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Apigenin suppresses the senescence-associated secretory phenotype and paracrine effects on breast cancer cells
Open accessAbstract
Apigenin (4',5,7,-trihydroxyflavone) is a flavonoid found in certain herbs, fruits, and vegetables. Apigenin can attenuate inflammation, which is associated with many chronic diseases of aging. Senescent cells-stressed cells that accumulate with age in mammals-display a pro-inflammatory senescence-associated secretory phenotype (SASP) that can drive or exacerbate several age-related pathologies, including cancer. Flavonoids, including apigenin, were recently shown to reduce the SASP of a human fibroblast strain induced to senesce by bleomycin. Here, we confirm that apigenin suppresses the SASP in three human fibroblast strains induced to senesce by ionizing radiation, constitutive MAPK (mitogen-activated protein kinase) signaling, oncogenic RAS, or replicative exhaustion. Apigenin suppressed the SASP in part by suppressing IL-1α signaling through IRAK1 and IRAK4, p38-MAPK, and NF-κB. Apigenin was particularly potent at suppressing the expression and secretion of CXCL10 (IP10), a newly identified SASP factor. Further, apigenin-mediated suppression of the SASP substantially reduced the aggressive phenotype of human breast cancer cells, as determined by cell proliferation, extracellular matrix invasion, and epithelial-mesenchymal transition. Our results support the idea that apigenin is a promising natural product for reducing the impact of senescent cells on age-related diseases such as cancer.
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“Beside the antioxidant activity, flavonoids have anti-inflammatory, vasodilator, anticoagulant, cardioprotective, anti-diabetic, neuroprotective, and anti-obesity activities, which make them of great interest as anti-aging compounds (Table 3) [228,229,230,231,232,233,234,235,236,237,238,239,240,241,242,243,244,245,246,247,248,249,250,251,252,253,254,255,256,257].”
From The Role of Antioxidants in the Interplay between Oxidative Stress and Senescence (2022) · cites this paper as [237]
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Cites
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982
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
The senescence-associated secretory phenotype: the dark side of tumor suppression
Coppé, J.-P., Desprez, P.-Y., Krtolica, A., & Campisi, J. (2010) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-121808-102144 · Cited by 5,206
Self-citationAging, Cellular Senescence, and Cancer
Campisi, J. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183653 · Cited by 2,954 · cited 2×
“However, because senescent cells accumulate with age, their chronic presence—most likely through the SASP—can drive age-related pathologies, including, ironically, cancer (Campisi 2013, Muñoz-Espín and Serrano 2014, Baker et al. 2016).”
BackgroundSelf-citationNaturally occurring p16Ink4a-positive cells shorten healthy lifespan
Baker, D. J., Childs, B. G., Durik, M., Wijers, M. E., Sieben, C. J., Zhong, J., A. Saltness, R., Jeganathan, K. B., Verzosa, G. C., Pezeshki, A., et al. (2016) · Nature · doi:10.1038/nature16932 · Cited by 2,876
Cellular senescence: from physiology to pathology
Muñoz-Espín, D., & Serrano, M. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3823 · Cited by 2,818
Geroscience: Linking Aging to Chronic Disease
Kennedy, B. K., Berger, S. L., Brunet, A., Campisi, J., Cuervo, A. M., Epel, E. S., Franceschi, C., Lithgow, G. J., Morimoto, R. I., Pessin, J. E., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.039 · Cited by 2,764
Self-citationPersistent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion
Rodier, F., Coppé, J.-P., Patil, C. K., Hoeijmakers, W. A. M., Muñoz, D. P., Raza, S. R., Freund, A., Campeau, E., Davalos, A. R., & Campisi, J. (2009) · Nature Cell Biology · doi:10.1038/ncb1909 · Cited by 2,232
Self-citationD IETARY F LAVONOIDS : Bioavailability, Metabolic Effects, and Safety
Ross, J. A., & Kasum, C. M. (2002) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.22.111401.144957 · Cited by 2,153
NF-κB, Inflammation, and Metabolic Disease
Baker, R. G., Hayden, M. S., & Ghosh, S. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2010.12.008 · Cited by 1,952
Krtolica, A., Parrinello, S., Lockett, S., Desprez, P.-Y., & Campisi, J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211053698 · Cited by 1,730
Self-citationReversal of human cellular senescence: roles of the p53 and p16 pathways
Beauséjour, C. M., Krtolica, A., Galimi, F., Narita, M., Lowe, S. W., Yaswen, P., & Campisi, J. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg417 · Cited by 1,457
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
Self-citationLaberge, R.-M., Sun, Y., Orjalo, A. V., Patil, C. K., Freund, A., Zhou, L., Curran, S. C., Davalos, A. R., Wilson-Edell, K. A., Liu, S., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3195 · Cited by 1,160
Self-citationFreund, A., Patil, C. K., & Campisi, J. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.69 · Cited by 1,039 · cited 11×
“2010), and we showed p38MAPK is important for the SASP of normal human cells (Freund et al. 2011).”
