<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Pankaew S</submitter><funding>Canceropôle PACA</funding><funding>Agence Nationale de la Recherche</funding><funding>Horizon 2020 Framework Programme</funding><funding>Centre National de la Recherche Scientifique</funding><funding>Institut National de la Santé et de la Recherche Médicale</funding><pubmed_abstract>PTEN (Phosphatase and TENsin homolog) is a well-known tumor suppressor involved in numerous types of cancer, including T-cell acute lymphoblastic leukemia (T-ALL). In human, loss-of-function mutations of &lt;i>PTEN&lt;/i> are correlated to mature T-ALL expressing a T-cell receptor (TCR) at their cell surface. In accordance with human T-ALL, inactivation of &lt;i>Pten&lt;/i> gene in mouse thymocytes induces TCRαβ&lt;sup>+&lt;/sup> T-ALL development. Herein, we explored the functional interaction between TCRαβ signaling and PTEN. First, we performed single-cell RNA sequencing (scRNAseq) of PTEN-deficient and PTEN-proficient thymocytes. Bioinformatic analysis of our scRNAseq data showed that pathological Pten&lt;sup>del&lt;/sup> thymocytes express, as expected, &lt;i>Myc&lt;/i> transcript, whereas inference of pathway act</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>797244</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8847596</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Calcium Signaling Is Impaired in PTEN-Deficient T Cell Acute Lymphoblastic Leukemia.</pubmed_title><pmcid>PMC8847596</pmcid><pubmed_authors>Pankaew S</pubmed_authors><pubmed_authors>Nozais M</pubmed_authors><pubmed_authors>Remy E</pubmed_authors><pubmed_authors>Loosveld M</pubmed_authors><pubmed_authors>Potier D</pubmed_authors><pubmed_authors>Quessada J</pubmed_authors><pubmed_authors>Payet-Bornet D</pubmed_authors><pubmed_authors>Grosjean C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Calcium Signaling Is Impaired in PTEN-Deficient T Cell Acute Lymphoblastic Leukemia.</name><description>PTEN (Phosphatase and TENsin homolog) is a well-known tumor suppressor involved in numerous types of cancer, including T-cell acute lymphoblastic leukemia (T-ALL). In human, loss-of-function mutations of &lt;i>PTEN&lt;/i> are correlated to mature T-ALL expressing a T-cell receptor (TCR) at their cell surface. In accordance with human T-ALL, inactivation of &lt;i>Pten&lt;/i> gene in mouse thymocytes induces TCRαβ&lt;sup>+&lt;/sup> T-ALL development. Herein, we explored the functional interaction between TCRαβ signaling and PTEN. First, we performed single-cell RNA sequencing (scRNAseq) of PTEN-deficient and PTEN-proficient thymocytes. Bioinformatic analysis of our scRNAseq data showed that pathological Pten&lt;sup>del&lt;/sup> thymocytes express, as expected, &lt;i>Myc&lt;/i> transcript, whereas inference of pathway act</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-31T02:07:19.829Z</modification><creation>2025-04-04T23:01:43.88Z</creation></dates><accession>S-EPMC8847596</accession><cross_references><pubmed>35185889</pubmed><doi>10.3389/fimmu.2022.797244</doi></cross_references></HashMap>