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DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions
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had no impact on blood counts or indices. Mutational burden of both genes correlated with X-inactivation skewing but no significant association with age-adjusted telomere length reduction was documented. The discordance between the high prevalence of mutations in these 2 genes and their limited biological impact raise the question of the potential role of dysregulated epigenetic modifiers in normal aging hematopoiesis, which may include support to failing hematopoiesis.
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“Various other systemic effects have been described in association with CH, including chronic obstructive pulmonary disease and other pulmonary disease [16,33,34]”
From Clonal hematopoiesis and inflammation – the perpetual cycle (2023) · cites this paper as [33]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Loss-of-function heterozygous mutations in epigenetic regulators DNMT3A (cytosine methyltransferase) and TET2 (methylcytosine dioxygenase) are the most frequently detected mutations in CHIP, accounting for about 50% to 60% and 10% to 30% of mutations found in CHIP carriers, respectively.1, 2, 3,7,8”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
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In the citing paper
“In the context of CHIP, TET2 mutations show highest clonal expansion rates over time (with an estimated 10% annual growth rate compared with 5% of DNMT3A mutations7,8,10).”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Loss-of-function heterozygous mutations in epigenetic regulators DNMT3A (cytosine methyltransferase) and TET2 (methylcytosine dioxygenase) are the most frequently detected mutations in CHIP, accounting for about 50% to 60% and 10% to 30% of mutations found in CHIP carriers, respectively.1, 2, 3,7,8”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“are predicted to have high expansion rates (10% increase in mean VAF per year1, 2, 3,7)”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
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“many have noted that DNMT3A mutations confer little phenotype on steady state hematopoiesis (Buscarlet et al., 2017)”
From Chronic infection drives Dnmt3a-loss-of-function clonal hematopoiesis via IFNγ signaling (2021) · cites this paper as Buscarlet et al., 2017
In the citing paper
“CHIP itself does not denote a malignancy, nor is it associated with clinically significant alterations in blood counts 28,63.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
In the citing paper
“Other studies have found links between CHIP and chronic obstructive pulmonary disease (COPD) 37,63.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
In the citing paper
“However, CHIP was also strongly linked to smoking in these studies, so the result could be confounded by this association.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
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Citations
Cites
Signatures of mutational processes in human cancer
Initiative, A. P. C. G., Alexandrov, L. B., ICGC Breast Cancer Consortium, ICGC MMML-Seq Consortium, PedBrain, I., Nik-Zainal, S., Wedge, D. C., Aparicio, S. A. J. R., Behjati, S., Biankin, A. V., et al. (2013) · Nature · doi:10.1038/nature12477 · Cited by 9,660
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841
Telomere measurement by quantitative PCR
Cawthon, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.10.e47 · Cited by 3,550
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Genovese, G., Kähler, A. K., Handsaker, R. E., Lindberg, J., Rose, S. A., Bakhoum, S. F., Chambert, K., Mick, E., Neale, B. M., Fromer, M., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1409405 · Cited by 3,531
Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes
