HDAC2 and 7 down-regulation induces senescence in dermal fibroblasts
Open accessAbstract
. They are characterized by several biomarkers and changes in gene expression that may depend on epigenetic factors, such as histone acetylation, involving a balance between histone acetyltransferases (HATs) and histone deacetylases (HDACs). In this study, we investigate the expression and the role of HDACs on the senescent phenotype of dermal fibroblasts. We report that during replicative senescence, most canonical HDACs are less expressed. Moreover, treatment with SAHA, a histone deacetylase inhibitor (HDACi) also known as Vorinostat, or the specific downregulation of HDAC2 or HDAC7 by siRNA, induces the appearance of senescence biomarkers of dermal fibroblasts. Conversely, the ectopic re-expression of HDAC7 by lentiviral transduction in pre-senescent dermal fibroblasts extends their proliferative lifespan. These results demonstrate that HDACs expression can modulate the senescent phenotype, highlighting their pharmaceutical interest in the context of healthy ageing.
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HDAC7 is modulated during senescence.
“HDAC7 has also been reported to be modulated during senescence and its downregulation promotes senescence in fibroblasts (Warnon et al., 2021).”
From HDACs and the epigenetic plasticity of cancer cells: target the complexity (2022) · cites this paper as Warnon et al., 2021
Downregulation of HDAC7 promotes senescence in fibroblasts.
“HDAC7 has also been reported to be modulated during senescence and its downregulation promotes senescence in fibroblasts (Warnon et al., 2021).”
From HDACs and the epigenetic plasticity of cancer cells: target the complexity (2022) · cites this paper as Warnon et al., 2021
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Cites
Analyzing real-time PCR data by the comparative CT method
Schmittgen, T. D., & Livak, K. J. (2008) · Nature Protocols · doi:10.1038/nprot.2008.73 · Cited by 26,190 · see citing works
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., & Pereira-Smith, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9363 · Cited by 7,477 · see citing works
Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders
Baker, D. J., Wijshake, T., Tchkonia, T., LeBrasseur, N. K., Childs, B. G., van de Sluis, B., Kirkland, J. L., & van Deursen, J. M. (2011) · Nature · doi:10.1038/nature10600 · Cited by 3,670 · cited 1× · see citing works
“Senescent cells, first detected in vitro , are now clearly associated with normal and pathological ageing in vivo [1, 2].”
Cellular Senescence: Defining a Path Forward
Gorgoulis, V., Adams, P. D., Alimonti, A., Bennett, D. C., Bischof, O., Bishop, C., Campisi, J., Collado, M., Evangelou, K., Ferbeyre, G., et al. (2019) · Cell · doi:10.1016/j.cell.2019.10.005 · Cited by 3,225 · cited 1× · see citing works
“…DNA damage, senescence-associated heterochromatin foci (SAHF), resistance to apoptosis, and finally the expression of a particular secretome composed of inflammatory cytokines, chemokines, growth factors and proteases and referred to as the senescence-associated secretory phenotype (SASP) [3, 4].”
A DNA damage checkpoint response in telomere-initiated senescence
Fagagna, F. D. D., Reaper, P. M., Clay-Farrace, L., Fiegler, H., Carr, P., von Zglinicki, T., Saretzki, G., Carter, N. P., & Jackson, S. P. (2003) · Nature · doi:10.1038/nature02118 · Cited by 2,855 · cited 1× · see citing works
“The SASP is mainly regulated at the transcriptional level by several signalling pathways converging to the activation of NF-κB usually in response to DNA double-strands breaks (DSBs) [9].”
An Essential Role for Senescent Cells in Optimal Wound Healing through Secretion of PDGF-AA
Demaria, M., Ohtani, N., Youssef, S. A., Rodier, F., Toussaint, W., Mitchell, J. R., Laberge, R.-M., Vijg, J., Van Steeg, H., Dollé, M. E. T., et al. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.012 · Cited by 2,045 · see citing works
Debacq-Chainiaux, F., Erusalimsky, J. D., Campisi, J., & Toussaint, O. (2009) · Nature Protocols · doi:10.1038/nprot.2009.191 · Cited by 1,668 · see citing works
Self-citationInflammatory networks during cellular senescence: causes and consequences.
