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A decade of exploring the cancer epigenome—biological and translational implications
Open accessAbstract
The past decade has highlighted the central role of epigenetic processes in cancer causation, progression and treatment. Next-generation sequencing is providing a window for visualizing the human epigenome and how it is altered in cancer. This view provides many surprises, including linking epigenetic abnormalities to mutations in genes that control DNA methylation, the packaging and the function of DNA in chromatin, and metabolism. Epigenetic alterations are leading candidates for the development of specific markers for cancer detection, diagnosis and prognosis. The enzymatic processes that control the epigenome present new opportunities for deriving therapeutic strategies designed to reverse transcriptional abnormalities that are inherent to the cancer epigenome.
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“Conversely, disruption of chromosomal topology and oncogene insulation may be more generally relevant to methylator phenotypes observed in colorectal and renal cell carcinomas, leukemia and other malignancies28.”
From Insulator dysfunction and oncogene activation in IDH mutant gliomas (2016) · cites this paper as [28]
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“Previous studies showed that enhanced histone acetylation induced by HDACi allowed the overexpression of genes involved in cell cycle arrest such as cyclin-dependent kinase inhibitors or the growth arrest and DNA damage-inducible protein GADD45 gene family (11, 28, 40, 45-49).”
From Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability (2013) · cites this paper as [11]
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“Insulator dysfunction may also be accompanied by promoter silencing events28,29, and by alterations to other pathways affected by 2-HG7,30.”
From Insulator dysfunction and oncogene activation in IDH mutant gliomas (2016) · cites this paper as [28]
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“Among them, novel selective benzamide-based HDAC1/2 inhibitors have been described that exhibit greater than 100-fold selectivity relative to other HDACs (11, 28).”
From Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability (2013) · cites this paper as [11]
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“It has previously been shown that HDAC inhibitors such as SAHA and MS-275 promote cell cycle arrest and apoptosis”
From Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability (2013) · cites this paper as [11]
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“Among activated genes that subside with pulsed HDACi administration are genes known to be powerful effectors of cell cycle arrest in multiple cell types and may promote apoptosis (11, 50).”
From Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability (2013) · cites this paper as [11]
Experimental — accuracy not yet measuredIn the citing paper
“Three general processes have major effects on cancer initiation and progression. First, discrete somatic mutations lead to tumor suppressor loss-of-function and oncoprotein gain-of-function [1]; second, epigenetic alterations change patterns of gene expression [2]; and third, alterations in the tumor microenvironment also lead to broad changes in gene expression [3].”
From The hypoxic tumor microenvironment: A driving force for breast cancer progression (2016) · cites this paper as [2]
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Cites
Coussens, L. M., & Werb, Z. (2002) · Nature · doi:10.1038/nature01322 · Cited by 15,111
Chromatin modifications and their function
Kouzarides, T. (2007) · Cell · doi:10.1016/j.cell.2007.02.005 · Cited by 10,883
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
The Cancer Genome Atlas Research Network (2008) · Nature · doi:10.1038/nature07385 · Cited by 7,735
MGMT Gene Silencing and Benefit from Temozolomide in Glioblastoma
Hegi, M. E., Diserens, A.-C., Gorlia, T., Hamou, M.-F., de Tribolet, N., Weller, M., Kros, J. M., Hainfellner, J. A., Mason, W., Mariani, L., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa043331 · Cited by 7,405
DNA methylation patterns and epigenetic memory
Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124
IDH1 and IDH2 Mutations in Gliomas
Yan, H., Parsons, D. W., Jin, G., McLendon, R., Rasheed, B. A., Yuan, W., Kos, I., Batinic-Haberle, I., Jones, S., Riggins, G. J., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0808710 · Cited by 5,847
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836
The fundamental role of epigenetic events in cancer
Jones, P. A., & Baylin, S. B. (2002) · Nature Reviews Genetics · doi:10.1038/nrg816 · Cited by 5,648
Self-citationA bivalent chromatin structure marks key developmental genes in embryonic stem cells
Bernstein, B. E., Mikkelsen, T. S., Xie, X., Kamal, M., Huebert, D. J., Cuff, J., Fry, B., Meissner, A., Wernig, M., Plath, K., et al. (2006) · Cell · doi:10.1016/j.cell.2006.02.041 · Cited by 5,361
Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis
Gupta, R. A., Shah, N., Wang, K., Kim, J., Horlings, H. M., Wong, D. J., Tsai, M.-C., Hung, T., Argani, P., Rinn, J. L., et al. (2010) · Nature · doi:10.1038/nature08975 · Cited by 5,205
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Research works printed but not linked: 3
- Allis, C., Jenuwein, T. & Reinberg, D. Epigenetics (ed. Caparros, M.) (Cold Spring Harbor Laboratory Press, 2007).
