Identification and characterization of Cardiac Glycosides as senolytic compounds

被引:0
作者
Francisco Triana-Martínez
Pilar Picallos-Rabina
Sabela Da Silva-Álvarez
Federico Pietrocola
Susana Llanos
Verónica Rodilla
Enrica Soprano
Pablo Pedrosa
Alba Ferreirós
Marta Barradas
Fernanda Hernández-González
Marta Lalinde
Neus Prats
Cristina Bernadó
Patricia González
María Gómez
Maria P. Ikonomopoulou
Pablo J. Fernández-Marcos
Tomás García-Caballero
Pablo del Pino
Joaquín Arribas
Anxo Vidal
Miguel González-Barcia
Manuel Serrano
María I. Loza
Eduardo Domínguez
Manuel Collado
机构
[1] Health Research Institute of Santiago de Compostela (IDIS),Laboratory of Stem Cells in Cancer and Aging
[2] Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS),Institute for Research in Biomedicine (IRB Barcelona)
[3] BioFarma,Preclinical Research Program
[4] Center for Research in Molecular Medicine and Chronic Diseases (CIMUS),Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS) and Departamento de Física de Partículas
[5] Universidade de Santiago de Compostela,Metabolic Syndrome Group
[6] Health Research Institute of Santiago de Compostela (IDIS),Department of Pulmonology, ICR, Hospital Clinic
[7] The Barcelona Institute of Science and Technology (BIST),Histopathology Unit
[8] DNA Replication Group,Translational Venomics Group
[9] Spanish National Cancer Research Centre (CNIO),Departamento de Ciencias Morfológicas
[10] Vall d´Hebron Institute of Oncology (VHIO) and CIBERONC,undefined
[11] Universidade de Santiago de Compostela,undefined
[12] Madrid Institute for Advanced Studies (IMDEA) in Food,undefined
[13] CEI UAM+CSIC,undefined
[14] Instituto de Investigaciones Biomedicas August Pi i Sunyer (IDIBAPS),undefined
[15] Spanish National Cancer Research Centre (CNIO),undefined
[16] Madrid Institute for Advanced Studies (IMDEA) in Food,undefined
[17] CEI UAM+CSIC,undefined
[18] Facultad de Medicina. USC. Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS),undefined
[19] Catalan Institution for Research and Advanced Studies (ICREA),undefined
[20] CiCLOn,undefined
[21] Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CIMUS),undefined
[22] Universidade de Santiago de Compostela,undefined
[23] Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS),undefined
[24] Servicio de Farmacia,undefined
[25] Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS),undefined
来源
Nature Communications | / 10卷
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摘要
Compounds with specific cytotoxic activity in senescent cells, or senolytics, support the causal involvement of senescence in aging and offer therapeutic interventions. Here we report the identification of Cardiac Glycosides (CGs) as a family of compounds with senolytic activity. CGs, by targeting the Na+/K+ATPase pump, cause a disbalanced electrochemical gradient within the cell causing depolarization and acidification. Senescent cells present a slightly depolarized plasma membrane and higher concentrations of H+, making them more susceptible to the action of CGs. These vulnerabilities can be exploited for therapeutic purposes as evidenced by the in vivo eradication of tumors xenografted in mice after treatment with the combination of a senogenic and a senolytic drug. The senolytic effect of CGs is also effective in the elimination of senescence-induced lung fibrosis. This experimental approach allows the identification of compounds with senolytic activity that could potentially be used to develop effective treatments against age-related diseases.
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  • [11] Yanai H(2011)Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders Nature 479 232-236
  • [12] Fraifeld VE(2007)Cellular senescence in cancer and aging Cell 130 223-233
  • [13] López-Otín C(2012)Cancer cell senescence: a new frontier in drug development Drug Discov. Today 17 269-276
  • [14] Blasco MA(2005)Escape from therapy-induced accelerated cellular senescence in p53-null lung cancer cells and in human lung cancers Cancer Res. 65 2795-2803
  • [15] Partridge L(2002)DNA damage is able to induce senescence in tumor cells in vitro and in vivo Cancer Res. 62 1876-1883
  • [16] Serrano M(2002)A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy Cell 109 335-346
  • [17] Kroemer G(2018)Paracrine roles of cellular senescence in promoting tumourigenesis Br. J. Cancer 118 1283-1288
  • [18] van Deursen JM(2016)SASP: tumor suppressor or promoter? Yes! Trends Cancer 2 676-687
  • [19] Zhu Y(2017)Cellular senescence promotes adverse effects of chemotherapy and cancer relapse Cancer Discov. 7 165-176
  • [20] Armstrong JL(2013)Role of type II pneumocyte senescence in radiation-induced lung fibrosis J. Natl Cancer Inst. 105 1474-1484