In IDH1/2 mutated gliomas, the high concentration of D-2-HG could suppress the function of KDM4A, KDM4B, and KDM4C (also known as JmjC-KDM2A, JmjC-KDM2B, and JmjC-KDM2C), and increase histone methylation levels, such as H3K9me3, H3K9me2, H3K36me3, and H3K4me3 [71,72,73]. This evidence concerns the gene KDM4A and glioma.