- Allis, C. D., Jenuwein, T, Reinberg, D. Overview and concepts (Cold Spring Harbor Laboratory Press, New York, 2007).
- Gilbert, M. R. et al. in ASCO Annual Meeting 2011 Abstr. 2006. (University of Texas M. D. Anderson Cancer Center, Chicago, 2011).
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Sorted by citations
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López, V., Fernández, A. F., & Fraga, M. F. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.05.002 · Cited by 101
Matsushima-Miyagi, T., Hatano, K., Nomura, M., Liu, L., Nishikawa, T., Saga, K., Shimbo, T., & Kaneda, Y. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-12-1595 · Cited by 96
Li, Z., Dai, H., Martos, S. N., Xu, B., Gao, Y., Teng, L., Zhu, G., Schones, D. E., & Wang, Z. (2015) · Genome biology · doi:10.1186/s13059-015-0685-2 · Cited by 96
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Bulk, E., Ay, A., Hammadi, M., Ouadid‐Ahidouch, H., Schelhaas, S., Hascher, A., Rohde, C., Thoennissen, N. H., Wiewrodt, R. G., Schmidt, E., et al. (2015) · International Journal of Cancer · doi:10.1002/ijc.29490 · Cited by 96
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Clark, C., Palta, P., Joyce, C. J., Scott, C., Grundberg, E., Deloukas, P., Palotie, A. V., & Coffey, A. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050233 · Cited by 94
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Tomé-García, J., Erfani, P., Nudelman, G., Tsankov, A. M., Katsyv, I., Tejero, R., Zhang, B., Walsh, M. J., Friedel, R. H., Zaslavsky, E., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06258-2 · Cited by 91
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Chung, J.-H., Karkhanis, V. A., Tae, S., Yan, F., Smith, P. L., Ayers, L. W., Agostinelli, C., Pileri, S. A., Denis, G. V., Baiocchi, R. A., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.510669 · Cited by 97
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Sahai, V., Kumar, K., Knab, L. M., Chow, C. R., Raza, S. S., Bentrem, D. J., Ebine, K., & Munshi, H. G. (2014) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-13-0925 · Cited by 98
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Guillamot, M., Cimmino, L., & Aifantis, I. (2016) · Trends in cancer · doi:10.1016/j.trecan.2015.12.006 · Cited by 96
Cai, Y., Tsai, H.-C., Yen, R.-W. C., Zhang, Y. W., Kong, X., Wang, W., Xia, L., & Baylin, S. B. (2017) · Genome Research · doi:10.1101/gr.208108.116 · Cited by 89
Self-citationChu, B. F., Karpenko, M., Liu, Z., Aimiuwu, J., Villalona-Calero, M. A., Chan, K. K. L., Grever, M. R., & Otterson, G. A. (2012) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-012-1986-8 · Cited by 90
de Vries, N. A., Hulsman, D., Akhtar, W., de Jong, J., Miles, D. C., Blom, M., van Tellingen, O., Jonkers, J., & van Lohuizen, M. (2015) · Cell Reports · doi:10.1016/j.celrep.2014.12.028 · Cited by 93
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Nagaraju, G. P., Zhu, S., Wen, J., Farris, A. B., Adsay, V. N., Diaz, R., Snyder, J. P., Shoji, M., & El‐Rayes, B. F. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.08.002 · Cited by 91
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Jeusset, L. M., & McManus, K. J. (2019) · Cells · doi:10.3390/cells8020165 · Cited by 95
Adam, S., Anteneh, H., Hornisch, M., Wagner, V., Lu, J., Radde, N. E., Bashtrykov, P., Song, J., & Jeltsch, A. (2020) · Nature Communications · doi:10.1038/s41467-020-17531-8 · Cited by 88
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Osawa, T., Tsuchida, R., Muramatsu, M., Shimamura, T., Wang, F., Suehiro, J., Kanki, Y., Wada, Y., Yuasa, Y., Aburatani, H., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-3231 · Cited by 88
