Abstract | BACKGROUND:
Neuroblastoma is a paediatric cancer which originates from precursor cells of the sympathetic nervous system. Previous studies have shown that miR-184 expression has anti-proliferative effects in neuroblastoma cells grown in culture. Therefore, it was of interest to evaluate this effect in vivo. MATERIALS AND METHODS:
Neuroblastoma cells overexpressing miR-184 were injected retroperitoneally into CB17-SCID mice and tumour burden was assessed by measuring bioluminescence. Overall survival was also evaluated. RESULTS: Ectopic overexpression of miR-184 in neuroblastoma cell lines is anti-proliferative. In addition, overexpression of miR-184 led to a significant reduction in tumour growth relative to negative control-treated cohorts in a xenograft model of neuroblastoma. CONCLUSION: This study demonstrated for the first time that miR-184 significantly reduces tumour growth and increases overall survival in an orthotopic murine model of neuroblastoma through assessment of tumour growth and moribundity relative to control miRNA-treated cohorts.
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Authors | Amanda Tivnan, Niamh H Foley, Lorraine Tracey, Andrew M Davidoff, Raymond L Stallings |
Journal | Anticancer research
(Anticancer Res)
Vol. 30
Issue 11
Pg. 4391-5
(Nov 2010)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 21115884
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- MIRN184 microRNA, mouse
- MicroRNAs
- RNA, Messenger
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Topics |
- Animals
- Cell Proliferation
- Disease Models, Animal
- Gene Expression Regulation, Neoplastic
(physiology)
- Humans
- Mice
- Mice, SCID
- MicroRNAs
(genetics)
- Neuroblastoma
(genetics, pathology)
- RNA, Messenger
(genetics)
- Reverse Transcriptase Polymerase Chain Reaction
- Survival Rate
- Tumor Cells, Cultured
- Xenograft Model Antitumor Assays
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