Freund, A., Orjalo, A. V., Desprez, P.-Y., & Campisi, J. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.03.003 · Cited by 1,354 · see citing works
A proteomic atlas of senescence-associated secretomes for aging biomarker development
Basisty, N., Kale, A., Jeon, O. H., Kuehnemann, C., Payne, T., Rao, C., Holtz, A., Shah, S., Sharma, V., Ferrucci, L., et al. (2020) · PLOS Biology · doi:10.1371/journal.pbio.3000599 · Cited by 1,348 · see citing works
Senescent cells: an emerging target for diseases of ageing
Childs, B. G., Gluscevic, M., Baker, D. J., Laberge, R.-M., Marquess, D., Dananberg, J., & van Deursen, J. M. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.116 · Cited by 1,284 · see citing works
Histone Deacetylase Inhibitors as Anticancer Drugs
Eckschlager, T., Plch, J., Stiborova, M., & Hrabeta, J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071414 · Cited by 1,206 · see citing works
Lamin B1 loss is a senescence-associated biomarker
Freund, A., Laberge, R.-M., Demaria, M., & Campisi, J. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-10-0884 · Cited by 1,046 · see citing works
Unmasking senescence: context-dependent effects of SASP in cancer
Faget, D. V., Ren, Q., & Stewart, S. A. (2019) · Nature Reviews Cancer · doi:10.1038/s41568-019-0156-2 · Cited by 863 · cited 1× · see citing works
“Nevertheless, some detrimental AGING effects are also associated to the SASP such as the promotion of proliferation, migration and invasion of cancer cells observed in vitro , which could possibly contribute to tumoral development in vivo [6].”
Zhang, H. S., Gavin, M., Dahiya, A., Postigo, A. A., Ma, D., Luo, R. X., Harbour, J. W., & Dean, D. C. (2000) · Cell · doi:10.1016/s0092-8674(00)80625-x · Cited by 658 · see citing works
Rodier, F., Muñoz, D. P., Teachenor, R., Chu, V., Le, O., Bhaumik, D., Coppé, J.-P., Campeau, E., Beauséjour, C. M., Kim, S.-H., et al. (2011) · Journal of Cell Science · doi:10.1242/jcs.071340 · Cited by 535 · see citing works
The cell proliferation antigen Ki-67 organises heterochromatin
Sobecki, M., Mrouj, K., Camasses, A., Parisis, N., Nicolas, É., Llères, D., Gerbe, F., Prieto, S., Krasińska, L., David, A., et al. (2016) · eLife · doi:10.7554/elife.13722 · Cited by 364 · see citing works
Transcriptome signature of cellular senescence
Casella, G., Munk, R., Kim, K. M., Piao, Y., De, S., Abdelmohsen, K., & Gorospe, M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz555 · Cited by 359 · see citing works
Coppé, J.-P., Patil, C. K., Rodier, F., Sun, Y., Muñoz, D. P., Goldstein, J., Nelson, P. S., Desprez, P.-Y., & Campisi, J. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060301 · Cited by 302 · see citing works
Malaquin, N., Martinez, A., & Rodier, F. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.05.010 · Cited by 247 · see citing works
Small molecule compounds that induce cellular senescence.
Petrova, N. V., Velichko, A. K., Razin, S. V., & Kantidze, O. L. (2016) · Aging Cell · doi:10.1111/acel.12518 · Cited by 240 · cited 1× · see citing works
“Treatment of normal or cancer cells with HDACi including sodium butyrate (NaB) or trichostatin A (TSA) induces senescence by displaying mainly a p21 WAF-1 -dependent proliferation arrest [14– 16].”
