Increased expression of miR-34a in mouse spleen one day after exposure to N-ethyl-N-nitrosourea
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Updated: May 25, 2026

Measuring DNA Damage and Repair in Mouse Splenocytes After Chronic In Vivo Exposure to Very Low Doses of Beta- and Gamma-Radiation
Published on: July 3, 2015
David Chen1, Zhiguang Li, Tao Chen
1Little Rock Central High School, Little Rock, AR 72206, USA.
Abstract:
MicroRNAs (miRNAs) are a class of single-stranded small RNA molecules (~22 nucleotides) that are not translated into proteins and function as regulators of gene expression. Many miRNAs are involved in carcinogenesis. One of them, miR-34a, is associated with various p53-initiated biological processes and may act as a tumor suppressor miRNA. Its expression is generally down-regulated in tumor tissues and up-regulated in tissues exposed to carcinogens chronically or subchronically. However, the response of this miRNA to acute exposure of a genotoxic carcinogen is little known. In this study, miR-34a expression was evaluated in spleen tissues of mice treated with a dose of 120 mg kg(-1) body weight N-ethyl-N-nitrosourea (ENU), a potent mutagenic carcinogen. Real-time PCR analysis showed that the ENU exposure resulted in a 5.5-fold increase of miR-34a expression over the control one day after the treatment. The result suggests that miR-34a expression responds sensitively to genotoxic insults within a short period after exposure of the mutagen, and therefore, this gene has the potential to be used as an indicator for genotoxin exposure.