<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Veltri G</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><funding>Fondazione Cassa di Risparmio di Padova e Rovigo</funding><funding>Fondazione Umberto Veronesi</funding><funding>Associazione Italiana Contro le Leucemie-Linfomi e Mieloma</funding><funding>Associazione Italiana per la ricerca sul cancro</funding><funding>Fondazione Città della Speranza Istituto di Ricerca Pediatrica</funding><funding>progetti di rilevante interesse nazionale</funding><pagination>3724</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8345121</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(15)</volume><pubmed_abstract>Lymphoblastic lymphoma (LBL) is the second most common type of non-Hodgkin lymphoma in childhood, mainly of T cell origin (T-LBL). Although current treatment protocols allow a complete remission in 85% of cases, the second-line treatment overall survival for patients with progressive or relapsed disease is around 14%, making this the major issue to be confronted. Thus, we performed a Reverse Phase Protein Array study in a cohort of 22 T-LBL patients to find reliable disease risk marker(s) and new therapeutic targets to improve pediatric T-LBL patients' outcome. Interestingly, we pinpointed JAK2 Y1007-1008 as a potential prognosis marker as well as a therapeutic target in poor prognosis patients. Hence, the hyperactivation of the JAK1/2-STAT6 pathway characterizes these latter patients. Mor</pubmed_abstract><journal>Cancers</journal><pubmed_title>Ruxolitinib as a Novel Therapeutic Option for Poor Prognosis T-LBL Pediatric Patients.</pubmed_title><pmcid>PMC8345121</pmcid><funding_grant_id>19/08</funding_grant_id><funding_grant_id>17/07_1FCR</funding_grant_id><funding_grant_id>21771</funding_grant_id><funding_grant_id>20178S4EK9</funding_grant_id><funding_grant_id>AIL-TV</funding_grant_id><funding_grant_id>19186</funding_grant_id><funding_grant_id>2064</funding_grant_id><pubmed_authors>Gallingani I</pubmed_authors><pubmed_authors>Serafin V</pubmed_authors><pubmed_authors>Veltri G</pubmed_authors><pubmed_authors>Mussolin L</pubmed_authors><pubmed_authors>Bresolin S</pubmed_authors><pubmed_authors>Lovisa F</pubmed_authors><pubmed_authors>Carraro E</pubmed_authors><pubmed_authors>Vencato S</pubmed_authors><pubmed_authors>Sandei M</pubmed_authors><pubmed_authors>Biffi A</pubmed_authors><pubmed_authors>Accordi B</pubmed_authors><pubmed_authors>Pillon M</pubmed_authors><pubmed_authors>Silvestri C</pubmed_authors><pubmed_authors>Cortese G</pubmed_authors><pubmed_authors>Basso G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ruxolitinib as a Novel Therapeutic Option for Poor Prognosis T-LBL Pediatric Patients.</name><description>Lymphoblastic lymphoma (LBL) is the second most common type of non-Hodgkin lymphoma in childhood, mainly of T cell origin (T-LBL). Although current treatment protocols allow a complete remission in 85% of cases, the second-line treatment overall survival for patients with progressive or relapsed disease is around 14%, making this the major issue to be confronted. Thus, we performed a Reverse Phase Protein Array study in a cohort of 22 T-LBL patients to find reliable disease risk marker(s) and new therapeutic targets to improve pediatric T-LBL patients' outcome. Interestingly, we pinpointed JAK2 Y1007-1008 as a potential prognosis marker as well as a therapeutic target in poor prognosis patients. Hence, the hyperactivation of the JAK1/2-STAT6 pathway characterizes these latter patients. Mor</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-04-08T07:48:02.646Z</modification><creation>2022-02-11T05:45:52.51Z</creation></dates><accession>S-EPMC8345121</accession><cross_references><pubmed>34359628</pubmed><doi>10.3390/cancers13153724</doi></cross_references></HashMap>