4.4 Article

Upregulated hypoxia inducible factor 1α signaling pathway in high risk myelodysplastic syndrome and acute myeloid leukemia patients is associated with better response to 5-azacytidine-data from the Hellenic myelodysplastic syndrome study group

Journal

HEMATOLOGICAL ONCOLOGY
Volume 39, Issue 2, Pages 231-242

Publisher

WILEY
DOI: 10.1002/hon.2834

Keywords

hypoxia inducible factor 1 alpha (Hif‐ 1α ) signaling pathway; immunohistochemistry (IHC); myelodysplastic syndrome (MDS); quantitative real‐ time PCR; treatment response; 5‐ azacytidine (5‐ Α Ζ Α )

Funding

  1. Celgene [GRANT-GRC-084]

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The study suggests a possible association between the Hif-1α signaling pathway and response to 5-AZA therapy in MDS/AML patients, with high Hif-1α mRNA expression correlated with better survival rates and identified as an independent predictor of response to 5-AZA therapy. The data also offer new perspectives on MDS combinational therapies, proposing a potential synergistic activity of 5-AZA and Hif-1α inducers like PHDi.
5-azacytidine (5-AZA) is considered the standard of care for patients with high-risk myelodysplastic syndromes (MDS) and patients with acute myeloid leukemia (AML) not candidate for intensive chemotherapy. However, even after an initial favorable response, almost all patients relapse, with the exact mechanisms underlying primary or secondary 5-AZA resistance remaining largely unknown. Several reports have previously demonstrated the significance of hypoxia in the regulation of both physiological and malignant hematopoiesis. In MDS, high hypoxia inducible factor 1 alpha (Hif-1 alpha) expression has been correlated with poor overall survival and disease progression, while its involvement in the disease's pathogenesis was recently reported. We herein investigated the possible association of the Hif-1 alpha signaling pathway with response to 5-AZA therapy in MDS/AML patients. Our data demonstrated that 5-AZA-responders present with higher Hif-1 alpha mRNA and protein expression compared to 5-AZA-non-responders/stable disease patients, before the initiation of therapy, while, interestingly, no significant differences in Hif-1 alpha mRNA expression at the 6-month follow-up were observed. Moreover, we found that 5-AZA-responders exhibited elevated mRNA levels of the Hif-1 alpha downstream targets lactate dehydrogenase a (LDHa) and BCL2 interacting protein 3 like (BNIP3L), a further indication of an overactivated Hif-1a signaling pathway in these patients. Kaplan-Meier survival analysis revealed a significant correlation between high Hif-1 alpha mRNA expression and better survival rates, while logistic regression analysis showed that Hif-1 alpha mRNA expression is an independent predictor of response to 5-AZA therapy. From the clinical point of view, apart from proposing Hif-1 alpha mRNA expression as a significant predictive factor for response to 5-AZA, our data offer new perspectives on MDS combinational therapies, suggesting a potential synergistic activity of 5-AZA and Hif-1 alpha inducers, such as propyl hydroxylases inhibitors (PHDi).

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