Small Molecule Inhibition of Micro-RNA-210 Reprograms an Oncogenic Hypoxic Circuit
Herein, we describe the identification of a small molecule named Targapremir-210 that binds to the Dicer site of the miR-210 hairpin precursor. This interaction inhibits production of the mature miRNA, de-represses glycerol-3-phosphate dehydrogenase 1-like enzyme (GPD1 L), a hypoxia-associated protein negatively regulated by miR-210, decreases HIF-1 a, and triggers apoptosis of triple negative breast cancer cells only under hypoxic conditions. Further, Targapremir-210 inhibits tumorigenesis in a mouse xenograft model of hypoxic triple negative breast cancer. We applied Chemical Cross-Linking and Isolation by Pull Down (Chem-CLIP) to study the cellular selectivity and the on- and off-targets of Targapremir-210. Targapremir-210 selectively recognizes the miR-210 precursor and can differentially recognize RNAs in cells that have the same target motif but have different expression levels, revealing this important feature for selectively drugging RNAs for the first time.
1 . A method of inhibiting biogenesis of microRNA miR-210 in a cell under hypoxic conditions, comprising contacting the cell with an effective amount or concentration of a compound of formula
2 . The method of claim 1 , wherein the Targapremir-210 selectively recognizes the miR-210 precursor and can differentially recognize RNAs in cells that have the same target motif but have different expression levels.
3 . A method of target profiling a set of cells for expression of a miR-210 microRNA precursor, comprising administering an effective amount or concentration of Targapermir-210 to the set of cells, then screening the set of cells for expression or suppression of a phenotype associated with miR-210.
4 . A method of impeding tumor proliferation in a mammal in vivo, comprising administering to the animal an effective dose of a compound of of formula
5 . The method of claim 4 , wherein the tumor is breast cancer.