BackgroundMethodInfluentialSelf-citationApigenin: A Promising Molecule for Cancer Prevention
Shukla, S., & Gupta, S. (2010) · Pharmaceutical Research · doi:10.1007/s11095-010-0089-7 · Cited by 834
Orjalo, A. V., Bhaumik, D., Gengler, B. K., Scott, G. K., & Campisi, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905299106 · Cited by 654
Self-citationLiang, Y., Huang, Y.-T., Tsai, S., Lin‐Shiau, S., Chen, C.-F., & Lin, J.-K. (1999) · Carcinogenesis · doi:10.1093/carcin/20.10.1945 · Cited by 574
Brusselmans, K., Vrolix, R., Verhoeven, G., & Swinnen, J. V. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408177200 · Cited by 477
Coppé, J.-P., Patil, C. K., Rodier, F., Krtolica, A., Beauséjour, C. M., Parrinello, S., Hodgson, J. G., Chin, K., Desprez, P.-Y., & Campisi, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009188 · Cited by 455
Self-citationSenescence-associated inflammatory responses: aging and cancer perspectives
Lasry, A., & Ben-Neriah, Y. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.02.009 · Cited by 408
Nicholas, C., Batra, S., Vargo, M. A., Voss, O. H., Gavrilin, M. A., Wewers, M. D., Guttridge, D. C., Grotewold, E., & Doseff, A. I. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.10.7121 · Cited by 342
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 · cited 11×
“…screening a library of FDA-approved compounds for ability to regulate the secretion of IL-6 (Laberge et al. 2012a), a prominent component of the human and mouse SASP (Coppe et al. 2008; Coppe et al. 2010), we identified apigenin as significantly more active than the vehicle (DMSO) control.”
BackgroundMethodInfluentialGupta, S., Afaq, F., & Mukhtar, H. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.5672 · Cited by 270
Anti-inflammatory activity of structurally related flavonoids, Apigenin, Luteolin and Fisetin
Funakoshi‐Tago, M., Nakamura, K., Tago, K., Mashino, T., & Kasahara, T. (2011) · International Immunopharmacology · doi:10.1016/j.intimp.2011.03.012 · Cited by 264
Epithelial-Mesenchymal Transition Induced by Senescent Fibroblasts
Laberge, R.-M., Awad, P., Campisi, J., & Desprez, P.-Y. (2012) · Cancer Microenvironment · doi:10.1007/s12307-011-0069-4 · Cited by 255
Self-citationWay, T., Kao, M., & Lin, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m305529200 · Cited by 244
Glucocorticoids suppress selected components of the senescence‐associated secretory phenotype
Laberge, R., Zhou, L., Sarantos, M. R., Rodier, F., Freund, A., de Keizer, P. L. J., Liu, S., Demaria, M., Cong, Y., Kapahi, P., et al. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00818.x · Cited by 229
Self-citationLim, H., Park, H., & Kim, H. P. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.06.013 · Cited by 205
Shukla, S., & Gupta, S. (2007) · Cell Cycle · doi:10.4161/cc.6.9.4146 · Cited by 189
Gradolatto, A., Basly, J. P., Bergès, R., Teyssier, C., Chagnon, M., Siess, M. H., & Lavier, M.-C. C. (2004) · Drug Metabolism and Disposition · doi:10.1124/dmd.104.000893 · Cited by 179
Kim, M. H. (2003) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10543 · Cited by 168
Ser276 Phosphorylation of NF-kB p65 by MSK1 Controls SCF Expression in Inflammation
Reber, L. L., Vermeulen, L., Haegeman, G., & Frossard, N. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004393 · Cited by 156
