GATA1 downregulation in prefibrotic and fibrotic stages of primary myelofibrosis and in the myelofibrotic progression of other myeloproliferative neoplasms.


Journal

Leukemia research
ISSN: 1873-5835
Titre abrégé: Leuk Res
Pays: England
ID NLM: 7706787

Informations de publication

Date de publication:
01 2021
Historique:
received: 04 11 2020
revised: 30 11 2020
accepted: 09 12 2020
pubmed: 29 12 2020
medline: 12 3 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

GATA binding protein 1 (GATA1) is a transcription factor essential for effective erythropoiesis and megakaryopoiesis. Two isoforms of GATA1 exist, derived from alternative splicing. "GATA1" is the full length and functionally active protein; "GATA1s" is the truncated isoform devoid of the activation domain, the function of which has not been fully elucidated. Reduced megakaryocytic expression of GATA1 has been linked to impaired hematopoiesis and bone marrow fibrosis in murine models and in vivo in patients affected by primary myelofibrosis (PMF). However, data is limited regarding GATA1 expression in other myeloproliferative neoplasms (MPN) such as pre-fibrotic PMF (pre-PMF), polycythemia vera (PV) and essential thrombocythemia (ET) and in their respective fibrotic progression. To assess whether an immunohistologic approach can be of help in separating different MPN, we have performed a comprehensive immunohistochemical evaluation of GATA1 expression in megakaryocytes within a cohort of BCR-ABL1 negative MPN. In order to highlight any potential differences between the two isoforms we tested two clones, one staining the sum of GATA1 and GATA1s ("clone 1"), the other staining GATA1 full length alone ("clone 2"). At the chronic phase, a significant reduction preferentially of GATA1 full length was seen in pre-fibrotic PMF, particularly compared to ET and PV; no significant differences were observed between PV and ET. The fibrotic progression of both PV and ET was associated with a significant reduction in GATA1, particularly affecting the GATA1 full length isoform. The fibrotic progression of pre-PMF to PMF was associated with a significant reduction of the overall GATA1 protein and a trend in reduction of GATA1s. Our findings support a role of GATA1 in the pathogenesis of BCR-ABL1 negative MPN, particularly in their fibrotic progression and suggest that the immunohistochemical evaluation of GATA1 may be of use in the differential diagnosis of these neoplasms.

Identifiants

pubmed: 33360878
pii: S0145-2126(20)30200-9
doi: 10.1016/j.leukres.2020.106495
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
GATA1 Transcription Factor 0
GATA1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106495

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Valentina Fabiola Ilenia Sangiorgio (VFI)

Department of Cellular Pathology, the Royal London Hospital, London, UK; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, NY, USA. Electronic address: valentina.sangiorgio@nhs.net.

Anna Nam (A)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, NY, USA. Electronic address: shn9035@med.cornell.edu.

Zhengming Chen (Z)

Department of Population Health Sciences, Weill Cornell Medicine, NY, USA. Electronic address: zhc2006@med.cornell.edu.

Attilio Orazi (A)

Department of Pathology, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA. Electronic address: attilio.orazi@ttuhsc.edu.

Wayne Tam (W)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, NY, USA. Electronic address: wtam@med.cornell.edu.

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Classifications MeSH