PLoS ONE · 2010 · 353 citations · 30 references
Life SciencesCell BiologyMolecular BiologyAgingGene ExpressionTranscriptional RegulationBiological AgingCancer BiomarkersCellular AgingMicrorna BiologyMicrorna-mediated RegulationNoncoding Rna In CancerAge-related Cancer BiologyMicrorna BiomarkersMicrorna Expression ProfilingMicrorna In CancerMicrorna ProfilingMicrorna Regulation In CancerPi3 Kinase-akt Signaling
Recent evidence supports a role for microRNAs (miRNAs) in regulating the life span of model organisms. However, little is known about how these small RNAs contribute to human aging. Here, we profiled the expression of over 800 miRNAs in peripheral blood mononuclear cells from young and old individuals by real-time RT-PCR analysis. This genome-wide assessment of miRNA expression revealed that the majority of miRNAs studied decreased in abundance with age. We identified nine miRNAs (miR-103, miR-107, miR-128, miR-130a, miR-155, miR-24, miR-221, miR-496, miR-1538) that were significantly lower in older individuals. Among them, five have been implicated in cancer pathogenesis. Predicted targets of several of these miRNAs, including PI3 kinase (PI3K), c-Kit and H2AX, were found to be elevated with advancing age, supporting a possible role for them in the aging process. Furthermore, we found that decreasing the levels of miR-221 was sufficient to cause a corresponding increase in the expression of the predicted target, PI3K. Taken together, these findings demonstrate that changes in miRNA expression occur with human aging and suggest that miRNAs and their predicted targets have the potential to be diagnostic indicators of age or age-related diseases.
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Life Sciences, Hematology, Oncology +11