AI Article Synopsis

  • The article discusses the significance of spliceosome mutations in myeloid malignancies, particularly myeloproliferative neoplasms (MPN), highlighting the need for further research on splicing anomalies in this area.
  • It reviews existing clinical data on spliceosome mutations linked to MPN and explores the molecular mechanisms by which these mutations contribute to the disease's development and progression.
  • The authors suggest that abnormal splicing might play a crucial role in the progression of MPN and propose that targeting splicing anomalies could lead to new treatment strategies.

Article Abstract

Since the discovery of spliceosome mutations in myeloid malignancies, abnormal pre-mRNA splicing, which has been well studied in various cancers, has attracted novel interest in hematology. However, despite the common occurrence of spliceosome mutations in myelo-proliferative neoplasms (MPN), not much is known regarding the characterization and mechanisms of splicing anomalies in MPN. In this article, we review the current scientific literature regarding "splicing and myeloproliferative neoplasms". We first analyse the clinical series reporting spliceosome mutations in MPN and their clinical correlates. We then present the current knowledge about molecular mechanisms by which these mutations participate in the pathogenesis of MPN or other myeloid malignancies. Beside spliceosome mutations, splicing anomalies have been described in myeloproliferative neoplasms, as well as in acute myeloid leukemias, a dreadful complication of these chronic diseases. Based on splicing anomalies reported in chronic myelogenous leukemia as well as in acute leukemia, and the mechanisms presiding splicing deregulation, we propose that abnormal splicing plays a major role in the evolution of myeloproliferative neoplasms and may be the target of specific therapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464941PMC
http://dx.doi.org/10.3390/cancers12082216DOI Listing

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