Waldera Lupa, D. M., Kalfalah, F., Safferling, K., Boukamp, P., Poschmann, G., Volpi, E., Götz-Rösch, C., Bernerd, F., Haag, L., Huebenthal, U., et al. (2015) · Journal of Investigative Dermatology · doi:10.1038/jid.2015.120 · Cited by 224 · see citing works
Pseudo-DNA damage response in senescent cells
Pospelova, T. V., Demidenko, Z. N., Bukreeva, E. I., Pospelov, V. A., Gudkov, A. V., & Blagosklonny, M. V. (2009) · Cell Cycle · doi:10.4161/cc.8.24.10215 · Cited by 200 · see citing works
Pazolli, E., Alspach, E., Milczarek, A., Prior, J., Piwnica-Worms, D., & Stewart, S. A. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-3386 · Cited by 192 · see citing works
Clarke, J., Hsu, A., Yu, Z., Dashwood, R. H., & Ho, E. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201000547 · Cited by 179 · see citing works
Spatial and Temporal Control of Senescence
Ito, Y., Hoare, M., & Narita, M. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.07.004 · Cited by 178 · see citing works
Harms, K. L., & Chen, X. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4397 · Cited by 152 · see citing works
Munro, J., Barr, N. I., Ireland, H., Morrison, V., & Parkinson, E. K. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.01.017 · Cited by 141 · see citing works
Freese, K., Seitz, T., Dietrich, P., Lee, S. M. L., Thasler, W. E., Bosserhoff, A., & Hellerbrand, C. (2019) · Cancers · doi:10.3390/cancers11101587 · Cited by 125 · see citing works
Induction of Polyploidy by Histone Deacetylase Inhibitor: A Pathway for Antitumor Effects
Xu, W., Perez, G., Ngo, L., Gui, C.-Y., & Marks, P. A. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-4608 · Cited by 119 · see citing works
Ryu, C. H., Yoon, W. S., Park, K. Y., Kim, S. M., Lim, J. Y., Woo, J. S., Jeong, C. H., Hou, Y., & Jeun, S. (2012) · BioMed Research International · doi:10.1155/2012/987495 · Cited by 113 · see citing works
Cancer secretome and inflammation: The bright and the dark sides of NF-κB
Capece, D., Verzella, D., Tessitore, A., Alesse, E., Capalbo, C., & Zazzeroni, F. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.004 · Cited by 90 · see citing works
Zhou, H., Cai, Y., Liu, D., Li, M., Sha, Y., Zhang, W., Wang, K., Gong, J., Tang, N., Huang, A., et al. (2018) · Cell Proliferation · doi:10.1111/cpr.12447 · Cited by 85 · see citing works
Transcriptome signature of cellular senescence
Casella, G., Munk, R., Kim, K. M., Piao, Y., De, S., Abdelmohsen, K., & Gorospe, M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz879 · Cited by 83 · see citing works
Siddiqui, H., Solomon, D. A., Gunawardena, R. W., Wang, Y., & Knudsen, E. S. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.21.7719-7731.2003 · Cited by 76 · see citing works
Premature aging/senescence in cancer cells facing therapy: good or bad?
Calvo, L., Ghadaouia, S., Martinez, A., & Rodier, F. (2015) · Biogerontology · doi:10.1007/s10522-015-9593-9 · Cited by 71 · see citing works
p15INK4b in HDAC inhibitor‐induced growth arrest
Hitomi, T., Matsuzaki, Y., Yokota, T., Takaoka, Y., & Sakai, T. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)01186-4 · Cited by 71 · see citing works
Feng, Y., Wang, X., Xu, L., Pan, H., Zhu, S., Liang, Q. Y., Huang, B., & Lü, J. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07128.x · Cited by 68 · see citing works
Histone Deacetylase Inhibitors Promote Apoptosis and Senescence in Human Mesenchymal Stem Cells
Bernardo, G. D., Squillaro, T., Dell’Aversana, C., Miceli, M., Cipollaro, M., Cascino, A., Altucci, L., & Galderisi, U. (2008) · Stem Cells and Development · doi:10.1089/scd.2008.0172 · Cited by 61 · see citing works
HDACs and the senescent phenotype of WI-38 cells
Place, R. F., Noonan, E. J., & Giardina, C. A. (2005) · BMC Cell Biology · doi:10.1186/1471-2121-6-37 · Cited by 57 · see citing works
Zhou, R., Han, L., Li, G., & Tong, T. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp533 · Cited by 57 · see citing works
Luchenko, V. L., Salcido, C. D., Zhang, Y., Agama, K., Komlódi-Pásztor, E., Murphy, R. F., Giaccone, G., Pommier, Y. G., Bates, S. E., & Varticovski, L. (2011) · Cell Cycle · doi:10.4161/cc.10.18.17190 · Cited by 49 · see citing works
Ahn, M., & Yoon, J. (2017) · Journal of Oral Pathology and Medicine · doi:10.1111/jop.12560 · Cited by 47 · see citing works
Groh, T., Hraběta, J., KHALIL, M. A., Doktorová, H., Eckschlager, T., & Stiborová, M. (2015) · International Journal of Oncology · doi:10.3892/ijo.2015.2996 · Cited by 45 · see citing works
HDAC 4 stabilizes SIRT 1 via sumoylation SIRT 1 to delay cellular senescence
