Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia

KMT2A rearranged infant acute lymphoblastic leukemia patients have a poor prognosis. Here, the authors use high throughput drug screening on primary infant specimens to identify a clinically active chemotherapy combination.

Bibliographic Details
Main Authors: Jennifer L. Kamens, Stephanie Nance, Cary Koss, Beisi Xu, Anitria Cotton, Jeannie W. Lam, Elizabeth A. R. Garfinkle, Pratima Nallagatla, Amelia M. R. Smith, Sharnise Mitchell, Jing Ma, Duane Currier, William C. Wright, Kanisha Kavdia, Vishwajeeth R. Pagala, Wonil Kim, LaShanale M. Wallace, Ji-Hoon Cho, Yiping Fan, Aman Seth, Nathaniel Twarog, John K. Choi, Esther A. Obeng, Mark E. Hatley, Monika L. Metzger, Hiroto Inaba, Sima Jeha, Jeffrey E. Rubnitz, Junmin Peng, Taosheng Chen, Anang A. Shelat, R. Kiplin Guy, Tanja A. Gruber
Format: Article
Language:English
Published: Nature Portfolio 2023-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-36370-x
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author Jennifer L. Kamens
Stephanie Nance
Cary Koss
Beisi Xu
Anitria Cotton
Jeannie W. Lam
Elizabeth A. R. Garfinkle
Pratima Nallagatla
Amelia M. R. Smith
Sharnise Mitchell
Jing Ma
Duane Currier
William C. Wright
Kanisha Kavdia
Vishwajeeth R. Pagala
Wonil Kim
LaShanale M. Wallace
Ji-Hoon Cho
Yiping Fan
Aman Seth
Nathaniel Twarog
John K. Choi
Esther A. Obeng
Mark E. Hatley
Monika L. Metzger
Hiroto Inaba
Sima Jeha
Jeffrey E. Rubnitz
Junmin Peng
Taosheng Chen
Anang A. Shelat
R. Kiplin Guy
Tanja A. Gruber
author_facet Jennifer L. Kamens
Stephanie Nance
Cary Koss
Beisi Xu
Anitria Cotton
Jeannie W. Lam
Elizabeth A. R. Garfinkle
Pratima Nallagatla
Amelia M. R. Smith
Sharnise Mitchell
Jing Ma
Duane Currier
William C. Wright
Kanisha Kavdia
Vishwajeeth R. Pagala
Wonil Kim
LaShanale M. Wallace
Ji-Hoon Cho
Yiping Fan
Aman Seth
Nathaniel Twarog
John K. Choi
Esther A. Obeng
Mark E. Hatley
Monika L. Metzger
Hiroto Inaba
Sima Jeha
Jeffrey E. Rubnitz
Junmin Peng
Taosheng Chen
Anang A. Shelat
R. Kiplin Guy
Tanja A. Gruber
author_sort Jennifer L. Kamens
collection DOAJ
description KMT2A rearranged infant acute lymphoblastic leukemia patients have a poor prognosis. Here, the authors use high throughput drug screening on primary infant specimens to identify a clinically active chemotherapy combination.
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spelling doaj.art-2cd886b587c94bdaa2bd04fdff8499132023-03-22T11:41:05ZengNature PortfolioNature Communications2041-17232023-02-0114111310.1038/s41467-023-36370-xProteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemiaJennifer L. Kamens0Stephanie Nance1Cary Koss2Beisi Xu3Anitria Cotton4Jeannie W. Lam5Elizabeth A. R. Garfinkle6Pratima Nallagatla7Amelia M. R. Smith8Sharnise Mitchell9Jing Ma10Duane Currier11William C. Wright12Kanisha Kavdia13Vishwajeeth R. Pagala14Wonil Kim15LaShanale M. Wallace16Ji-Hoon Cho17Yiping Fan18Aman Seth19Nathaniel Twarog20John K. Choi21Esther A. Obeng22Mark E. Hatley23Monika L. Metzger24Hiroto Inaba25Sima Jeha26Jeffrey E. Rubnitz27Junmin Peng28Taosheng Chen29Anang A. Shelat30R. Kiplin Guy31Tanja A. Gruber32Department of Pediatrics, Stanford University School of MedicineDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Computational Biology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Pediatrics, Stanford University School of MedicineThe University of Tennessee Health Science CenterDepartment of Pediatrics, Stanford University School of MedicineDepartment of Pediatrics, Stanford University School of MedicineDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Chemical Biology and Therapeutics, St. Jude Children’s Research HospitalDepartment of Chemical Biology and Therapeutics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalDepartment of Computational Biology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Chemical Biology and Therapeutics, St. Jude Children’s Research HospitalDepartment of Pathology, University of Alabama School of MedicineDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalDepartment of Chemical Biology and Therapeutics, St. Jude Children’s Research HospitalDepartment of Chemical Biology and Therapeutics, St. Jude Children’s Research HospitalDepartment of Pharmaceutical Sciences, University of KentuckyDepartment of Pediatrics, Stanford University School of MedicineKMT2A rearranged infant acute lymphoblastic leukemia patients have a poor prognosis. Here, the authors use high throughput drug screening on primary infant specimens to identify a clinically active chemotherapy combination.https://doi.org/10.1038/s41467-023-36370-x
spellingShingle Jennifer L. Kamens
Stephanie Nance
Cary Koss
Beisi Xu
Anitria Cotton
Jeannie W. Lam
Elizabeth A. R. Garfinkle
Pratima Nallagatla
Amelia M. R. Smith
Sharnise Mitchell
Jing Ma
Duane Currier
William C. Wright
Kanisha Kavdia
Vishwajeeth R. Pagala
Wonil Kim
LaShanale M. Wallace
Ji-Hoon Cho
Yiping Fan
Aman Seth
Nathaniel Twarog
John K. Choi
Esther A. Obeng
Mark E. Hatley
Monika L. Metzger
Hiroto Inaba
Sima Jeha
Jeffrey E. Rubnitz
Junmin Peng
Taosheng Chen
Anang A. Shelat
R. Kiplin Guy
Tanja A. Gruber
Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
Nature Communications
title Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
title_full Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
title_fullStr Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
title_full_unstemmed Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
title_short Proteasome inhibition targets the KMT2A transcriptional complex in acute lymphoblastic leukemia
title_sort proteasome inhibition targets the kmt2a transcriptional complex in acute lymphoblastic leukemia
url https://doi.org/10.1038/s41467-023-36370-x
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