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Updated: May 16, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Very early effect of DMBA and MNU on microRNA expression
Krisztina Juhász1, Katalin Gombos, Mónika Szirmai
1Institute of Public Health, Faculty of Medicine, University of Pécs, Pécs, 12 Szigeti str., 7624 Hungary. krisztina.juhasz01@gmail.com
Background:
microRNA expression profile analysis provides evaluation of the early stages of carcinogenesis. This study focuses on early alteration of miRNA expression after treatment with different carcinogens.
Materials And Methods:
Mice were intraperitoneally injected with one dose of 7,12-dimethylbenz(α)anthracene (DMBA) and N-methyl-N-nitrosourea (MNU). The expression of miRNAs were analyzed 3 and 6 hours after the treatment, using quantitative real-time-polymerase chain reaction.
Results:
Underexpression of miR-34a and miR-155 were detected in the liver, spleen and kidneys at 3 and 6 hours after MNU treatment. In the lungs and kidneys, the expression of miR-21 was significantly elevated 6 hours after DMBA treatment, while in the liver, MNU induced higher expression levels of miR-21 at 3 and 6 hours compared to treatment with DMBA.
Conclusion:
The different response of miRNAs to carcinogens emphasizes their possible role as potential epidemiological biomarkers in early phases of environmental tumorigenesis.
Insights
Early changes in microRNA (miRNA) expression were observed in mice exposed to carcinogens. These findings highlight miRNAs as potential biomarkers for detecting environmental carcinogenesis in its initial stages.
Area of Science:
- Environmental toxicology
- Molecular biology
- Cancer research
Background:
- MicroRNA (miRNA) expression profiling aids in evaluating early carcinogenesis.
- This study investigates early miRNA expression alterations following exposure to distinct carcinogens.
Purpose of the Study:
- To analyze the impact of specific carcinogens on miRNA expression patterns.
- To identify potential miRNA biomarkers for early environmental tumorigenesis.
Main Methods:
- Mice received single intraperitoneal injections of 7,12-dimethylbenz(α)anthracene (DMBA) or N-methyl-N-nitrosourea (MNU).
- miRNA expression was quantified using quantitative real-time-polymerase chain reaction (qRT-PCR) at 3 and 6 hours post-treatment.
Main Results:
- MNU treatment led to underexpression of miR-34a and miR-155 in the liver, spleen, and kidneys.
- DMBA treatment elevated miR-21 expression in lungs and kidneys 6 hours post-exposure.
- MNU induced higher miR-21 expression in the liver at 3 and 6 hours compared to DMBA.
Conclusions:
- Distinct miRNA responses to different carcinogens were observed.
- These findings support the role of miRNAs as potential epidemiological biomarkers for early environmental carcinogenesis.
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