Han, X., Niu, J., Zhao, Y., Kong, Q., Tong, T., & Han, L. (2015) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12496 · Cited by 42 · see citing works
Hodge, G. L., Jersmann, H. P. A., Tran, H. B., Roscioli, E., Holmes, M., Reynolds, P. N., & Hodge, S. J. (2015) · Respiratory Research · doi:10.1186/s12931-015-0287-2 · Cited by 42 · see citing works
Adam, S., & Polo, S. E. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.07.017 · Cited by 41 · see citing works
Elknerová, K., Myslivcová, D., Lacinová, Z., Marinov, I., Uherková, L., & Stöckbauer, P. (2010) · Neoplasma · doi:10.4149/neo_2011_01_35 · Cited by 27 · see citing works
Non‐canonical ATM/MRN activities temporally define the senescence secretory program
Malaquin, N., Carrier-Leclerc, A., Martinez, A., Dessureault, M., Ghadaouia, S., Coppé, J., Nadeau, S., Cardin, G., Campisi, J., & Rodier, F. (2020) · EMBO Reports · doi:10.15252/embr.202050718 · Cited by 24 · see citing works
Sodium butyrate induces cellular senescence in neuroblastoma and prostate cancer cells
Lorenz, V., Hessenkemper, W., Rödiger, J., Kyrylenko, S., Kraft, F., & Baniahmad, A. (2011) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci.2011.020 · Cited by 17 · see citing works
Ghayad, S. E., Rammal, G., Sarkis, O., Basma, H., Ghamloush, F., Fahs, A., Karam, M., Harajli, M. H., Rabeh, W., Mouawad, J. E., et al. (2018) · Cancer Biology & Therapy · doi:10.1080/15384047.2018.1529093 · Cited by 17 · see citing works
Shirato, K., Koda, T., Takanari, J., Sakurai, T., Ogasawara, J., Imaizumi, K., Ohno, H., & Kizaki, T. (2018) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2018/5072986 · Cited by 15 · see citing works
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He, X., Hu, W., Zhang, Y., Chen, M., Ding, Y., Yang, H., He, F., Gu, Q., & Shi, Q. (2023) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-023-00501-5 · Cited by 96 · see citing works
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Xiong, J., Dong, L., Lv, Q., Yin, Y., Zhao, J., Ke, Y., Wang, S., Zhang, W., & Wu, M. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1772 · Cited by 55 · see citing works
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Targeting senescent cells to reshape the tumor microenvironment and improve anticancer efficacy
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Giorgio, E. D., Ranzino, L., Tolotto, V., Dalla, E., Burelli, M., Gualandi, N., & Brancolini, C. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06548-2 · Cited by 32 · see citing works
Balamurli, G., Liew, A. Q. X., Tee, W., & Pervaiz, S. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103441 · Cited by 22 · see citing works
CRISPR-based screening identifies XPO7 as a positive regulator of senescence
Li, L., Yang, K., Jing, Y., Fan, Y., Jiang, X., Wang, S., Liu, G., Qu, J. T., Ma, S., & Zhang, W. (2023) · Protein & Cell · doi:10.1093/procel/pwad012 · Cited by 20 · see citing works
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- Authors
- Warnon, C., Bouhjar, K., Ninane, N., Verhoyen, M., Fattaccioli, A., Fransolet, M., Lambert de Rouvroit, C., Poumay, Y., Piel, G., Mottet, D., & Debacq-Chainiaux, F.
- Affiliations
- University of Namur (BE)
- URPHYM, Namur Research Institute for Life Sciences (NARILIS), University of Namur, Namur, Belgium
- University of Liège (BE)
- URBC, Namur Research Institute for Life Sciences (NARILIS), University of Namur, Namur, Belgium
- Venue
- Aging
- Publisher
- Impact Journals, LLC
- Published
- 2021-07-12
- Volume
- 13
- Issue
- 14
- Pages
- 17978-18005
- ISSN
- 1945-4589 (ISSN-L)
- PMC
- PMC8351730
- OpenAlex
- W3182281603
- Cited by
- 25
- References
- 51
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 6 · 2023: 4 · 2022: 1 · 2021: 1
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Aging (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Open Repository and Bibliography (University of Liège) (submittedVersion, other-oa)
- Repository of the University of Namur (submittedVersion, cc-by)
- Funders
- Fonds De La Recherche Scientifique - FNRS
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- HDAC2, HDAC7, histone deacetylase, replicative senescence, dermal fibroblasts, histone acetylation, histone deacetylase inhibitors, vorinostat, siRNA knockdown, senescence biomarkers, healthy aging, epigenetic regulation
- MeSH terms
- Vorinostat, Acetylation, Fibroblasts, Histone Deacetylases, Humans, Skin, Biomarkers, Down-Regulation, Cellular Senescence, Histone Deacetylase 2, Histone Deacetylase Inhibitors
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