Correlation Engine 2.0
Clear Search sequence regions


  • adult (1)
  • BCL2L11 (1)
  • blood (1)
  • centenarians (7)
  • cognitive (1)
  • donors (2)
  • female (1)
  • FoxO (1)
  • gene (1)
  • humans (2)
  • micrornas (6)
  • miR 19a (4)
  • mirn19 microrna, human (1)
  • mirn19 microrna, human (1)
  • phase (2)
  • plasma (1)
  • PTEN (1)
  • rna (1)
  • SMAD4 (1)
  • therapies (1)
  • Sizes of these terms reflect their relevance to your search.

    Blood circulating microRNAs (c-miRs) are potential biomarkers to trace aging and longevity trajectories to identify molecular targets for anti-aging therapies. Based on a cross-sectional study, a discovery phase was performed on 12 donors divided into four groups: young, old, healthy, and unhealthy centenarians. The identification of healthy and unhealthy phenotype was based on cognitive performance and capabilities to perform daily activities. Small RNA sequencing identified 79 differentially expressed c-miRs when comparing young, old, healthy centenarians, and unhealthy centenarians. Two miRs, that is, miR-19a-3p and miR-19b-3p, were found increased at old age but decreased at extreme age, as confirmed by RT-qPCR in 49 donors of validation phase. The significant decrease of those miR levels in healthy compared to unhealthy centenarians appears to be due to the presence of isomiRs, not detectable with RT-qPCR, but only with a high-resolution technique such as deep sequencing. Bioinformatically, three main common targets of miR-19a/b-3p were identified, that is, SMAD4, PTEN, and BCL2L11, converging into the FoxO signaling pathway, known to have a significant role in aging mechanisms. For the first time, this study shows the age-related increase of plasma miR-19a/b-3p in old subjects but a decrease in centenarians. This decrease is more pronounced in healthy centenarians and was confirmed by the modified pattern of isomiRs comparing healthy and unhealthy centenarians. Thus, our study paves the way for functional studies using c-miRs and isomiRs as additional parameter to track the onset of aging and age-related diseases using new potential biomarkers. © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

    Citation

    Cristina Morsiani, Lucia Terlecki-Zaniewicz, Susanna Skalicky, Maria Giulia Bacalini, Salvatore Collura, Maria Conte, Federica Sevini, Paolo Garagnani, Stefano Salvioli, Matthias Hackl, Johannes Grillari, Claudio Franceschi, Miriam Capri. Circulating miR-19a-3p and miR-19b-3p characterize the human aging process and their isomiRs associate with healthy status at extreme ages. Aging cell. 2021 Jul;20(7):e13409

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 34160893

    View Full Text