Presence of CD34 + in Megakaryocytes in Association With p53 Expression Predicts Unfavorable Prognosis in Low-risk Myelodysplastic Syndrome Patients.

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  • Additional Information
    • Source:
      Publisher: International Institute of Anticancer Research Country of Publication: Greece NLM ID: 8806809 Publication Model: Print Cited Medium: Internet ISSN: 1791-7549 (Electronic) Linking ISSN: 0258851X NLM ISO Abbreviation: In Vivo Subsets: MEDLINE
    • Publication Information:
      Publication: <2000- > : Attiki, Greece : International Institute of Anticancer Research
      Original Publication: Athens : Dr. J.G. Delinassios
    • Subject Terms:
    • Abstract:
      Background/aim: Although risk stratification using the Prognostic Scores Systems (IPSS, WPSS and IPSS-R) incorporate key information about prognosis of patients with Myelodysplastic syndromes (MDS), patients classified as low-risk may evolve rapidly and aggressively, despite a "favorable" prognostic stratification. The aim of this study was to identify biomarkers for predicting prognosis, and for better stratification and management of these patients.
      Materials and Methods: Expression of CD34 and p53 in megakaryocytes was examined by immunohistochemistry in 71 MDS patients classified as low-risk.
      Results: CD34 staining in megakaryocytes was associated with p53 expression (p=0.0166). CD34 and p53 expression were associated to worse overall survival in patients (p=0.0281).
      Conclusion: The presence of CD34 in megakaryocytes is associated with p53 expression and an adverse prognosis for MDS patients.
      (Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
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    • Contributed Indexing:
      Keywords: CD34 on megakaryocytes; Myelodysplastic syndromes; low risk; p53 protein expression; prognosis
    • Accession Number:
      0 (Antigens, CD34)
      0 (TP53 protein, human)
      0 (Tumor Suppressor Protein p53)
    • Publication Date:
      Date Created: 20181228 Date Completed: 20190404 Latest Revision: 20200225
    • Publication Date:
      20240628
    • Accession Number:
      PMC6364072
    • Accession Number:
      10.21873/invivo.11472
    • Accession Number:
      30587636