MicroRNAs (miRNAs) are one of the most prevalent small (~22 nucleotide) regulatory RNA classes in
animals. These miRNAs constitute nearly one percent of genes in the human genome, making miRNA genes
one of the more abundant types of regulatory molecules. MiRNAs have been shown to play important roles
in cell development, apoptosis, and other fundamental biological processes. MiRNAs exert their influence
through complementary base-pairing with specific target mRNAs, leading to degradation or translational
repression of the targeted mRNA. We have identified and tested a novel microRNA (miR-491) and
demonstrated increased apoptosis in hepatocellular carcinoma cells (HepG2) and in human breast cancer
cells (HBT3477) in vitro. We prepared a novel cancer targeting assembly of gold nanoparticles (GNP) with
Quantum dots, miR-491, and MAb-ChL6 coupled through streptavidin/biotin for effective transfection, and
to induce apoptosis in specific cancer cells for imaging and targeted therapy. The targeting and apoptosis
inducing ability was tested by confocal and electron microscopy. The MAb-GNP-miR491-Qdot construct
effectively transfected into the HBT3477 cells and induced apoptosis the confirmation of these results would
suggest a new class of molecules for the imaging and therapy of breast cancer.
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