Tian, X., Zhang, S., Liu, H., Zhang, Y., Blair, C., Mercola, D., Sassone‐Corsi, P., & Zi, X. (2013) · Current Cancer Drug Targets · doi:10.2174/1568009611313050007 · Cited by 90
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Wang, P., Wang, Y., Chen, X., Shen, Z., Cao, H., Zhang, Y., Yu, J., Zhu, J., Lu, Y., & Fang, J. (2012) · Cancer Science · doi:10.1111/j.1349-7006.2012.02292.x · Cited by 85
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Kim, W., Holcomb, T., Januario, T., Du, P., Evangelista, M., Kartha, N., Iniguez, L. A., Soriano, R. H., Huw, L. Y., Stern, H. M., et al. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-2635-t · Cited by 86
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Markopoulos, G. S., Roupakia, E., Marcu, K. B., & Kolettas, E. (2019) · Cells · doi:10.3390/cells8101143 · Cited by 84
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Pajares, M. J., Alemany-Cosme, E., Goñi, S., Bandrés, E., Palanca-Ballester, C., & Sandoval, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147350 · Cited by 82
Ren, J., Li, N., Pei, S., Lian, Y., Li, L., Peng, Y., Liu, Q., Guo, J., Wang, X., Han, Y., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci153167 · Cited by 85
Insights into the epigenetic mechanisms controlling pancreatic carcinogenesis
McCleary‐Wheeler, A. L., Lomberk, G. A., Weiß, F. U., Schneider, G., Fabbri, M., Poshusta, T. L., Dusetti, N., Baumgart, S., Iovanna, J., Ellenrieder, V., et al. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.10.005 · Cited by 86
Noreen, F., Röösli, M., Gaj, P., Pietrzak, J., Weis, S., Urfer, P., Reguła, J., Schär, P., & Truninger, K. (2014) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/dju161 · Cited by 83
Wolff, F., Leisch, M., Greil, R., Risch, A., & Pleyer, L. (2017) · Cell Communication and Signaling · doi:10.1186/s12964-017-0168-z · Cited by 85
Epigenomics of cancer – emerging new concepts
Hassler, M. R., & Egger, G. (2012) · Biochimie · doi:10.1016/j.biochi.2012.05.007 · Cited by 85
Targeting epigenetic regulators for cancer therapy
Wee, S., Dhanak, D., Li, H., Armstrong, S. A., Copeland, R. A., Sims, R. J., Baylin, S. B., Liu, X. S., & Schweizer, L. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12356 · Cited by 81
Self-citationGevensleben, H., Holmes, E. E., Goltz, D., Dietrich, J., Sailer, V., Ellinger, J., Dietrich, D., & Kristiansen, G. (2016) · Oncotarget · doi:10.18632/oncotarget.13161 · Cited by 82
Crosstalk of intracellular post-translational modifications in cancer
Wu, Z., Huang, R., & Yuan, L. (2019) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2019.108138 · Cited by 81
The “virgin birth”, polyploidy, and the origin of cancer
Erenpreisa, J. A., Salmiņa, K., Huna, A., Jackson, T., Vázquez‐Martín, A., & Cragg, M. S. (2014) · Oncoscience · doi:10.18632/oncoscience.108 · Cited by 83
Reactivation of endogenous retroviral elements via treatment with DNMT- and HDAC-inhibitors
Daskalakis, M., Brocks, D., Sheng, Y.-H., Islam, S., Ressnerova, A., Assenov, Y., Milde, T., Oehme, I., Witt, O., Goyal, A., et al. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1442623 · Cited by 90
New insights into prostate cancer stem cells
Chen, X., Rycaj, K., Liu, X., & Tang, D. G. (2013) · Cell Cycle · doi:10.4161/cc.23721 · Cited by 80
DNA methylation, microRNAs, and their crosstalk as potential biomarkers in hepatocellular carcinoma
Anwar, S. L. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i24.7894 · Cited by 79
Epigenetics of breast cancer: Modifying role of environmental and bioactive food compounds
Romagnolo, D. F., Daniels, K. D., Grunwald, J. T., Ramos, S. A., Propper, C. R., & Selmin, O. I. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201501063 · Cited by 82
