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Deepening Our Understanding of the Factors Affecting Landscape of Myeloproliferative Neoplasms: What Do We Know about Them?

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dc.contributor.author Morales, María-Luz
dc.contributor.author Ferrer-Marín, Francisca
dc.date.accessioned 2025-11-24T12:35:20Z
dc.date.available 2025-11-24T12:35:20Z
dc.date.issued 2023-02
dc.identifier.citation Morales ML, Ferrer-Marín F. Deepening Our Understanding of the Factors Affecting Landscape of Myeloproliferative Neoplasms: What Do We Know about Them? Cancers. 20 de febrero de 2023;15(4):1348.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/22238
dc.description.abstract Myeloproliferative neoplasms (MPNs) arise from the uncontrolled proliferation of hematopoietic stem and progenitor cells in bone marrow. As with all tumors, the development of MPNs is a consequence of alterations in malignant cells and their interaction with other extrinsic factors that support and promote tumor progression. Since the discovery of driver mutations, much work has focused on studying and reviewing the genomic features of the disease but has neglected to delve into the important role that many other mechanisms may play. This review discusses the genetic component of MPNs but focuses mainly on some of the most relevant work investigating other non-genetic factors that may be crucial for the disease. The studies summarized here address MPN cell-intrinsic or -extrinsic factors and the interaction between them through transcriptomic, proteomic and microbiota studies, among others.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/es/ *
dc.title Deepening Our Understanding of the Factors Affecting Landscape of Myeloproliferative Neoplasms: What Do We Know about Them?
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 36831689
dc.relation.publisherversion https://www.mdpi.com/2072-6694/15/4/1348
dc.identifier.doi 10.3390/cancers15041348
dc.journal.title Cancers
dc.identifier.essn 2072-6694


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