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<dc:title xml:lang="en">Dual STAT3/STAT5 inhibition as a novel treatment strategy in T-prolymphocytic leukemia</dc:title>

  
<dc:description xml:lang="en">T-prolymphocytic leukemia (T-PLL) is a rare, aggressive T-cell malignancy with poor outcomes and an urgent need for new therapeutic approaches. Integrating genomic data and new transcriptomic profiling, we identified recurrent JAK/STAT mutations (predominantly in JAK3 and STAT5B) as hallmarks in a cohort of 335 T-PLL cases. In line, transcriptomic and protein analyses revealed constitutive JAK/STAT activation in virtually all samples. Consequently, we explored the anti-leukemic potential of dual STAT3/STAT5 non-PROTAC degraders in T-PLL, with JPX-1244 as our lead substance. JPX-1244 efficiently and selectively induced cell death in primary T-PLL samples, including those resistant to conventional therapies, by blocking STAT3 and STAT5 phosphorylation and by inducing their degradation. The extent of STAT3/STAT5 degradation directly correlated with cytotoxicity. RNA-sequencing confirmed the treatment-related downregulation of STAT5 target genes. While JAK/STAT mutations did not predict responses to pharmacologic STAT3/STAT5 degradation, elevated expression of TOX, PAK6, and SPINT1 were associated with drug sensitivity. In subsequent combination screenings, cladribine, venetoclax, and azacytidine emerged as most effective combination partners of STAT3/STAT5 degraders, even in low-responding T-PLL samples, all synergistically reducing STAT5 phosphorylation. These findings highlight dual STAT3/STAT5 inhibition, particularly in combination with hypomethylating and BCL2-targeting agents, as a promising interventional approach in T-PLL, warranting further investigation.</dc:description>

  
<dc:identifier rdf:resource="https://phaidra.vetmeduni.ac.at/o:4646"></dc:identifier>

  
<dc:language>en</dc:language>

  
<edm:type>TEXT</edm:type>

  
<dc:type>journal article</dc:type>

  
<dc:type>Wissenschaftlicher Artikel</dc:type>

  
<dc:type>Articolo di rivista</dc:type>

  
<dc:type xml:lang="it">Testo</dc:type>

  
<dc:type xml:lang="it">Articolo di rivista</dc:type>

  
<dc:type xml:lang="en">Text</dc:type>

  
<dc:type xml:lang="en">journal article</dc:type>

  
<dc:type xml:lang="de">Text</dc:type>

  
<dc:type xml:lang="de">Wissenschaftlicher Artikel</dc:type>

  
<dc:subject xml:lang="en">Leukaemia</dc:subject>

  
<dc:subject xml:lang="en">Targeted Therapies</dc:subject>

  
<dc:subject xml:lang="en">Translational Research</dc:subject>

  
<dcterms:issued>2025</dcterms:issued>

  
<dc:date>2025</dc:date>

  
<dc:creator>Annika Dechow</dc:creator>

  
<dc:creator>Sanna Timonen</dc:creator>

  
<dc:creator>Aleksandr Ianevski</dc:creator>

  
<dc:creator>Qu Jiang</dc:creator>

  
<dc:creator>Linus Wahnschaffe</dc:creator>

  
<dc:creator>Yayi Peng</dc:creator>

  
<dc:creator>Dennis Jungherz</dc:creator>

  
<dc:creator>Kerstin Becker</dc:creator>

  
<dc:creator>Heidi Neubauer</dc:creator>

  
<dc:creator>Susann Schoenefeldt</dc:creator>

  
<dc:creator>Elvin D. de Araujo</dc:creator>

  
<dc:creator>P. Gunning</dc:creator>

  
<dc:creator>Roman Fleck</dc:creator>

  
<dc:creator>Alexandra Schrader</dc:creator>

  
<dc:creator>Michael Hallek</dc:creator>

  
<dc:creator>Natali Pflug</dc:creator>

  
<dc:creator>Richard Moriggl</dc:creator>

  
<dc:creator>Tero Aittokallio</dc:creator>

  
<dc:creator>Satu Mustjoki</dc:creator>

  
<dc:creator>Till Braun</dc:creator>

  
<dc:creator>Marco Herling</dc:creator>

  
<dc:publisher>Nature Publishing Group</dc:publisher>

  
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