-1/PD-L1 pathway is effective against genomically unstable tumors. Hypothesizing that also the clinical significance of PD-L1 might be dependent on the activation of molecular circuits ensuring genomic stability, we evaluated PD-L1 expression in tissue samples from 72 advanced GC patients treated with first-line chemotherapy. Samples were already characterized for DNA damage repair (DDR) component expression (pATM, pChk1, pWee1, γ-H2AX and pRPA2) along with mutations in DDR-linked genes (&lt;i>TP53&lt;/i> and &lt;i>ARID1A&lt;/i>). Overall, PD-L1 expression was not associated with progression-free survival (PFS) and overall survival (OS), independently on whether we considered </pubmed_abstract><journal>Oncoimmunology</journal><pagination>e1457602</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6136851</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The clinical significance of PD-L1 in advanced gastric cancer is dependent on &lt;i>ARID1A&lt;/i> mutations and ATM expression.</pubmed_title><pmcid>PMC6136851</pmcid><pubmed_authors>Buglioni S</pubmed_authors><pubmed_authors>Diodoro MG</pubmed_authors><pubmed_authors>Ciliberto G</pubmed_authors><pubmed_authors>Fanciulli M</pubmed_authors><pubmed_authors>Barba M</pubmed_authors><pubmed_authors>Pescarmona E</pubmed_authors><pubmed_authors>Sperati F</pubmed_authors><pubmed_authors>Maugeri-Sacca M</pubmed_authors><pubmed_authors>Goeman F</pubmed_authors><pubmed_authors>Vitale I</pubmed_authors><pubmed_authors>De Maria R</pubmed_authors><pubmed_authors>De Nicola F</pubmed_authors><pubmed_authors>Terrenato I</pubmed_authors><pubmed_authors>Pizzuti L</pubmed_authors><pubmed_authors>Di Lauro L</pubmed_authors><pubmed_authors>Casini B</pubmed_authors><pubmed_authors>Sergi D</pubmed_authors><pubmed_authors>Melucci E</pubmed_authors><pubmed_authors>Amoreo CA</pubmed_authors><pubmed_authors>Pallocca M</pubmed_authors><pubmed_authors>Mazzotta M</pubmed_authors><pubmed_authors>Gallo E</pubmed_authors><pubmed_authors>Vici P</pubmed_authors></additional><is_claimable>false</is_claimable><name>The clinical significance of PD-L1 in advanced gastric cancer is dependent on &lt;i>ARID1A&lt;/i> mutations and ATM expression.</name><description>Whether PD-L1 expression is associated with survival outcomes in gastric cancer (GC) is controversial. The inhibition of the PD-1/PD-L1 pathway is effective against genomically unstable tumors. Hypothesizing that also the clinical significance of PD-L1 might be dependent on the activation of molecular circuits ensuring genomic stability, we evaluated PD-L1 expression in tissue samples from 72 advanced GC patients treated with first-line chemotherapy. Samples were already characterized for DNA damage repair (DDR) component expression (pATM, pChk1, pWee1, γ-H2AX and pRPA2) along with mutations in DDR-linked genes (&lt;i>TP53&lt;/i> and &lt;i>ARID1A&lt;/i>). Overall, PD-L1 expression was not associated with progression-free survival (PFS) and overall survival (OS), independently on whether we considered </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-04T10:18:42.366Z</modification><creation>2019-06-06T22:45:52Z</creation></dates><accession>S-EPMC6136851</accession><cross_references><pubmed>30221053</pubmed><doi>10.1080/2162402x.2018.1457602</doi><doi>10.1080/2162402X.2018.1457602</doi></cross_references></HashMap>