H4C1, H4 clustered histone 1, 8359

N. diseases: 121; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.320 GeneticVariation disease BEFREE A novel histone H4 variant H4G regulates rDNA transcription in breast cancer. 31219579 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.320 Biomarker disease BEFREE In total, we identify and quantify 233 proteoforms of histone H4 in two breast cancer cell lines. 29667342 2018
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.320 GeneticVariation disease UNIPROT
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 Biomarker group BEFREE This approach is validated on different types of samples, including formalin-fixed paraffin-embedded pathology tissues, and employed to profile histone H4 modifications in cancer samples and normal tissues, identifying previously reported differences, as well as novel ones. 30471193 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 PosttranslationalModification group BEFREE In the lungs, acrylamide exposure resulted in a decrease of histone H4 lysine 20 trimethylation (H4K20me3), a common epigenetic feature of human cancer, while in the livers, there was increased acetylation of histone H3 lysine 27 (H3K27ac), a gene transcription activating mark. 30807115 2019
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 PosttranslationalModification group BEFREE In the lungs, acrylamide exposure resulted in a decrease of histone H4 lysine 20 trimethylation (H4K20me3), a common epigenetic feature of human cancer, while in the livers, there was increased acetylation of histone H3 lysine 27 (H3K27ac), a gene transcription activating mark. 30807115 2019
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 Biomarker group BEFREE This approach is validated on different types of samples, including formalin-fixed paraffin-embedded pathology tissues, and employed to profile histone H4 modifications in cancer samples and normal tissues, identifying previously reported differences, as well as novel ones. 30471193 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 Biomarker group BEFREE Abbreviations: ALS: Amyotrophic Lateral Sclerosis; APP: Amyloid Precursor Protein gene; CASP3: Caspase 3 gene; CASP9: Caspase 9 gene; H2AFX: H2A histone family, member X gene; HIST1H2AL: Histone H2A type 1 gene; HIST1H2BK: Histone H2B type 1-K gene; HIST1H3J: Histone H3J gene; HIST1H4B: Histone H4B gene; HIST2H2BE: Histone H2B type 2-E gene; HUGO: human genome organization; KM: Kaplan-Meier survival curve; MAPT: Tau gene; OV: Ovarian cancer; SNCA: alpha-syneculin gene; TARDBP: Transactive response DNA binding protein 43 kDa; TCGA: the cancer genome atlas. 30394813 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 GeneticVariation group BEFREE Methylation of histone H4 lysine 20 (H4K20) has been associated with cancer. 29616094 2018
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 GeneticVariation group BEFREE Methylation of histone H4 lysine 20 (H4K20) has been associated with cancer. 29616094 2018
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 Biomarker group BEFREE Abbreviations: ALS: Amyotrophic Lateral Sclerosis; APP: Amyloid Precursor Protein gene; CASP3: Caspase 3 gene; CASP9: Caspase 9 gene; H2AFX: H2A histone family, member X gene; HIST1H2AL: Histone H2A type 1 gene; HIST1H2BK: Histone H2B type 1-K gene; HIST1H3J: Histone H3J gene; HIST1H4B: Histone H4B gene; HIST2H2BE: Histone H2B type 2-E gene; HUGO: human genome organization; KM: Kaplan-Meier survival curve; MAPT: Tau gene; OV: Ovarian cancer; SNCA: alpha-syneculin gene; TARDBP: Transactive response DNA binding protein 43 kDa; TCGA: the cancer genome atlas. 30394813 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 AlteredExpression group BEFREE In normal RWPE-1 cells and even stronger in cancer DU145 cells, the combined treatment induced both AR gene expression on the mRNA level and increased histone H4 acetylation in AR gene promoter. 27499010 2016
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 AlteredExpression group BEFREE In normal RWPE-1 cells and even stronger in cancer DU145 cells, the combined treatment induced both AR gene expression on the mRNA level and increased histone H4 acetylation in AR gene promoter. 27499010 2016
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 PosttranslationalModification group BEFREE The genome-wide loss of histone H4 lysine 20 tri-methylation (H4K20me3) is observed in multiple types of cancer, including breast tumors. 25814362 2015
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 PosttranslationalModification group BEFREE The genome-wide loss of histone H4 lysine 20 tri-methylation (H4K20me3) is observed in multiple types of cancer, including breast tumors. 25814362 2015
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 GeneticVariation group BEFREE Alterations in histone H4 lysine 20 methylation: implications for cancer detection and prevention. 22035019 2012
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 GeneticVariation group BEFREE Alterations in histone H4 lysine 20 methylation: implications for cancer detection and prevention. 22035019 2012
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 Biomarker group BEFREE Global profiling of histone changes in some human cancers demonstrated that loss of histone H4 acetylation at lysine16 (H4KA16) and trimethylation at lysine 20 (H4KM20) was a common hallmark of cancer. 21415707 2011
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 Biomarker group BEFREE Global profiling of histone changes in some human cancers demonstrated that loss of histone H4 acetylation at lysine16 (H4KA16) and trimethylation at lysine 20 (H4KM20) was a common hallmark of cancer. 21415707 2011
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 Biomarker group BEFREE Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. 15765097 2005
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 Biomarker group BEFREE Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. 15765097 2005
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.070 Biomarker group BEFREE Beside H4K20me3, plasma histone H4 is a useful marker to discriminate colonic tumors from precancerous polyps and other conditions. 31471419 2020
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.070 AlteredExpression group BEFREE Glioma-induced SIRT1-dependent activation of hMOF histone H4 lysine 16 acetyltransferase in microglia promotes a tumor supporting phenotype. 29308302 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.070 Biomarker group BEFREE Further, we demonstrate that the observed hypo-acetylation of histone H4 in tissue and serum samples of tumor bearing animals corroborated with the elevated HDAC activity in both samples compared to normal. 28360947 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.070 AlteredExpression group BEFREE Whereas the levels of H4 and histone acetyltransferases were stable irrespective of HRD status, the levels of histone H4 acetylation and one HDAC, HDAC6, were elevated in the HRD tumors. 28866885 2017