期刊论文详细信息
International Journal of Molecular Sciences
Small Nucleolar RNAs Determine Resistance to Doxorubicin in Human Osteosarcoma
Giulio Ferrero1  Francesca Cordero1  Federica Di Nicolantonio2  Chiara Riganti2  Martina Godel2  Ilaria Buondonno2  Riccardo Taulli2  Preeta Ananthanarayanan2  Deborah Morena2  Joanna Kopecka2  Massimo Serra3  ClaudiaM. Hattinger3 
[1] Department of Computer Science, University of Torino, 10149 Torino, Italy;Department of Oncology, University of Torino, 1026 Torino, Italy;Laboratory of Experimental Oncology, Pharmacogenomics and Pharmacogenetics Research Unit, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy;
关键词: osteosarcoma;    doxorubicin;    chemoresistance;    small nucleolar RNAs;   
DOI  :  10.3390/ijms21124500
来源: DOAJ
【 摘 要 】

Doxorubicin (Dox) is one of the most important first-line drugs used in osteosarcoma therapy. Multiple and not fully clarified mechanisms, however, determine resistance to Dox. With the aim of identifying new markers associated with Dox-resistance, we found a global up-regulation of small nucleolar RNAs (snoRNAs) in human Dox-resistant osteosarcoma cells. We investigated if and how snoRNAs are linked to resistance. After RT-PCR validation of snoRNAs up-regulated in osteosarcoma cells with different degrees of resistance to Dox, we overexpressed them in Dox-sensitive cells. We then evaluated Dox cytotoxicity and changes in genes relevant for osteosarcoma pathogenesis by PCR arrays. SNORD3A, SNORA13 and SNORA28 reduced Dox-cytotoxicity when over-expressed in Dox-sensitive cells. In these cells, GADD45A and MYC were up-regulated, TOP2A was down-regulated. The same profile was detected in cells with acquired resistance to Dox. GADD45A/MYC-silencing and TOP2A-over-expression counteracted the resistance to Dox induced by snoRNAs. We reported for the first time that snoRNAs induce resistance to Dox in human osteosarcoma, by modulating the expression of genes involved in DNA damaging sensing, DNA repair, ribosome biogenesis, and proliferation. Targeting snoRNAs or down-stream genes may open new treatment perspectives in chemoresistant osteosarcomas.

【 授权许可】

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