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. 2019 May 4;26(4):2023–2033. doi: 10.1007/s12253-019-00663-8

Table 2.

Histone acetylation/methylation/phosphory marks in CRC

Modification and sites Method Impaired function References
Histone acetylation marks
  Global H3ac CHIP, WB Hyperacetylation (CRC tissues) [39]
  Global H4ac IHC Hypoacetylayion (CRC cell lines) induced by CPERT [40]
  H3K9ac IHC Hypoacetylation (CRC liver metastasis) [41]
  H3K18ac IHC Hypoactylation (CRC cell lines) [42]
  H3K27ac MS,WB Hyperacetylation (CRC tissues) [43]
  H3K56ac

WB, CHIP

RT-qPCR

Hypoacetylation (CRC cell lines) through RAS-PI3K signal pathway. [44]
  H4K12ac IHC Hypoacetylation (CRC cell lines) [42]
  H4K16ac

LC-ES/MS

IHC

Hypoacetylation (CRC cell lines, CRC primary tumors) [45, 46]
Histone methylation marks
  H3K4me2 CHIP, WB Hypermethylation (CRC tissues) [39]
  H3K4me3 IHC Hypomethylation (CRC tissues) [46]
  H3K9me2 IHC, WB Hypermethylation (CRC cells line, CRC liver metastasis) [41, 47]
  H3K27me2 IHC Hypermethylation (CRC tissues) [48]
  H3K27me3 IHC Hypermethylation (CRC tissues) [49]
  H3K36me2 IHC Hypomethylation (CRC liver metastasis) [48]
  H3K79me2 IHC Hypermethylation (Patient with CRC) [50]
  H4K20me2 LC-ES/MS Hypomethylation (CRC cell lines) [45]
  H4K20me3 CHIP, PCR Hypomethylation (CRC patient’s plasma) [51]
Histone phosphorylation marks
  H3S10ph IHC Hypophosphorylation (CRC cell lines) [52]
  H2AX IHC Hyperphosphorylation (CRC patients) [53]