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. 2023 Jun 9;12(12):1595. doi: 10.3390/cells12121595

Table 2.

Summary of described histone modifications.

Source Modification Modifying Agent Proposed Downstream Mechanism Resulting Cellular Changes
[33] H2A monoubiquitination ALKBH5 Increased USP22 and RNF 40 expression Increased cell viability, cell proliferation, and migration
[35] Decreased H3K27me3 KDM6B LDHA overexpression Increased metastasis
[36] Decreased H3K27me3 KDM6A/KDM6B PRCKA overexpression Cisplatin resistance and decreased apoptosis
[39] Decreased H4K20 me3 decreased SUV420H2 expression Multiple signaling pathways Not studied
[40] Modified H3K36me3 SETD2 Not studied
[42] Increased H3T3ph Sirt1 Increased ATG 5/13/14 expression Increased autophagy
[45] Decreased HDAC2 and DNAMT3a Treatment with VPA and 5-Aza Increased stem cell factors (OCT4, NANOG, SOX2, and CD133) Increased stem cell phenotype, cell proliferation, and migration
[47] Decreased H3K9me2 and increased PTEN methylation G9a and DNMT3B Suppressed PTEN signaling Malignant BM-MSC transformation