Abstract Recently it was reported that microRNA from the miR-17 ~ 92 family may have a key role in chronic lymphocytic leukemia (CLL). Here, we designed specific oligonucleotides to target endogenous miR-17 (antagomiR17). In-vitro administration of antagomiR17 effectively reduced miR-17 expression and the proliferation of CLL-like MEC-1 cells. When injected in-vivo in tumor generated by the MEC-1 cells in SCID mice, antagomiR17 dramatically reduced tumor growth and significantly increase survival. Altogether, our results provide the rationale for the use of antagomiR17 as a novel potential therapeutic tool in CLL and in other lymphoproliferative disorders where miR-17 has a driver role in tumor progression.

Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia / Dereani, Sara; Macor, Paolo; D'Agaro, Tiziana; Mezzaroba, Nelly; Dal Bo, Michele; Capolla, Sara; Zucchetto, Antonella; Tissino, Erika; Poeta, Giovanni Del; Zorzet, Sonia; Gattei, Valter; Bomben, Riccardo. - In: JOURNAL OF HEMATOLOGY & ONCOLOGY. - ISSN 1756-8722. - ELETTRONICO. - 7:79(2014), pp. "-"-"-". [10.1186/s13045-014-0079-z]

Potential therapeutic role of antagomiR17 for the treatment of chronic lymphocytic leukemia.

DEREANI, SARA;MACOR, PAOLO;D'AGARO, TIZIANA;MEZZAROBA, NELLY;CAPOLLA, SARA;ZUCCHETTO, ANTONELLA;ZORZET, SONIA;BOMBEN, RICCARDO
2014-01-01

Abstract

Abstract Recently it was reported that microRNA from the miR-17 ~ 92 family may have a key role in chronic lymphocytic leukemia (CLL). Here, we designed specific oligonucleotides to target endogenous miR-17 (antagomiR17). In-vitro administration of antagomiR17 effectively reduced miR-17 expression and the proliferation of CLL-like MEC-1 cells. When injected in-vivo in tumor generated by the MEC-1 cells in SCID mice, antagomiR17 dramatically reduced tumor growth and significantly increase survival. Altogether, our results provide the rationale for the use of antagomiR17 as a novel potential therapeutic tool in CLL and in other lymphoproliferative disorders where miR-17 has a driver role in tumor progression.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2859924
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