TY - JOUR
T1 - Cellular senescence and cardiovascular diseases
T2 - moving to the "heart" of the problem
AU - Evangelou, Konstantinos
AU - Vasileiou, Panagiotis V. S.
AU - Papaspyropoulos, Angelos
AU - Hazapis, Orsalia
AU - Petty, Russell
AU - Demaria, Marco
AU - Gorgoulis, Vassilis G.
N1 - Funding Information:
We acknowledge support by the: National Public Investment Program of the Ministry of Development and Investment / General Secretariat for Research and Technology, in the framework of the Flagship Initiative to address SARS-CoV-2 (2020ΣΕ01300001); the European Regional Development Fund of the European Union and Greek national funds through the Operational Program Competitiveness, Entrepreneurship and Innovation, under the call RESEARCH – CREATE – INNOVATE (project code: T2EDK-02939); H. Pappas donation; Hellenic Foundation for Research and Innovation (HFRI) grants no. 775 and 3782; Welfare Foundation for Social & Cultural Sciences, Athens, Greece (KIKPE); NKUA SARG grant 70/3/8916. Panagiotis V.S. Vasileiou has been awarded a Hellenic Cardiological Society Scholarship for Research in the field of cellular senescence. A.P. is co-funded by the Foundation for Education and European Culture (IPEP)
Publisher Copyright:
© 2022, Physiological Reviews.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Cardiovascular diseases (CVDs) constitute the prime cause of global mortality, with an immense impact on patient quality of life and disability. Clinical evidence has revealed a strong connection between cellular senescence and worse cardiac outcomes in the majority of CVDs concerning both ischemic and nonischemic cardiomyopathies. Cellular senescence is characterized by cell cycle arrest accompanied by alterations in several metabolic pathways, resulting in morphological and functional changes. Metabolic rewiring of senescent cells results in marked paracrine activity, through a unique secretome, often exerting deleterious effects on neighboring cells. Here, we recapitulate the hallmarks and key molecular pathways involved in cellular senescence in the cardiac context and summarize the different roles of senescence in the majority of CVDs. In the last few years, the possibility of eliminating senescent cells in various pathological conditions has been increasingly explored, giving rise to the field of senotherapeutics. Therefore, we additionally attempt to clarify the current state of this field with a focus on cardiac senescence and discuss the potential of implementing senolytics as a treatment option in heart disease.
AB - Cardiovascular diseases (CVDs) constitute the prime cause of global mortality, with an immense impact on patient quality of life and disability. Clinical evidence has revealed a strong connection between cellular senescence and worse cardiac outcomes in the majority of CVDs concerning both ischemic and nonischemic cardiomyopathies. Cellular senescence is characterized by cell cycle arrest accompanied by alterations in several metabolic pathways, resulting in morphological and functional changes. Metabolic rewiring of senescent cells results in marked paracrine activity, through a unique secretome, often exerting deleterious effects on neighboring cells. Here, we recapitulate the hallmarks and key molecular pathways involved in cellular senescence in the cardiac context and summarize the different roles of senescence in the majority of CVDs. In the last few years, the possibility of eliminating senescent cells in various pathological conditions has been increasingly explored, giving rise to the field of senotherapeutics. Therefore, we additionally attempt to clarify the current state of this field with a focus on cardiac senescence and discuss the potential of implementing senolytics as a treatment option in heart disease.
KW - Cardiovascular diseases
KW - stress
KW - cellular senescence
KW - senotherapeutics
KW - cardiovascular diseases
UR - http://www.scopus.com/inward/record.url?scp=85141005676&partnerID=8YFLogxK
U2 - 10.1152/physrev.00007.2022
DO - 10.1152/physrev.00007.2022
M3 - Review article
C2 - 36049114
SN - 0031-9333
VL - 103
SP - 609
EP - 647
JO - Physiological Reviews
JF - Physiological Reviews
IS - 1
ER -