Table 4.
Interaction between miRNAs and asbestos.
miRNA | Human/animal Study | Dose | Cell line | Dose | Targets | Observations | Ref |
---|---|---|---|---|---|---|---|
hsa-let-7a, miR-125a-5p, miR-320, miR-484, (Up) | Human (Malignant pleural mesothelioma patients) | – | – | – | WNT3, FGF9, TGFB2 | The expression of miRNAs could be changed in pleural effusion induced by asbestos. | [90] |
miR-30d (Down) | Human (pleural malignant mesothelioma patients) | – | NCI–H2452 | Vimentin, CDH1, TWIST1 | Exposure of NCI–H2452 cells to asbestos could suppress invasion or migration via miR-30d. | [91] | |
miR-30e-3p, miR-103a-3p, (Down) | Human (malignant pleural mesothelioma patients) | – | – | – | – | Extracellular vesicle miRNAs could be considered a biomarker of mentioned disease. | [92] |
hsa-miR-98 (Down) | Human (Malignant pleural mesothelioma patients), GSE92636 database | – | – | – | – | Higher expression of miR-98 was associated with poor overall survival in patients with mesothelioma. | [93] |
miR-126, miR-222, (Up) | Human (samples from malignant mesothelioma patients) | – | HUVECs, BEAS-2B, IMR-90, Met-5A | 5 μg/cm2 | EGFR, AKT, ERK, p38, PARP1 | Exposed cells to asbestos via activating the EGFR pathway could increase the expression of mentioned miRs | [94] |
miR-126 (Up), miR-520g (−), miR-222 (Up), miR-205 (−) | Human (non–small cell lung cancer patients) | – | – | – | – | Mentioned-miRNAs could be changed in lung malignancies caused by asbestos. | [20] |
miR-197-3p (dysregulated) | Human | – | – | – | Serum levels of miR-197-3p could be dysregulated in workers exposed to asbestos. | [95] | |
miRNA profile, miR-197-3p, miR-1281, (Up) | Human (malignant pleural mesothelioma patients) | – | – | – | – | In workers who are ex-exposed to asbestos, the level of mentioned miRNAs increased. | [96] |
miR-199/214 (Up) | specific pathogen-free F1 hybrid rats | – | MeT5A | – | Twist1, Akt, ERK, PTEN | In an animal model of sarcomatoid mesothelioma induced by asbestos, higher expression of miR-199/214 via targeting Twist1 could increase tumorigenesis. | [97] |