Cited by 648Acute Myeloid Leukemia ResearchCancer-related Molecular PathwaysRetinoids in leukemia and cellular processes

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Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Open access
Bernard, Elsa, Nannya, Yasuhito, Hasserjian, Robert P., Devlin, Sean M., Tuechler, Heinz, Medina-Martinez, Juan S., Yoshizato, Tetsuichi, Shiozawa, Yusuke, Saiki, Ryunosuke, Malcovati, Luca, Levine, Max F., Arango, Juan E., Zhou, Yangyu, Solé, Francesc, Cargo, Catherine A., Haase, Detlef, Creignou, Maria, Germing, Ulrich, Zhang, Yanming, Gundem, Gunes, Sarian, Araxe, van de Loosdrecht, Arjan A., Jädersten, Martin, Tobiasson, Magnus, Kosmider, Olivier, Follo, Matilde Y., Thol, Felicitas, Pinheiro, Ronald F., Santini, Valeria, Kotsianidis, Ioannis, Boultwood, Jacqueline, Santos, Fabio P. S., Schanz, Julie, Kasahara, Senji, Ishikawa, Takayuki, Tsurumi, Hisashi, Takaori-Kondo, Akifumi, Kiguchi, Toru, Polprasert, Chantana, Bennett, John M., Klimek, Virginia M., Savona, Michael R., Belickova, Monika, Ganster, Christina, Palomo, Laura, Sanz, Guillermo, Ades, Lionel, Della Porta, Matteo Giovanni, Elias, Harold K., Smith, Alexandra G., Werner, Yesenia, Patel, Minal, Viale, Agnès, Vanness, Katelynd, Neuberg, Donna S., Stevenson, Kristen E., Menghrajani, Kamal, Bolton, Kelly L., Fenaux, Pierre, Pellagatti, Andrea, Platzbecker, Uwe, Heuser, Michael, Valent, Peter, Chiba, Shigeru, Miyazaki, Yasushi, Finelli, Carlo, Voso, Maria Teresa, Shih, Lee-Yung, Fontenay, Michaela, Jansen, Joop H., Cervera, José, Atsuta, Yoshiko, Gattermann, Norbert, Ebert, Benjamin L., Bejar, Rafael, Greenberg, Peter L., Cazzola, Mario, Hellström-Lindberg, Eva, Ogawa, Seishi, Papaemmanuil, Elli·2020·Nature Medicine

Published version of a preprint

Abstract

Tumor protein p53 (TP53) is the most frequently mutated gene in cancer 1,2. In patients with myelodysplastic syndromes (MDS), TP53 mutations are associated with high-risk disease 3,4, rapid transformation to acute myeloid leukemia (AML)5, resistance to conventional therapies 6-8 and dismal outcomes 9. Consistent with the tumor-suppressive role of TP53, patients harbor both mono- and biallelic mutations 10. However, the biological and clinical implications of TP53 allelic state have not been fully investigated in MDS or any other cancer type. We analyzed 3,324 patients with MDS for TP53 mutations and allelic imbalances and delineated two subsets of patients with distinct phenotypes and outcomes. One-third of TP53-mutated patients had monoallelic mutations whereas two-thirds had multiple hits (multi-hit) consistent with biallelic targeting. Established associations with complex karyotype, few co-occurring mutations, high-risk presentation and poor outcomes were specific to multi-hit patients only. TP53 multi-hit state predicted risk of death and leukemic transformation independently of the Revised International Prognostic Scoring System (IPSS-R)11. Surprisingly, monoallelic patients did not differ from TP53 wild-type patients in outcomes and response to therapy. This study shows that consideration of TP53 allelic state is critical for diagnostic and prognostic precision in MDS as well as in future correlative studies of treatment response.

