The sequence‐based RNA adenosine methylation site predictor (SRAMP) online tool was used to predict m6A modifications in IGFBP7. Based on the predicted m6A primer pairs, we designed corresponding primers for meRIP‐PCR/qPCR. A Magna MeRIP m6A Kit (cat. no. 17–10,499, Millipore Sigma, MA, USA) was used to verify m6A modification in GC cells following the manufacturer's instructions. In brief, anti‐m6A antibody‐coated magnetic beads were coimmunoprecipitated with 150 μg of fragmented mRNA according to the protocols of the GenSeqTM m6A‐MeRIP Kit (GenSeq, Beijing, China). The eluent was used for m6A RNA elution and purification. PCR and reverse transcription (RT)‐qPCR assays were then performed on the abundance of eluted RNA samples with gene‐specific primers to analyse the mRNA levels of m6A sites.
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