Assi, R. E., Kantarjian, H. M., Ravandi, F., & Daver, N. G. (2017) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000401 · Cited by 80
Methylation Dynamics of RASSF1A and Its Impact on Cancer
Malpeli, G., Innamorati, G., Decimo, I., Bencivenga, M., Kamdje, A. H. N., Perris, R., & Bassi, C. (2019) · Cancers · doi:10.3390/cancers11070959 · Cited by 79
An update on colorectal cancer microenvironment, epigenetic and immunotherapy
Jin, K., Ren, C., Liu, Y., Lan, H., & Wang, Z. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107041 · Cited by 79
Xi, Y., Lin, Y., Guo, W., Wang, X., Zhao, H., Miao, C., Liu, W., Liu, Y., Liu, T., Luo, Y., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00873-8 · Cited by 79
Epigenetic reprogramming in cancer: From diagnosis to treatment
Costa, P. M. S., Sales, S. L. A., Pinheiro, D. P., Pontes, L. Q., Maranhão, S. S., Pessoa, C., Furtado, G. P., & Furtado, C. L. M. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1116805 · Cited by 89
Common features of chromatin in aging and cancer: cause or coincidence?
Zane, L. K., Sharma, V., & Misteli, T. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.07.001 · Cited by 79
Cancer: pathological nuclear reprogramming?
Goding, C. R., Pei, D., & Lü, X. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3781 · Cited by 82
DNA Methyltransferase Inhibitors: Catalysts For Antitumour Immune Responses
Dan, H., Zhang, S., Zhou, Y., & Guan, Q. (2019) · OncoTargets and Therapy · doi:10.2147/ott.s217767 · Cited by 83
Wang, P., Song, Q., Ren, J., Zhang, W., Wang, Y., Zhou, L., Wang, D., Chen, K., Jiang, L., Zhang, B., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abp8704 · Cited by 79
Koues, O. I., Kowalewski, R., Chang, L., Pyfrom, S., Schmidt, J. A., Luo, H., Sandoval, L., Hughes, T. B., Bednarski, J. J., Cashen, A. F., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.12.021 · Cited by 81
DNA Methylation in the Malignant Transformation of Meningiomas
Gao, F., Shi, L., Russin, J. J., Zeng, L., Chang, X., He, S., Chen, T. C., Giannotta, S. L., Weisenberger, D. J., Zada, G., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054114 · Cited by 77
Links between DNA methylation and nucleosome occupancy in the human genome
Collings, C. K., & Anderson, J. N. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-017-0125-5 · Cited by 77
Metadata
- Authors
- Baylin, S. B., & Jones, P. A.
- Affiliations
- Johns Hopkins University (US)
- University of Southern California (US)
- Corresponding author
- Baylin, Stephen B.
- Jones, Peter A.
- Venue
- Nature Reviews Cancer
- Published
- 2011-09-23
- Volume
- 11
- Issue
- 10
- Pages
- 726-734
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- PMC
- PMC3307543
- OpenAlex
- W2041686632
- Cited by
- 2,871
- References
- 166
- Citations by year
- 2026: 105 · 2025: 107 · 2024: 130 · 2023: 148 · 2022: 179 · 2021: 207 · 2020: 175 · 2019: 209 · 2018: 192 · 2017: 233 · 2016: 241 · 2015: 248 · 2014: 288 · 2013: 231 · 2012: 171
- FWCI
- 20.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Entertainment Industry Foundation
- National Institutes of Health
- National Cancer Institute (R01CA043318, R37CA082422)
- National Institute of Environmental Health Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- cancer epigenome, DNA methylation, chromatin, epigenetic therapy, tumor markers, cancer diagnosis and prognosis, tumor progression, DNA packaging, epigenetic enzymes, cancer metabolism, epigenetic mutations
- MeSH terms
- Animals, Humans, Neoplasms, Genome, Epigenesis, Genetic, History, 20th Century, History, 21st Century, Translational Research, Biomedical, Epigenomics
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