Table 2.
miRNA regulation of particulate matter and nanoparticle toxicity response.
| Xenobiotic | Time of exposure | miRNAs | Health endpoints | References |
|---|---|---|---|---|
| 100 μg/ml PM2.5 | 6−120 hpf | let-7b | Up regulation - Regulates genes in DNA repair and breast cancer | [28] |
| miR-153 | Up regulation - Associated with hypertension in rats | |||
| miR-122 | Up regulation - Regulates hypoxia based glucose metabolism | |||
| miR-24 | Up regulation - Roles in immunity and inflammation | |||
| let-7i let-7i | Down regulation - Role in immunity | |||
| miR-7a/b | Down regulation - Cardiomyocyte protective | |||
| miR-19b-3p | Down regulation - Inhibits cardiac fibrogenesis | |||
| 3 mg/mL Silica nanoparticle, 0.01 mg/ml MeHg | 48 hpf | miR-7147, miR-26a | Down regulation | [29] |
| miR-26amiR-375, miR-206 | Up regulation(Many miRNAs and genes assessed but the authors focused on these miRNAs that were part of a pathway for cardiac muscle contraction) | |||
| In silico nanoparticles | miR-124 | Key regulator for Wnt signaling and implicated in DNA double strand damage | [20] | |
| miR-144 | Key mediator for oxidative stress | |||
| miR-19a | Important in oncogene regulation and in inflammatory responses | |||
| miR-155a | Inflammatory response mediator with MAPK and TNF signaling as candidate pathways | |||
| miR-223 | Predicted in three networks as a key regulator in tissue damage |