Polycomb Factor PHF19 Controls Cell Growth and Differentiation Toward Erythroid Pathway in Chronic Myeloid Leukemia Cells

Other authors

Institut Català de la Salut

[García-Montolio M, Ballaré C, Blanco E, Gutiérrez A, Aranda S] Epigenetics Events in Cancer Laboratory, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology, Barcelona, Spain. [Gómez A] Grup de Recerca en Reumatologia, Servei de Reumatologia, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2021-12-16T12:38:01Z

2021-12-16T12:38:01Z

2021-04-29



Abstract

Leucèmia mieloide crònica; Diferenciació eritroïdal; Polycomb


Leucemia mieloide crónica; Diferenciación eritroide; Polycomb


Chronic myeloid leukemia; Erythroid differentiation; Polycomb


Polycomb group (PcG) of proteins are a group of highly conserved epigenetic regulators involved in many biological functions, such as embryonic development, cell proliferation, and adult stem cell determination. PHD finger protein 19 (PHF19) is an associated factor of Polycomb repressor complex 2 (PRC2), often upregulated in human cancers. In particular, myeloid leukemia cell lines show increased levels of PHF19, yet little is known about its function. Here, we have characterized the role of PHF19 in myeloid leukemia cells. We demonstrated that PHF19 depletion decreases cell proliferation and promotes chronic myeloid leukemia (CML) differentiation. Mechanistically, we have shown how PHF19 regulates the proliferation of CML through a direct regulation of the cell cycle inhibitor p21. Furthermore, we observed that MTF2, a PHF19 homolog, partially compensates for PHF19 depletion in a subset of target genes, instructing specific erythroid differentiation. Taken together, our results show that PHF19 is a key transcriptional regulator for cell fate determination and could be a potential therapeutic target for myeloid leukemia treatment.


This work was supported by the Di Croce Laboratory is supported by grants from the Spanish Ministry of Science and Innovation (BFU2016-75008-P and PID2019-108322GB-100), “Fundación Vencer El Cancer” (VEC), the European Regional Development Fund (FEDER), and from AGAUR (SGR 2017-2019). We acknowledge the support of the Spanish Ministry of Science and Innovation to the EMBL partnership, the Centro de Excelencia Severo Ochoa and the CERCA Programme/Generalitat de Catalunya. PV was supported by the Fundación Científica de la Asociación Española Contra el Cáncer. SA was funded by the Ramon y Cajal program of the Ministerio de Ciencia, Innovación y Universidades, the European Social Fund under the reference number RYC-2018-025002-I, and the Instituto de Salud Carlos III-FEDER (PI19/01814).

Document Type

Article


Published version

Language

English

Publisher

Frontiers Media

Related items

Frontiers in Cell and Developmental Biology;9

https://doi.org/10.3389/fcell.2021.655201

info:eu-repo/grantAgreement/ES/PE2013-2016/BFU2016-75008-P

info:eu-repo/grantAgreement/ES/PE2017-2020/PID2019-108322GB-100

info:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F01814

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Rights

Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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