Abstract | BACKGROUND: METHODS: RESULTS: Four serum miRNAs, that is miR-126, miR-205, miR-222, and miR-520g, were found to be implicated in asbestos-related malignant diseases. Notably, increased expression of miR-126 and miR-222 were found in asbestos-exposed subjects, and both miRNAs are involved in major pathways linked to cancer development. Epigenetic changes and cancer-stroma cross-talk could induce repression of miR-126 to facilitate tumor formation, angiogenesis, and invasion. CONCLUSIONS: This study indicates that miRNAs are potentially involved in asbestos-related malignancies, and their expression outlines mechanism(s) whereby miRNAs may be involved in an asbestos-induced pathogenesis. IMPACT: The discovery of a miRNA panel for asbestos-related malignancies would impact on occupational compensation and may be utilized for screening asbestos-exposed populations.
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Authors | Lory Santarelli, Simona Gaetani, Federica Monaco, Massimo Bracci, Matteo Valentino, Monica Amati, Corrado Rubini, Armando Sabbatini, Ernesto Pasquini, Nunzia Zanotta, Manola Comar, Jiri Neuzil, Marco Tomasetti, Massimo Bovenzi |
Journal | Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
(Cancer Epidemiol Biomarkers Prev)
Vol. 28
Issue 1
Pg. 119-126
(01 2019)
ISSN: 1538-7755 [Electronic] United States |
PMID | 30257964
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | ©2018 American Association for Cancer Research. |
Chemical References |
- Biomarkers, Tumor
- Carcinogens
- MIRN126 microRNA, human
- MIRN205 microRNA, human
- MIRN222 microRNA, human
- MicroRNAs
- Asbestos
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Topics |
- Aged
- Asbestos
(toxicity)
- Biomarkers, Tumor
(blood)
- Carcinogens
(toxicity)
- Carcinoma, Non-Small-Cell Lung
(chemically induced)
- Female
- Gene Expression Regulation, Neoplastic
- Humans
- Lung Neoplasms
(chemically induced)
- Male
- Mesothelioma
(chemically induced)
- Mesothelioma, Malignant
- MicroRNAs
(blood, genetics)
- Middle Aged
- Sensitivity and Specificity
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