Steensma, D. P., Bejar, R., Jaiswal, S., Lindsley, R. C., Sekeres, M. A., Hasserjian, R. P., & Ebert, B. L. (2015) · Blood · doi:10.1182/blood-2015-03-631747 · Cited by 1,971
Age-related mutations associated with clonal hematopoietic expansion and malignancies
Xie, M., Lu, C., Wang, J., McLellan, M. D., Johnson, K. J., Wendl, M. C., McMichael, J. F., Schmidt, H. K., Yellapantula, V., Miller, C. A., et al. (2014) · Nature Medicine · doi:10.1038/nm.3733 · Cited by 1,874
Allen, R. C., Zoghbi, H. Y., Moseley, A., Rosenblatt, H. M., & Belmont, J. W. (1992) · PubMed · Cited by 1,683
The origin and evolution of mutations in acute myeloid leukemia
Welch, J. S., Ley, T. J., Link, D. C., Miller, C. A., Larson, D. E., Koboldt, D. C., Wartman, L. D., Lamprecht, T. L., Liu, F., Xia, J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.023 · Cited by 1,575
Guralnik, J. M., Eisenstaedt, R. S., Ferrucci, L., Klein, H. G., & Woodman, R. C. (2004) · Blood · doi:10.1182/blood-2004-05-1812 · Cited by 1,450
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia
Shlush, L. I., Zandi, S., Mitchell, A., Chen, W. C., Brandwein, J. M., Gupta, V., Kennedy, J. A., Schimmer, A. D., Schuh, A. C., Yee, K. W., et al. (2014) · Nature · doi:10.1038/nature13038 · Cited by 1,443
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Schoeler, K., Aufschnaiter, A., Messner, S., Derudder, E., Herzog, S., Villunger, A., Rajewsky, K., & Labi, V. (2019) · FEBS Journal · doi:10.1111/febs.14934 · Cited by 59
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Shevyrev, D., Tereshchenko, V., Berezina, T. N., & Александрович, Р. С. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065862 · Cited by 58
Clonal hematopoiesis in elderly twins: concordance, discordance, and mortality
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Corces, M. R., Chang, H. Y., & Majeti, R. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00263 · Cited by 56
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Immunomodulation and immunopharmacology in heart failure
Markousis‐Mavrogenis, G., Baumhove, L., Al‐Mubarak, A. A., Aboumsallem, J. P., Bömer, N., Voors, A. A., & van der Meer, P. (2023) · Nature Reviews Cardiology · doi:10.1038/s41569-023-00919-6 · Cited by 51
Grimm, J., Bill, M., Jentzsch, M., Beinicke, S., Häntschel, J., Goldmann, K., Schulz, J. C., Cross, M. A., Franke, G., Behre, G., et al. (2018) · Bone Marrow Transplantation · doi:10.1038/s41409-018-0413-0 · Cited by 46
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Silver, A. J., & Jaiswal, S. (2019) · Advances in cancer research · doi:10.1016/bs.acr.2018.12.003 · Cited by 46
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Kwon, M., Kim, B. S., Yoon, S., Oh, S., & Lee, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136837 · Cited by 42
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Shin, T., Zhou, Y., Chen, S., Cordes, S., Grice, M. Z., Fan, X., Lee, B., Aljanahi, A. A., Hong, S. G., Vaughan, K. L., et al. (2022) · Blood · doi:10.1182/blood.2021014875 · Cited by 39
Gorica, E., Mohammed, S. A., Ambrosini, S., Calderone, V., Costantino, S., & Paneni, F. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.923014 · Cited by 39
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Dai, P., Wu, L. R., Chen, S. X., Wang, M., Cheng, L. Y., Zhang, J. X., Hao, P., Yao, W., Zarka, J. G., Issa, G. C., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26308-6 · Cited by 37
Active DNA demethylation—The epigenetic gatekeeper of development, immunity, and cancer
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Thoms, J. A. I., Beck, D., & Pimanda, J. E. (2019) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22794 · Cited by 33
Ayachi, S., Buscarlet, M., & Busque, L. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.01.008 · Cited by 32
Role of reactive oxygen species in myelodysplastic syndromes
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Pizzi, M., Croci, G. A., Ruggeri, M., Tabano, S. M., Tos, A. P. D., Sabattini, E., & Gianelli, U. (2021) · Cancers · doi:10.3390/cancers13225666 · Cited by 36
