» Articles » PMID: 34769049

Biomolecular Evaluation of Piceatannol's Effects in Counteracting the Senescence of Mesenchymal Stromal Cells: A New Candidate for Senotherapeutics?

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Nov 13
PMID 34769049
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Several investigations on senescence and its causative role in aging have underscored the importance of developing senotherapeutics, a field focused on killing senescent cells and/or preventing their accumulation within tissues. Using polyphenols in counteracting senescence may facilitate the development of senotherapeutics given their presence in the human diet, their confirmed tolerability and absence of severe side effects, and their role in preventing senescence and inducing the death of senescent cells. Against that background, we evaluated the effect of piceatannol, a natural polyphenol, on the senescence of mesenchymal stromal cells (MSCs), which play a key role in the body's homeostasis. Among our results, piceatannol reduced the number of senescent cells both after genotoxic stress that induced acute senescence and in senescent replicative cultures. Such senotherapeutics activity, moreover, promoted the recovery of cell proliferation and the stemness properties of MSCs. Altogether, our findings demonstrate piceatannol's effectiveness in counteracting senescence by targeting its associated pathways and detecting and affecting P53-dependent and P53-independent senescence. Our study thus suggests that, given piceatannol's various mechanisms to accomplish its pleiotropic activities, it may be able to counteract any senescent phenotypes.

Citing Articles

Resveratrol and Its Analogues: Anti-ageing Effects and Underlying Mechanisms.

Zhou D, Cheng J, Li J, Wu S, Xiong R, Huang S Subcell Biochem. 2024; 107:183-203.

PMID: 39693025 DOI: 10.1007/978-3-031-66768-8_9.


Arctigenin from Exhibits Antiaging Effects via Autophagy Induction, Antioxidative Stress, and Increase in Telomerase Activity in Yeast.

Chen S, Li Y, Wu E, Li Q, Xiang L, Qi J Antioxidants (Basel). 2024; 13(6).

PMID: 38929123 PMC: 11200627. DOI: 10.3390/antiox13060684.


Identification of a mechanism promoting mitochondrial sterol accumulation during myocardial ischemia-reperfusion: role of TSPO and STAR.

Brehat J, Leick S, Musman J, Su J, Eychenne N, Giton F Basic Res Cardiol. 2024; 119(3):481-503.

PMID: 38517482 DOI: 10.1007/s00395-024-01043-3.


Prognostic and therapeutic potential of senescent stromal fibroblasts in prostate cancer.

Mori J, Elhussin I, Brennen W, Graham M, Lotan T, Yates C Nat Rev Urol. 2023; 21(5):258-273.

PMID: 37907729 PMC: 11058122. DOI: 10.1038/s41585-023-00827-x.


Mesenchymal Stem Cell Senescence during Aging:From Mechanisms to Rejuvenation Strategies.

Jiang X, Li W, Ge L, Lu M Aging Dis. 2023; 14(5):1651-1676.

PMID: 37196126 PMC: 10529739. DOI: 10.14336/AD.2023.0208.


References
1.
Alessio N, Capasso S, Ferone A, Di Bernardo G, Cipollaro M, Casale F . Misidentified Human Gene Functions with Mouse Models: The Case of the Retinoblastoma Gene Family in Senescence. Neoplasia. 2017; 19(10):781-790. PMC: 5577395. DOI: 10.1016/j.neo.2017.06.005. View

2.
Coppe J, Desprez P, Krtolica A, Campisi J . The senescence-associated secretory phenotype: the dark side of tumor suppression. Annu Rev Pathol. 2010; 5:99-118. PMC: 4166495. DOI: 10.1146/annurev-pathol-121808-102144. View

3.
Kirkland J, Tchkonia T . Cellular Senescence: A Translational Perspective. EBioMedicine. 2017; 21:21-28. PMC: 5514381. DOI: 10.1016/j.ebiom.2017.04.013. View

4.
Kao C, Chen L, Chang Y, Yung M, Hsu C, Chen Y . Resveratrol protects human endothelium from H(2)O(2)-induced oxidative stress and senescence via SirT1 activation. J Atheroscler Thromb. 2010; 17(9):970-9. DOI: 10.5551/jat.4333. View

5.
Malavolta M, Bracci M, Santarelli L, Sayeed M, Pierpaoli E, Giacconi R . Inducers of Senescence, Toxic Compounds, and Senolytics: The Multiple Faces of Nrf2-Activating Phytochemicals in Cancer Adjuvant Therapy. Mediators Inflamm. 2018; 2018:4159013. PMC: 5829354. DOI: 10.1155/2018/4159013. View