Literature DB >> 31305507

SA-β-Galactosidase-Based Screening Assay for the Identification of Senotherapeutic Drugs.

Heike Fuhrmann-Stroissnigg1, Fernando E Santiago2, Diego Grassi1, YuanYuan Ling1, Laura J Niedernhofer2, Paul D Robbins3.   

Abstract

Cell senescence is one of the hallmarks of aging known to negatively influence a healthy lifespan. Drugs able to kill senescent cells specifically in cell culture, termed senolytics, can reduce the senescent cell burden in vivo and extend healthspan. Multiple classes of senolytics have been identified to date including HSP90 inhibitors, Bcl-2 family inhibitors, piperlongumine, a FOXO4 inhibitory peptide and the combination of Dasatinib/Quercetin. Detection of SA-β-Gal at an increased lysosomal pH is one of the best characterized markers for the detection of senescent cells. Live cell measurements of senescence-associated β-galactosidase (SA-β-Gal) activity using the fluorescent substrate C12FDG in combination with the determination of the total cell number using a DNA intercalating Hoechst dye opens the possibility to screen for senotherapeutic drugs that either reduce overall SA-β-Gal activity by killing of senescent cells (senolytics) or by suppressing SA-β-Gal and other phenotypes of senescent cells (senomorphics). Use of a high content fluorescent image acquisition and analysis platform allows for the rapid, high throughput screening of drug libraries for effects on SA-β-Gal, cell morphology and cell number.

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Year:  2019        PMID: 31305507     DOI: 10.3791/58133

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  6 in total

Review 1.  The Achilles' heel of cancer survivors: fundamentals of accelerated cellular senescence.

Authors:  Shameel Shafqat; Evelyn Arana Chicas; Areez Shafqat; Shahrukh K Hashmi
Journal:  J Clin Invest       Date:  2022-07-01       Impact factor: 19.456

2.  CD44+ and CD133+ Non-Small Cell Lung Cancer Cells Exhibit DNA Damage Response Pathways and Dormant Polyploid Giant Cancer Cell Enrichment Relating to Their p53 Status.

Authors:  Margarita Pustovalova; Taisia Blokhina; Lina Alhaddad; Anna Chigasova; Roman Chuprov-Netochin; Alexander Veviorskiy; Gleb Filkov; Andreyan N Osipov; Sergey Leonov
Journal:  Int J Mol Sci       Date:  2022-04-28       Impact factor: 6.208

Review 3.  Molecular mechanisms and cardiovascular implications of cancer therapy-induced senescence.

Authors:  Ibrahim Y Abdelgawad; Karim T Sadak; Diana W Lone; Mohamed S Dabour; Laura J Niedernhofer; Beshay N Zordoky
Journal:  Pharmacol Ther       Date:  2020-12-01       Impact factor: 12.310

4.  Mild exacerbation of obesity- and age-dependent liver disease progression by senolytic cocktail dasatinib + quercetin.

Authors:  Marco Raffaele; Kristina Kovacovicova; Jan Frohlich; Oriana Lo Re; Sebastiano Giallongo; Jude A Oben; Martin Faldyna; Lenka Leva; Antonino Giulio Giannone; Daniela Cabibi; Manlio Vinciguerra
Journal:  Cell Commun Signal       Date:  2021-04-08       Impact factor: 5.712

Review 5.  Senolytic drugs: from discovery to translation.

Authors:  J L Kirkland; T Tchkonia
Journal:  J Intern Med       Date:  2020-08-04       Impact factor: 13.068

6.  Mesenchymal stem cell-derived extracellular vesicles reduce senescence and extend health span in mouse models of aging.

Authors:  Akaitz Dorronsoro; Fernando E Santiago; Diego Grassi; Tianpeng Zhang; Ruenn Chai Lai; Sara J McGowan; Luise Angelini; Mitra Lavasani; Lana Corbo; Aiping Lu; Robert W Brooks; Marta Garcia-Contreras; Donna B Stolz; Antonio Amelio; Siddaraju V Boregowda; Mohammad Fallahi; Adrian Reich; Camillo Ricordi; Donald G Phinney; Johnny Huard; Sai Kiang Lim; Laura J Niedernhofer; Paul D Robbins
Journal:  Aging Cell       Date:  2021-03-16       Impact factor: 9.304

  6 in total

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