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Authors
Bernard, E., Nannya, Y., Hasserjian, R. P., Devlin, S. M., Tuechler, H., Medina-Martinez, J. S., Yoshizato, T., Shiozawa, Y., Saiki, R., Malcovati, L., Levine, M. F., Arango, J. E., Zhou, Y., Solé, F., Cargo, C. A., Haase, D., Creignou, M., Germing, U., Zhang, Y., Gundem, G., Sarian, A., van de Loosdrecht, A. A., Jädersten, M., Tobiasson, M., Kosmider, O., Follo, M. Y., Thol, F., Pinheiro, R. F., Santini, V., Kotsianidis, I., Boultwood, J., Santos, F. P. S., Schanz, J., Kasahara, S., Ishikawa, T., Tsurumi, H., Takaori-Kondo, A., Kiguchi, T., Polprasert, C., Bennett, J. M., Klimek, V. M., Savona, M. R., Belickova, M., Ganster, C., Palomo, L., Sanz, G., Ades, L., Della Porta, M. G., Elias, H. K., Smith, A. G., Werner, Y., Patel, M., Viale, A., Vanness, K., Neuberg, D. S., Stevenson, K. E., Menghrajani, K., Bolton, K. L., Fenaux, P., Pellagatti, A., Platzbecker, U., Heuser, M., Valent, P., Chiba, S., Miyazaki, Y., Finelli, C., Voso, M. T., Shih, L.-Y., Fontenay, M., Jansen, J. H., Cervera, J., Atsuta, Y., Gattermann, N., Ebert, B. L., Bejar, R., Greenberg, P. L., Cazzola, M., Hellström-Lindberg, E., Ogawa, S., & Papaemmanuil, E.
Affiliations
  • Memorial Sloan Kettering Cancer Center (US)
  • Kyoto University (JP)
  • Massachusetts General Hospital (US)
  • University of Pavia (IT)
  • Josep Carreras Leukaemia Research Institute (ES)
  • St James's University Hospital (GB)
  • Universitätsmedizin Göttingen (DE)
  • Karolinska University Hospital (SE)
  • Heinrich Heine University Düsseldorf (DE)
  • Université Paris Cité (FR)
  • University of Bologna (IT)
  • Medizinische Hochschule Hannover (DE)
  • Universidade Federal do Ceará (BR)
  • Azienda Ospedaliero-Universitaria Careggi (IT)
  • University of Oxford (GB)
  • Gifu Municipal Hospital (JP)
  • Kobe City Medical Center General Hospital (JP)
  • Gifu University (JP)
  • Chugoku Central Hospital (JP)
  • Chulalongkorn University (TH)
  • University of Rochester Medicine (US)
  • Vanderbilt University (US)
  • Instituto de Salud Carlos III (ES)
  • University of York (GB)
  • Dana-Farber Cancer Institute (US)
  • Hôpital Saint-Louis (FR)
  • Leipzig University (DE)
  • Ludwig Boltzmann Institute for Hematology and Oncology (AT)
  • University of Tsukuba (JP)
  • Nagasaki University (JP)
  • IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola (IT)
  • University of Rome Tor Vergata (IT)
  • Chang Gung University (TW)
  • Radboud University Medical Center (NL)
  • Hospital Universitari i Politècnic La Fe (ES)
  • The Japanese Data Center for Hematopoietic Cell Transplantation (JP)
  • Howard Hughes Medical Institute (US)
  • Moores Cancer Center (US)
  • Stanford Cancer Institute (US)
Corresponding author
Papaemmanuil, Elli
Venue
Nature Medicine
Published
2020-08-03
Volume
26
Issue
10
Pages
1549-1556
ISSN
  • 1078-8956 (ISSN-L)
  • 1546-170X
OpenAlex
W3046671820
Cited by
648
References
58
Citations by year
2026: 73 · 2025: 91 · 2024: 106 · 2023: 136 · 2022: 130 · 2021: 87 · 2020: 22
FWCI
59.16
Type
journal article
Language
en
Open access
Locations
  • Nature Medicine (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • Pure Amsterdam UMC (publishedVersion, other-oa)
  • Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
  • White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Florence Research (University of Florence) (submittedVersion, other-oa)
  • Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
  • Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion, other-oa)
  • eScholarship (California Digital Library) (submittedVersion)
  • GoeScholar The Publication Server of the Georg-August-Universität Göttingen (Georg-August-Universität Göttingen) (submittedVersion, cc-by)
  • Radboud Repository (Radboud University) (submittedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
Funders
  • Howard Hughes Medical Institute
  • Amgen
  • Pfizer
  • Sanofi
  • Alexion Pharmaceuticals
  • Celgene (21267)
  • Helsinn
  • European Hematology Association
  • Japan Agency for Medical Research and Development (JP18ck0106353, 19ck0106250h0003, JP19cm0106501)
  • Taiho Pharmaceutical
  • TG Therapeutics
  • Astex Pharmaceuticals
  • Sunesis
  • Incyte
  • Nippon Shinyaku
  • Celltrion
  • Geoffrey Beene Foundation
  • Cancer Research UK (29685)
  • Agence Nationale de la Recherche (ANR-18-IBHU-0003)
  • Ministry of Education, Culture, Sports, Science and Technology (hp160219)
  • Austrian Science Fund (#F4704-B20)
  • Ministero dell’Istruzione, dell’Università e della Ricerca (21267)
  • Astellas Pharma
  • Associazione Italiana per la Ricerca sul Cancro (21267, 5×1000, 20125, 13042, project #21267, IG #20125)
  • Genesis Pharma
  • Otsuka Pharmaceutical
  • Ono Pharmaceutical
  • Blood Cancer UK (13042)
  • Chugai Pharmaceutical
  • Pharmacyclics
  • Sanofi K.K.
  • Japan Society for the Promotion of Science (19H03684, 13042, 18H02836, 26221308, hp160219, 19H05656, 15H05909)
  • National Cancer Institute (P30CA008748, K12CA184746, P50CA254838)
  • Daiichi Sankyo Europe
  • Cilag
Topics
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
Keywords
TP53 mutation, myelodysplastic syndrome, allelic state, monoallelic variants, biallelic variants, genome stability, leukemic transformation, acute myeloid leukemia, complex karyotype, prognosis, treatment response, wild-type p53
MeSH terms
Alleles, DNA Mutational Analysis, Female, Gene Frequency, Humans, Male, Mutation, Myelodysplastic Syndromes, Phenotype, Prognosis, Cohort Studies, Survival Analysis, Tumor Suppressor Protein p53, Treatment Outcome, Loss of Heterozygosity, Genomic Instability, DNA Copy Number Variations

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