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Denicolò, S., Vogi, V., Keller, F., Thöni, S., Eder, S., Heerspink, H. J. L., Rosivall, L., Więcek, A., Mark, P. B., Perco, P., et al. (2022) · Kidney International Reports · doi:10.1016/j.ekir.2022.01.1064 · Cited by 30
Jawad, M. D., Afkhami, M., Ding, Y., Zhang, X., Li, P., Young, K., Xu, M. L., Cui, W., Zhao, Y., Halene, S., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.849376 · Cited by 29
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Torreggiani, S., Castellan, F. S., Aksentijevich, I. A., & Beck, D. B. (2024) · Nature Reviews Rheumatology · doi:10.1038/s41584-024-01168-8 · Cited by 30
Mengel‐From, J., Lindahl‐Jacobsen, R., Nygaard, M., Soerensen, M., Ørstavik, K. H., Hertz, J. M., Andersen‐Ranberg, K., Tan, Q., & Christensen, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-83702-2 · Cited by 29
Ramabadran, R., Wang, J. H., Reyes, J. M., Guzman, A. G., Gupta, S., Rosas, C., Brunetti, L., Gundry, M. C., Tovy, A., Long, H., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01109-9 · Cited by 33
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Hameister, E., Stolz, S. M., Fuhrer, Y., Thienemann, F., Schaer, D. J., Nemeth, J., Schuepbach, R. A., Goede, J. S., Reinhart, S., Schmidt, A. E., et al. (2020) · HemaSphere · doi:10.1097/hs9.0000000000000453 · Cited by 28
Pegliasco, J., Hirsch, P., Marzac, C., Isnard, F., Meniane, J.-C., Deswarte, C., Pellet, P., Lemaitre, C., Leroy, G., Moraes, G. R., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01319-w · Cited by 27
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Nowakowska, M. K., Kim, T., Thompson, M. T., Bolton, K. L., Deswal, A., Lin, S. H., Scheet, P. A., Wehner, M. R., & Nead, K. T. (2022) · American Journal of Hematology · doi:10.1002/ajh.26465 · Cited by 28
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Amorós-Pérez, M., & Fuster, J. J. (2020) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2020.02.008 · Cited by 24
Goldman, E. A., Spellman, P. T., & Agarwal, A. (2023) · Molecular Case Studies · doi:10.1101/mcs.a006251 · Cited by 25
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Lee, J., Godfrey, A. L., & Nangalia, J. (2020) · Blood Reviews · doi:10.1016/j.blre.2020.100708 · Cited by 21
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Christen, F., Hablesreiter, R., Hoyer, K., Hennch, C., Maluck-Böttcher, A., Segler, A., Madadi, A., Frick, M., Bullinger, L., Briest, F., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01469-x · Cited by 22
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Nathan, D. I., Dougherty, M. L., Bhatta, M., Mascarenhas, J. O., & Marcellino, B. K. (2023) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2023.104187 · Cited by 22
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Wang, K., Zhang, W., Yi, L., Zhao, M., Li, P.-Y., Fu, M.-H., Lin, R., Zhu, Y., Li, J., Yang, W., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319364121 · Cited by 24
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Quin, C., DeJong, E. N., McNaughton, A. J. M., Buttigieg, M. M., Basrai, S., Abelson, S., LARCHÉ, M. J., Rauh, M. J., & Bowdish, D. M. E. (2024) · Blood Advances · doi:10.1182/bloodadvances.2023011833 · Cited by 20
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Higa, K. C., & DeGregori, J. V. (2019) · Aging Cell · doi:10.1111/acel.12938 · Cited by 19
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Franch‐Expósito, S., Mehine, M. M., Ptashkin, R. N., Bolton, K. L., Bandlamudi, C., Srinivasan, P., Zhang, L., Goodell, M. A., Gedvilaite, E., Menghrajani, K. N., et al. (2023) · JCO Precision Oncology · doi:10.1200/po.23.00070 · Cited by 21
Shi, Y., Huang, X., Zeng, Y., Zhai, M., Yao, H., Liu, C., Li, B., Gong, S., Yu, Q., Zhuang, J., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.103013 · Cited by 21
