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, S., Macor, P., D'Agaro, T., Mezzaroba, N., Dal Bo, M., Capolla, S., Zucchetto, A., Tissino, E., Poeta, G.D., Zorzet, S., Gattei, V., Bomben, R.. - 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.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


