Table 3.
Dietary phytochemicals and histone modification.
Dietary Agent | Molecular mechanism(s) | Target genes | In vitro model | In vivo model | Disease Type | Dose/Concentration | Ref. |
---|---|---|---|---|---|---|---|
| |||||||
Apigenin | HDAC inhibitor | p21 | PC-3 cells | Mouse xenograft | Prostate cancer | 20–50 μM (20–50 μg/day) | 86 |
HDAC inhibitor | NA | Skin cancer cells (mouse) | 1.56–50 μM | 87 | |||
| |||||||
Curcumin | HAT & HDAC inhibitor | H3/H4 deacetylation GATA4, EOMES, GZMB, PRF1 |
Cervix, HIV, Hepatoma Leukemia, Prostate Brain, Lymphoma |
Plasmodium falciparum; Herpes Virus Mouse: Rat |
Malaria Herpes Epilepsy Diabetes and Heart failure |
0.3–75mg/kg (6.25–135μM) |
96–106 214–222 |
| |||||||
Catechin | HAT inhibitor | NA | Lymphocytes | NA | 100 μM | 223 | |
Epicatechin | HAT inhibitor | NA | Lymphocytes | NA | 100 μM | 223 | |
Epicatechin-gallate | HAT inhibitor | NA | Lymphocytes, Colon | NA | 100 μM | 223 | |
| |||||||
Epigalocatechin-3-gallate | HAT inhibitor | H3/H4 acetylation | Lymphocytes, Colon | NA | Cancer | 5–100 μM | 223 |
HMT inhibitor | H3K27 trimethylation NF-κB, IL-6, BMI-1, EZH2, SUZ12 |
Keratinocytes, Prostate | NA | ||||
| |||||||
Equol | HDAC inhibitor | H2A/H2B/H3/H4 | Drosophila | NA | 12.8 μM | 130 | |
Genistein | HAT inhibitor | Acetylation H2A/H2B/H3/H4 |
Esophageal; Prostate, Breast, Renal | NA | Cancer | 5–100 μM | 124, 127, 128, 130, 131, |
HADC inhibitor | Acetylation p21, p16, PTEN, p53 FOXA3, SIRT1, hTERT |
NA | |||||
| |||||||
Daidzein | HDAC inhibitor | Histone acetylation | Esophageal, Prostate | NA | Cancer | 12.8–100 μM | 130, 210 |
| |||||||
Indole-3 carbinol Diindolylmethane | HDAC inhibitor | IFN-γ, TNF-α, IL-6, IL-2, NF-κB, COX-2, iNOS, IL-1β, IL-12 | Prostate cancer | Sprague-Dawley rats | 20–80 μg/rat | 82, 141, 143–150 | |
Colon Cancer | Nude mice | Cancer | 15–100 μM | ||||
Spleenocytes (CD3+ cells) | Nude mice | 15–100 μM 100–300 mg/kg 100 μM 40 mg/kg |
|||||
| |||||||
Allicin | unknown | H4 acetylation | Erythroleukemia | NA | 2–200 μM | 157–159 | |
Allyl mercaptan | SIRT1 inhibitor | H3/H4 acetylation P21/WAF1 |
Erythroleukemia Liver, Colon |
Rat: liver | Cancer | 2–500 μM (100mg/kg) | 157–159, 224 |
S-allymercapto-Cysteine | HAT inhibitor | H3/H4 acetylation | Erythroleukemia | NA | 20–250 μM | 156, 161 | |
Diallyl disulphide | HDAC inhibitor | H3/H4 acetylation P21/WAF1 |
Erythroleukemia, Leukemia, Liver, Colon, Prostate, Fibroblast | Rat | Cancer | 20–200 μM (42–200 mg/kg) |
156–159,161 224 |
| |||||||
Quercetin | SIRTI activator | IP-10, MIP-2 | Cervix, Drosophila Small intestine |
Cancer Mouse |
Inflammatory diseases | 100 μM | 164–175, |
HAT inhibitor | Bowel inflammation | 181,182 | |||||
| |||||||
Resveratrol | SIRTi activator | TNF-α, IL-8, RBP | Cervix, Endothelial Embryonic kidney, Macrophages, Lungs, Liver, Cardiomyocytes | Yeast, Drosophila Mouse Rats |
Colon cancer Lung cancer |
10–200 μM | 177–191 |
| |||||||
Sulforaphane | HDAC inhibitor | H3/H4 acetylation RARβ, HBD-2, p21, Bax |
Prostate, Breast, Colon, Kidney | Mouse, prostate cancer xenografts | Cancer | 15–25 μM (443 μg/kg, 68g) | 193–203, 225–227 |
NA, information not available