MicroRNA sponges: progress and possibilities.
By Margaret S. Ebert, Phillip A. Sharp. RNA: A publication of the RNA Society, 2010
617 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/a482738e4a88affaabc54392d1060c3199abad15
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Yvonne Tay
- P. Pandolfi
- John J. Rossi
- Claudia Cava
- Pavel Morozov
- Thomas Tuschl
- Isabella Castiglioni
- Gloria Bertoli
In Molecular Biology
- P. Pandolfi
- Yvonne Tay
- John J. Rossi
- L. Salmena
- John C. Burnett
- Pavel Morozov
- T. Farazi
- Claudia Cava
Citations in the corpus
- Development of microRNA therapeutics is coming of age (2014, neutral): “A miRNA sponge uses transgenic overexpression of RNA molecules harboring complementary binding sites to a miRNA of interest to block the function of a given miRNA or a miRNA family (Ebert & Sharp, 2010).”
- MicroRNAs: New Biomarkers for Diagnosis, Prognosis, Therapy Prediction and Therapeutic Tools for Breast Cancer (2015, methodology): “In recent years, a method has been described to inhibit miRNA function using synthetic mRNAs containing multiple binding sites for a specific miRNA, called miRNA sponges [232, 233].”
- MicroRNAs in human cancer. (2013, background): “Alternatively, “miRNA sponges” have been exploited to reduce miRNA expression in mammalian cells and mouse models by using RNA transcripts expressed from strong promoters containing miRNA-complementary binding sites (reviewed in [ 199 ] ).”
- A ceRNA hypothesis: the Rosetta stone of a hidden RNA language? (2011, background): “They are often cloned into viral vectors so that they can be expressed at high levels (Ebert and Sharp, 2010).”
- miRNAs in human cancer (2010, neutral): “miRNA-complementary binding sites (reviewed in [181]).”
- RNA-based Therapeutics- Current Progress and Future Prospects (2012, background): “Emerging therapeutic strategies to regulate miRNA activity include antisense-miRNA ONs (antagomirs) and RNA competitive inhibitors or decoys (miRNA sponges) (Ebert and Sharp, 2010).”