<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cervero-Garcia P</submitter><funding>Blood Cancer UK</funding><pagination>vdag001</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12932952</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>TAT-Cx43&lt;sub>266-283&lt;/sub> is a novel Src inhibitor, which has shown noteworthy antitumor effects in preclinical models of glioblastoma. Because Src plays a pivotal role in several tumor types, including lung cancer brain metastasis derived from non-small cell lung cancer (NSCLC) cells, we investigated the effect of TAT-Cx43&lt;sub>266-283&lt;/sub> in NSCLC-derived brain metastasis, a disease of unmet clinical need.&lt;h4>Methods&lt;/h4>The effect of TAT-Cx43&lt;sub>266-283&lt;/sub> was studied in Lewis Lung Carcinoma (LLC), LSZ4, A549, and H441 NSCLC cells. The non-adherent stem-like LLC cells (LLC-CSCs) were intracranially implanted in immunocompetent mice to study the effect of TAT-Cx43&lt;sub>266-283&lt;/sub>  &lt;i>in vivo&lt;/i>. Phosphoproteomic analysis was employed to identify signaling path</pubmed_abstract><journal>Neuro-oncology advances</journal><pubmed_title>The Src inhibitor peptide TAT-Cx43&amp;lt;sub&amp;gt;266-283&amp;lt;/sub&amp;gt; improves survival in an intracranial murine model of lung cancer brain metastasis.</pubmed_title><pmcid>PMC12932952</pmcid><funding_grant_id>20008</funding_grant_id><pubmed_authors>Hijazi M</pubmed_authors><pubmed_authors>Rodrigues-Teixeira T</pubmed_authors><pubmed_authors>Alvarez-Vazquez A</pubmed_authors><pubmed_authors>Alonso-Amador JJ</pubmed_authors><pubmed_authors>Ollauri-Ibanez C</pubmed_authors><pubmed_authors>Martin-Guerrero SM</pubmed_authors><pubmed_authors>Cutillas PR</pubmed_authors><pubmed_authors>Casado P</pubmed_authors><pubmed_authors>Garcia-Guerrero L</pubmed_authors><pubmed_authors>Shields T</pubmed_authors><pubmed_authors>Flores-Hernandez R</pubmed_authors><pubmed_authors>Talaveron R</pubmed_authors><pubmed_authors>Tabernero A</pubmed_authors><pubmed_authors>Rajeeve V</pubmed_authors><pubmed_authors>Cervero-Garcia P</pubmed_authors><pubmed_authors>Jimenez-Madrona E</pubmed_authors><pubmed_authors>Paniagua-Sancho M</pubmed_authors><pubmed_authors>Jaraiz-Rodriguez M</pubmed_authors><pubmed_authors>Gonzalez-Sanchez R</pubmed_authors><pubmed_authors>Garcia-Vicente L</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Src inhibitor peptide TAT-Cx43&amp;lt;sub&amp;gt;266-283&amp;lt;/sub&amp;gt; improves survival in an intracranial murine model of lung cancer brain metastasis.</name><description>&lt;h4>Background&lt;/h4>TAT-Cx43&lt;sub>266-283&lt;/sub> is a novel Src inhibitor, which has shown noteworthy antitumor effects in preclinical models of glioblastoma. Because Src plays a pivotal role in several tumor types, including lung cancer brain metastasis derived from non-small cell lung cancer (NSCLC) cells, we investigated the effect of TAT-Cx43&lt;sub>266-283&lt;/sub> in NSCLC-derived brain metastasis, a disease of unmet clinical need.&lt;h4>Methods&lt;/h4>The effect of TAT-Cx43&lt;sub>266-283&lt;/sub> was studied in Lewis Lung Carcinoma (LLC), LSZ4, A549, and H441 NSCLC cells. The non-adherent stem-like LLC cells (LLC-CSCs) were intracranially implanted in immunocompetent mice to study the effect of TAT-Cx43&lt;sub>266-283&lt;/sub>  &lt;i>in vivo&lt;/i>. Phosphoproteomic analysis was employed to identify signaling path</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan-Dec</publication><modification>2026-07-14T09:22:02.553Z</modification><creation>2026-07-14T03:04:15.919Z</creation></dates><accession>S-EPMC12932952</accession><cross_references><pubmed>41756757</pubmed><doi>10.1093/noajnl/vdag001</doi></cross_references></HashMap>