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Kaner, J. D., Desai, P. M., Mencia-Trinchant, N., Guzmán, M. L., Roboz, G. J., & Hassane, D. C. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a035675 · Cited by 20
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Newell, L. F., Dunlap, J. B., Gatter, K. M., Bagby, G. C., Press, R. D., Cook, R. J., Fletcher, L. B., Leonard, J. T., Leong, K., Bubalo, J. S., et al. (2021) · American Journal of Transplantation · doi:10.1111/ajt.16635 · Cited by 17
Camus, V., Viennot, M., Lévêque, É., Viailly, P., Tonnelet, D., Veresezan, E., Drieux, F., Etancelin, P., Dubois, S., Stamatoullas, A., et al. (2022) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2021.2010060 · Cited by 17
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He, H., & Wang, J. (2020) · Blood Science · doi:10.1097/bs9.0000000000000063 · Cited by 16
Sega, F. V. D., Palumbo, D., Fortini, F., D’Agostino, Y., Cimaglia, P., Marracino, L., Severi, P., Strianese, O., Tarallo, R., Nassa, G., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-24130-8 · Cited by 20
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Nangalia, J., Mitchell, E., & Green, A. R. (2019) · Blood · doi:10.1182/blood-2018-11-835405 · Cited by 19
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Auerbach, M., & Spivak, J. L. (2019) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2019.03.003 · Cited by 16
Petzer, V., Schwendinger, S., Haschka, D., Vogi, V., Tymoszuk, P., Burkert, F. R., Sahanic, S., Sonnweber, T., Bellmann‐Weiler, R., Löffler‐Ragg, J., et al. (2021) · American Journal of Hematology · doi:10.1002/ajh.26251 · Cited by 16
Gaulin, C., Kelemen, K., & Yi, C. A. (2022) · Life · doi:10.3390/life12081135 · Cited by 16
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van Bladel, D. A. G., Stevens, W. B. C., van den Brand, M., Kroeze, L. I., Groenen, P. J. T. A., van Krieken, J. H., Hebeda, K. M., & Scheijen, B. (2022) · Cancers · doi:10.3390/cancers14133222 · Cited by 15
Huang, J., Xie, J., Wang, Y., Sheng, M., Sun, Y., Chen, P., Rong, S., Yin, D., Wang, Y., Zhu, P., et al. (2025) · Leukemia · doi:10.1038/s41375-025-02542-5 · Cited by 16
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Brown, D. W., Zhou, W., Wang, Y., Jones, K. M., Luo, W., Dagnall, C. L., Teshome, K., Klein, A., Zhang, T., Lin, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32986-7 · Cited by 16
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Isobe, T., Kuciński, I., Barile, M., Wang, X., Hannah, R., Bastos, H. P., Chabra, S., Vijayabaskar, M. S., Sturgess, K., Williams, M., et al. (2023) · Cell Genomics · doi:10.1016/j.xgen.2023.100426 · Cited by 15
Metadata
- Authors
- Buscarlet, M., Provost, S., Zada, Y. F., Barhdadi, A., Bourgoin, V., Lépine, G., Mollica, L., Szuber, N., Dubé, M.-P., & Busque, L.
- Affiliations
- Hôpital Maisonneuve-Rosemont (CA)
- Montreal Heart Institute (CA)
- ORCID
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2017-08-10
- Volume
- 130
- Issue
- 6
- Pages
- 753-762
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2728241634
- Cited by
- 383
- References
- 50
- Citations by year
- 2026: 22 · 2025: 34 · 2024: 37 · 2023: 47 · 2022: 59 · 2021: 55 · 2020: 46 · 2019: 40 · 2018: 34 · 2017: 6
- FWCI
- 26.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Concordia University
- Canadian Institutes of Health Research
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Keywords
- DNMT3A, TET2, clonal hematopoiesis, somatic mutations, X-inactivation skewing, telomere length, epigenetic regulators, genetic susceptibility, mutational burden
- MeSH terms
- DNA Methyltransferase 3A, Age Factors, Aged, Aged, 80 and over, Aging, Blood Cell Count, Clone Cells, DNA (Cytosine-5-)-Methyltransferases, DNA-Binding Proteins, Female, Hematopoiesis, Humans, Male, Middle Aged, Mutation, Proto-Oncogene Proteins, Cohort Studies, Hematologic Neoplasms, Genetic Predisposition to Disease, Dioxygenases, X Chromosome Inactivation, High-Throughput Nucleotide Sequencing, Telomere Homeostasis
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