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Hyde, R. Katherine

https://orcid.org/0000-0003-2808-1749

Mayo Clinic

University of Nebraska Medical Center

Citations 1

Cooperative role of distinctive TP53 and PTEN combined loss in the peripheral T cell lymphoma–GATA3 molecular subgroup
Lone, Waseem , Yu, Jiayu , Liu, Xuxiang , Jochum, Dylan T. , Bouska, Alyssa , Shetty, Kunal , Herek, Tyler A. , Sharma, Sunandini , Bi, Chengfeng , Shah, Ab Rauf , Nasser, Zaina W., Amador, Catalina , Arif, Aiza, Mir, Abdul Rouf , Li, Yuping , Heavican‐Foral, Tayla B. , Robinson, Jacob E. , Hyde, R. Katherine , Sakata‐Yanagimoto, Mamiko , Rachagani, Satyanarayana , McKeithan, Timothy W. , Scott, David W. , Staudt, Louis M. , Feldman, Andrew L. , Greiner, Timothy C. , Vose, Julie M. , Khoury, Joseph D. , Chan, Wing C. , Iqbal, Javeed , Lone, Waseem G , Shah, Rauf , Feldman, Andrew L , Greiner, Timothy C , Vose, Julie , Rimsza, Lisa, Khoury, Joseph , Chan, Wing C , Iqbal, Javeed , Scott, David W , Bouska, Alyssa , Amador, Catalina , Jochum, Dylan , Heavican, Tayla B., Robinson, Jacob, Inghirami, Giorgio , Rimsza, Lisa M.

Science Advances | October 17, 2025 | Volume: 11 | Issue: 42 | Pages: No page available

10.1126/sciadv.adx6877 Get It

Peripheral T cell lymphoma (PTCL) is a heterogeneous group of postthymic T cell neoplasms, with ~40% classified as PTCL–not otherwise specified (PTCL-NOS). PTCL-GATA3, a molecularly defined subtype, associated with T helper 2 (T H 2)–like differentiation and poor prognosis, has frequent co-occurrence of TP53 loss/mutation and heterozygous PTEN loss. CD4+ T cell conditional mouse models with Trp53 mutation/deletion and Pten loss demonstrated mature T cell lymphomas (mTCLs) with T H 2-like transcriptomic and immunophenotypic profiles. Molecular studies revealed that codeletion of Trp53/Pten induced T cell receptor and Janus kinase–signal transducer and activator of transcription signaling, promoting T H 2 differentiation while inhibiting T H 1 differentiation. These findings were validated by CRISPR editing of TP53/PTEN loss in human CD4+ T cells and mechanistically evaluated the p53 binding region in intron-3 of GATA3, resulting in transcriptional repression. Transcriptomic profiles of m-TCLs recapitulated human-PTCL-GATA3 transcriptome and distinguished PTCL-NOS subtypes. Preclinical assessment of m-TCLs with PI3Kγ/δ inhibitors significantly improved survival, supporting a therapeutic approach for the p53-aberrant PTCL-GATA3.