Cited by 61Telomeres, Telomerase, and SenescencePhytochemicals and Antioxidant ActivitiesGenetics, Aging, and Longevity in Model Organisms

Doxorubicin-induced senescence in normal fibroblasts promotes in vitro tumour cell growth and invasiveness: The role of Quercetin in modulating these processes

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Bientinesi, Elisa, Lulli, Matteo, Becatti, Matteo, Ristori, Sara, Margheri, Francesca, Monti, Daniela·2022·Mechanisms of Ageing and Development

Abstract

Ageing is a complex biological phenomenon representing the major risk factor for developing age-related diseases, such as cardiovascular pathologies, neurodegenerative diseases, and cancer. Geroscience, the new vision of gerontology, identifies cellular senescence as an interconnected biological process that characterises ageing and age-related diseases. Therefore, many strategies have been employed in the last years to reduce the harmful effects of senescence, and among these, the most intriguing ones use nutraceutical compounds. Here we show that a pre-treatment with Quercetin, a bioactive flavonoid present in many fruits and vegetables, increasing cellular antioxidant defence, can alleviate Doxorubicin (Doxo)-induced cellular senescence in human normal WI-38 fibroblasts. Furthermore, our work demonstrates that Quercetin pre-treatment, reducing the number of senescent cells and the production of the senescence-associated secretory phenotype (SASP) factors, can decrease the pro-tumour effects of conditioned medium from Doxo-induced senescent fibroblasts on osteosarcoma cells. Overall, our findings are consistent with the hypothesis that targeting senescent cells can be an emerging strategy for cancer treatment, especially in elderly patients, in which senescent cells are already abundant in several tissues and organs.

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Crossref · 10.1016/j.mad.2022.111689

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  • Quercetin (10 μM) induces cell death in mouse bone marrow-derived senescent MSCs and radiation-induced senescent endothelial cells.

    “Notably, a study by Zhu et al. revealed that quercetin (10 μM) could induce cell death in mouse bone marrow-derived senescent MSCs and radiation-induced senescent endothelial cells.”

    From Drug repurposing for cancer therapy (2024) · cites this paper as [240]

  • Pre-treatment with quercetin protects against DOX-induced normal cell senescence by reducing the number of senescent cells and suppressing release of SASP factors.

    “In addition, pre-treatment with quercetin protected against DOX-induced normal cell senescence by reducing the number of senescent cells and suppressing the release of SASP factors.240”

    From Drug repurposing for cancer therapy (2024) · cites this paper as [240]

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References 117 · Cited by 61

Authors
Bientinesi, E., Lulli, M., Becatti, M., Ristori, S., Margheri, F., & Monti, D.
Affiliations
University of Florence (IT)
Corresponding author
Monti, Daniela
Venue
Mechanisms of Ageing and Development
Publisher
Elsevier BV
Published
2022-09
Volume
206
Pages
111689
ISSN
0047-6374 (ISSN-L)
OpenAlex
W4283066332
Cited by
61
References
117
Citations by year
2026: 15 · 2025: 19 · 2024: 16 · 2023: 8 · 2022: 3
FWCI
7.12
Type
journal article
Language
en
Open access
Locations
  • Mechanisms of Ageing and Development (publishedVersion)
  • PubMed (publishedVersion)
  • Florence Research (University of Florence) (submittedVersion, cc-by-nc-nd)
Funders
Università degli Studi di Firenze
Topics
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
  • Health Sciences › Medicine › Biochemistry › Phytochemicals and Antioxidant Activities
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
Keywords
doxorubicin-induced senescence, cellular senescence, quercetin, flavonoids, WI-38 fibroblasts, senescence-associated secretory phenotype, osteosarcoma, tumor invasion, tumour cell growth, conditioned medium, geroscience, nutraceuticals, antioxidant defense, senolytics, chemotherapy-induced senescence
MeSH terms
Aged, Biological Phenomena, Doxorubicin, Fibroblasts, Humans, Neoplasms, Quercetin, Cellular Senescence

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