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miR-15a targets the HSP90 co-chaperone Morgana in chronic myeloid leukemia.

Pietro Poggio | Stefania Rocca | Federica Fusella | Roberta Ferretti | Ugo Ala | Flora D'Anna | Emilia Giugliano | Cristina Panuzzo | Diletta Fontana | Valeria Palumbo | Giovanna CarrĂ  | Daniela Taverna | Carlo Gambacorti-Passerini | Giuseppe Saglio | Carmen Fava | Rocco Piazza | Alessandro Morotti | Francesca Orso | Mara Brancaccio
Scientific reports | 2024

Morgana is a ubiquitous HSP90 co-chaperone protein coded by the CHORDC1 gene. Morgana heterozygous mice develop with age a myeloid malignancy resembling human atypical myeloid leukemia (aCML), now renamed MDS/MPN with neutrophilia. Patients affected by this pathology exhibit low Morgana levels in the bone marrow (BM), suggesting that Morgana downregulation plays a causative role in the human malignancy. A decrease in Morgana expression levels is also evident in the BM of a subgroup of Philadelphia-positive (Ph+) chronic myeloid leukemia (CML) patients showing resistance or an incomplete response to imatinib. Despite the relevance of these data, the mechanism through which Morgana expression is downregulated in patients' bone marrow remains unclear. In this study, we investigated the possibility that Morgana expression is regulated by miRNAs and we demonstrated that Morgana is under the control of four miRNAs (miR-15a/b and miR-26a/b) and that miR-15a may account for Morgana downregulation in CML patients.

Pubmed ID: 38956394

Associated grants

  • Agency: Ricerca Finalizzata Giovani Ricercatori,
    Id: GR-2021-12374957
  • Agency: Associazione Italiana per la Ricerca sul Cancro,
    Id: IG15880

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

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