Ruiz, P. A., & Haller, D. (2006) · Journal of Nutrition · doi:10.1093/jn/136.3.664 · Cited by 147
Osada, M., Imaoka, S., & Funae, Y. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.08.036 · Cited by 124
Suppression of cell cycle progression by flavonoids: dependence on the aryl hydrocarbon receptor
Reiners, J. J. (1999) · Carcinogenesis · doi:10.1093/carcin/20.8.1561 · Cited by 108
Li, R.-R., Pang, L., Du, Q., Shi, Y., Dai, W., & Kai-sheng, Y. (2010) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923970903420566 · Cited by 79
Duarte, S., Arango, D., Parihar, A., Hamel, P. P., Yasmeen, R., & Doseff, A. I. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140917664 · Cited by 77
Kang, O., Lee, J. H., & Kwon, D. (2010) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2010.538851 · Cited by 60
Apigenin decreases cell viability and telomerase activity in human leukemia cell lines
Jayasooriya, R. G. P. T., Kang, S.-H., Kang, C., Choi, Y. H., Moon, D., Hyun, J. W., Chang, W. Y., & Kim, G. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.05.024 · Cited by 57
Age-Dependent Changes in CXC Chemokine Ligand 10 Serum Levels in Euthyroid Subjects
Antonelli, A., Rotondi, M., Fallahi, P., Romagnani, P., Ferrari, S. M., Ferrannini, E., & Serio, M. (2005) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2005.25.547 · Cited by 23
Research works printed but not linked: 1
- Funakoshi-Tago M, Nakamura K, Tago K, Mashino T, Kasahara T (2011b) Anti-inflammatory activity of structurally related flavonoids, apigenin, luteolin and fisetin. Int Immunopharmacol 11:1150–1159 · DOI
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Metadata
- Authors
- Perrott, K. M., Wiley, C. D., Desprez, P.-Y., & Campisi, J.
- Affiliations
- Buck Institute for Research on Aging (US)
- California Pacific Medical Center (US)
- Corresponding author
- Campisi, Judith
- Venue
- GeroScience
- Published
- 2017-04
- Volume
- 39
- Issue
- 2
- Pages
- 161-173
- ISSN
- 2152-4041 (ISSN-L)
- 2509-2715
- 2509-2723
- PMC
- PMC5411372
- OpenAlex
- W2604407819
- Cited by
- 163
- References
- 42
- Citations by year
- 2026: 8 · 2025: 21 · 2024: 28 · 2023: 18 · 2022: 17 · 2021: 19 · 2020: 22 · 2019: 15 · 2018: 10 · 2017: 5
- FWCI
- 9.92
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- GeroScience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- SENS Research Foundation (BC2010)
- National Institute on Aging (AG009909, AG017242)
- Topics
- Health Sciences › Medicine › Pharmacology (medical) › Flavonoids in Medical Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Biochemistry (medical) › Phytochemicals and Antioxidant Activities
- Keywords
- apigenin, senescence-associated secretory phenotype, cellular senescence, flavonoids, breast cancer, IRAK1, IRAK4, p38 MAPK, NF-κB, CXCL10, paracrine effects, replicative senescence, oncogenic Ras, MAPK signaling, extracellular matrix invasion, epithelial-mesenchymal transition, inflammation, aging
- MeSH terms
- Breast Neoplasms, Female, Fibroblasts, Humans, Phenotype, Signal Transduction, Interleukin-6, NF-kappa B, Cellular Senescence, Cell Culture Techniques, Apigenin, p38 Mitogen-Activated Protein Kinases, Cell Proliferation, Interleukin-1alpha, Interleukin-1 Receptor-Associated Kinases
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