Open Biology (May 2020)

EZN-2208 treatment suppresses chronic lymphocytic leukaemia by interfering with environmental protection and increases response to fludarabine

  • Roberta Valsecchi,
  • Nadia Coltella,
  • Daniela Magliulo,
  • Lucia Bongiovanni,
  • Lydia Scarfò,
  • Paolo Ghia,
  • Maurilio Ponzoni,
  • Rosa Bernardi

DOI
https://doi.org/10.1098/rsob.190262
Journal volume & issue
Vol. 10, no. 5

Abstract

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The transcription factor HIF-1α is overexpressed in chronic lymphocytic leukaemia (CLL), where it promotes leukaemia progression by favouring the interaction of leukaemic cells with protective tissue microenvironments. Here, we tested the hypothesis that a pharmacological compound previously shown to inhibit HIF-1α may act as a chemosensitizer by interrupting protective microenvironmental interactions and exposing CLL cells to fludarabine-induced cytotoxicity. We found that the camptothecin-11 analogue EZN-2208 sensitizes CLL cells to fludarabine-induced apoptosis in cytoprotective in vitro cultures; in vivo EZN-2208 improves fludarabine responses, especially in early phases of leukaemia expansion, and exerts significant anti-leukaemia activity, thus suggesting that this or similar compounds may be considered as effective CLL therapeutic approaches.

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