[HTML][HTML] Integrated analysis of dysregulated ncRNA and mRNA expression profiles in humans exposed to carbon nanotubes

AA Shvedova, N Yanamala, ER Kisin, TO Khailullin… - PloS one, 2016 - journals.plos.org
AA Shvedova, N Yanamala, ER Kisin, TO Khailullin, ME Birch, LM Fatkhutdinova
PloS one, 2016journals.plos.org
Background As the application of carbon nanotubes (CNT) in consumer products continues
to rise, studies have expanded to determine the associated risks of exposure on human and
environmental health. In particular, several lines of evidence indicate that exposure to multi-
walled carbon nanotubes (MWCNT) could pose a carcinogenic risk similar to asbestos
fibers. However, to date the potential markers of MWCNT exposure are not yet explored in
humans. Methods In the present study, global mRNA and ncRNA expression profiles in the …
Background
As the application of carbon nanotubes (CNT) in consumer products continues to rise, studies have expanded to determine the associated risks of exposure on human and environmental health. In particular, several lines of evidence indicate that exposure to multi-walled carbon nanotubes (MWCNT) could pose a carcinogenic risk similar to asbestos fibers. However, to date the potential markers of MWCNT exposure are not yet explored in humans.
Methods
In the present study, global mRNA and ncRNA expression profiles in the blood of exposed workers, having direct contact with MWCNT aerosol for at least 6 months (n = 8), were compared with expression profiles of non-exposed (n = 7) workers (e.g., professional and/or technical staff) from the same manufacturing facility.
Results
Significant changes in the ncRNA and mRNA expression profiles were observed between exposed and non-exposed worker groups. An integrative analysis of ncRNA-mRNA correlations was performed to identify target genes, functional relationships, and regulatory networks in MWCNT-exposed workers. The coordinated changes in ncRNA and mRNA expression profiles revealed a set of miRNAs and their target genes with roles in cell cycle regulation/progression/control, apoptosis and proliferation. Further, the identified pathways and signaling networks also revealed MWCNT potential to trigger pulmonary and cardiovascular effects as well as carcinogenic outcomes in humans, similar to those previously described in rodents exposed to MWCNTs.
Conclusion
This study is the first to investigate aberrant changes in mRNA and ncRNA expression profiles in the blood of humans exposed to MWCNT. The significant changes in several miRNAs and mRNAs expression as well as their regulatory networks are important for getting molecular insights into the MWCNT-induced toxicity and pathogenesis in humans. Further large-scale prospective studies are necessary to validate the potential applicability of such changes in mRNAs and miRNAs as prognostic markers of MWCNT exposures in humans.
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