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The levels of miR-452, DROSHA mRNA, and DICER mRNA of SW872 cells treated with normoxia or IH for 24 h. The levels of miR-452 and DROSHA and DICER mRNAs were measured by real-time RT-PCR using U6 (for miR-452) and β-actin (for DROSH and DICER) as an endogenous control. Data are expressed as mean ± SE for each group (n = 4–6). The statistical analyses were performed using Student’s t-test.
