: Richter's Transformation (RT) is a poorly understood and fatal progression of chronic lymphocytic leukemia (CLL) manifesting histologically as diffuse large B-cell lymphoma. Protein arginine methyltransferase 5 (PRMT5) is implicated in lymphomagenesis, but its role in CLL or RT progression is unknown. We demonstrate herein that tumors uniformly overexpress PRMT5 in patients with progression to RT. Furthermore, mice with B-specific overexpression of hPRMT5 develop a B-lymphoid expansion with increased risk of death, and Eµ-PRMT5/TCL1 double transgenic mice develop a highly aggressive disease with transformation that histologically resembles RT; where large-scale transcriptional profiling identifies oncogenic pathways mediating PRMT5-driven disease progression. Lastly, we report the development of a SAM-competitive PRMT5 inhibitor, PRT382, with exclusive selectivity and optimal in vitro and in vivo activity compared to available PRMT5 inhibitors. Taken together, the discovery that PRMT5 drives oncogenic pathways promoting RT provides a compelling rationale for clinical investigation of PRMT5 inhibitors such as PRT382 in aggressive CLL/RT cases.

Dysregulation of PRMT5 in chronic lymphocytic leukemia promotes progression with high risk of Richter's transformation / Hing, Zachary A; Walker, Janek S; Whipp, Ethan C; Brinton, Lindsey; Cannon, Matthew; Zhang, Pu; Sher, Steven; Cempre, Casey B; Brown, Fiona; Smith, Porsha L; Agostinelli, Claudio; Pileri, Stefano A; Skinner, Jordan N; Williams, Katie; Phillips, Hannah; Shaffer, Jami; Beaver, Larry P; Pan, Alexander; Shin, Kyle; Gregory, Charles T; Ozer, Gulcin H; Yilmaz, Selen A; Harrington, Bonnie K; Lehman, Amy M; Yu, Lianbo; Coppola, Vincenzo; Yan, Pearlly; Scherle, Peggy; Wang, Min; Pitis, Philip; Xu, Chaoyi; Vaddi, Kris; Chen-Kiang, Selina; Woyach, Jennifer; Blachly, James S; Alinari, Lapo; Yang, Yiping; Byrd, John C; Baiocchi, Robert A; Blaser, Bradley W; Lapalombella, Rosa. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - ELETTRONICO. - 14:1(2023), pp. 97.1-97.21. [10.1038/s41467-022-35778-1]

Dysregulation of PRMT5 in chronic lymphocytic leukemia promotes progression with high risk of Richter's transformation

Agostinelli, Claudio;
2023

Abstract

: Richter's Transformation (RT) is a poorly understood and fatal progression of chronic lymphocytic leukemia (CLL) manifesting histologically as diffuse large B-cell lymphoma. Protein arginine methyltransferase 5 (PRMT5) is implicated in lymphomagenesis, but its role in CLL or RT progression is unknown. We demonstrate herein that tumors uniformly overexpress PRMT5 in patients with progression to RT. Furthermore, mice with B-specific overexpression of hPRMT5 develop a B-lymphoid expansion with increased risk of death, and Eµ-PRMT5/TCL1 double transgenic mice develop a highly aggressive disease with transformation that histologically resembles RT; where large-scale transcriptional profiling identifies oncogenic pathways mediating PRMT5-driven disease progression. Lastly, we report the development of a SAM-competitive PRMT5 inhibitor, PRT382, with exclusive selectivity and optimal in vitro and in vivo activity compared to available PRMT5 inhibitors. Taken together, the discovery that PRMT5 drives oncogenic pathways promoting RT provides a compelling rationale for clinical investigation of PRMT5 inhibitors such as PRT382 in aggressive CLL/RT cases.
2023
Dysregulation of PRMT5 in chronic lymphocytic leukemia promotes progression with high risk of Richter's transformation / Hing, Zachary A; Walker, Janek S; Whipp, Ethan C; Brinton, Lindsey; Cannon, Matthew; Zhang, Pu; Sher, Steven; Cempre, Casey B; Brown, Fiona; Smith, Porsha L; Agostinelli, Claudio; Pileri, Stefano A; Skinner, Jordan N; Williams, Katie; Phillips, Hannah; Shaffer, Jami; Beaver, Larry P; Pan, Alexander; Shin, Kyle; Gregory, Charles T; Ozer, Gulcin H; Yilmaz, Selen A; Harrington, Bonnie K; Lehman, Amy M; Yu, Lianbo; Coppola, Vincenzo; Yan, Pearlly; Scherle, Peggy; Wang, Min; Pitis, Philip; Xu, Chaoyi; Vaddi, Kris; Chen-Kiang, Selina; Woyach, Jennifer; Blachly, James S; Alinari, Lapo; Yang, Yiping; Byrd, John C; Baiocchi, Robert A; Blaser, Bradley W; Lapalombella, Rosa. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - ELETTRONICO. - 14:1(2023), pp. 97.1-97.21. [10.1038/s41467-022-35778-1]
Hing, Zachary A; Walker, Janek S; Whipp, Ethan C; Brinton, Lindsey; Cannon, Matthew; Zhang, Pu; Sher, Steven; Cempre, Casey B; Brown, Fiona; Smith, Porsha L; Agostinelli, Claudio; Pileri, Stefano A; Skinner, Jordan N; Williams, Katie; Phillips, Hannah; Shaffer, Jami; Beaver, Larry P; Pan, Alexander; Shin, Kyle; Gregory, Charles T; Ozer, Gulcin H; Yilmaz, Selen A; Harrington, Bonnie K; Lehman, Amy M; Yu, Lianbo; Coppola, Vincenzo; Yan, Pearlly; Scherle, Peggy; Wang, Min; Pitis, Philip; Xu, Chaoyi; Vaddi, Kris; Chen-Kiang, Selina; Woyach, Jennifer; Blachly, James S; Alinari, Lapo; Yang, Yiping; Byrd, John C; Baiocchi, Robert A; Blaser, Bradley W; Lapalombella, Rosa
File in questo prodotto:
File Dimensione Formato  
s41467-022-35778-1.pdf

accesso aperto

Tipo: Versione (PDF) editoriale
Licenza: Licenza per Accesso Aperto. Altra tipologia di licenza compatibile con Open Access
Dimensione 20.65 MB
Formato Adobe PDF
20.65 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/918987
Citazioni
  • ???jsp.display-item.citation.pmc??? 6
  • Scopus 10
  • ???jsp.display-item.citation.isi??? 6
social impact