Cellular Senescence and the Kidney: Potential Therapeutic Targets and Tools

被引:69
作者
Knoppert, Sebastian N. [1 ]
Valentijn, Fioris A. [1 ]
Nguyen, Tri Q. [1 ]
Goldschmeding, Roel [1 ]
Falke, Lucas L. [1 ,2 ]
机构
[1] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Internal Med, Diakonessenhuis, Utrecht, Netherlands
关键词
senescence; chronic kidney disease; kidney fibrosis; senolytics; targeted therapy; HEMATOPOIETIC STEM-CELLS; TUBULAR EPITHELIAL-CELLS; TISSUE GROWTH-FACTOR; SECRETORY PHENOTYPE; REPLICATIVE SENESCENCE; ACCELERATED SENESCENCE; PREMATURE SENESCENCE; IMMUNE SURVEILLANCE; BCL-2; FAMILY; CYCLE ARREST;
D O I
10.3389/fphar.2019.00770
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chronic kidney disease (CKD) is an increasing health burden (affecting approximately 13.4% of the population). Currently, no curative treatment options are available and treatment is focused on limiting the disease progression. The accumulation of senescent cells has been implicated in the development of kidney fibrosis by limiting tissue rejuvenation and through the secretion of pro-fibrotic and pro-inflammatory mediators termed as the senescence-associated secretory phenotype. The clearance of senescent cells in aging models results in improved kidney function, which shows promise for the options of targeting senescent cells in CKD. There are several approaches for the development of "senotherapies", the most rigorous of which is the elimination of senescent cells by the so-called senolytic drugs either newly developed or repurposed for off-target effects in terms of selectively inducing apoptosis in senescent cells. Several chemotherapeutics and checkpoint inhibitors currently used in daily oncological practice show senolytic properties. However, the applicability of such senolytic compounds for the treatment of renal diseases has hardly been investigated. A serious concern is that systemic side effects will limit the use of senolytics for kidney fibrosis. Specifically targeting senescent cells and/ or targeted drug delivery to the kidney might circumvent these side effects. In this review, we discuss the connection between CKD and senescence, the pharmacological options for targeting senescent cells, and the means to specifically target the kidney.
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页数:18
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共 190 条
[1]   The BCL-2 arbiters of apoptosis and their growing role as cancer targets [J].
Adams, Jerry M. ;
Cory, Suzanne .
CELL DEATH AND DIFFERENTIATION, 2018, 25 (01) :27-36
[2]   Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts [J].
Alcorta, DA ;
Xiong, Y ;
Phelps, D ;
Hannon, G ;
Beach, D ;
Barrett, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13742-13747
[3]   Suppression of the senescence-associated secretory phenotype (SASP) in human fibroblasts using small molecule inhibitors of p38 MAP kinase and MK2 [J].
Alimbetov, Dauren ;
Davis, Terence ;
Brook, Amy J. C. ;
Cox, Lynne S. ;
Faragher, Richard G. A. ;
Nurgozhin, Talgat ;
Zhumadilov, Zhaxybay ;
Kipling, David .
BIOGERONTOLOGY, 2016, 17 (02) :305-315
[4]   Increased expression of SIRT2 is a novel marker of cellular senescence and is dependent on wild type p53 status [J].
Anwar, Tarique ;
Khosla, Sanjeev ;
Ramakrishna, Gayatri .
CELL CYCLE, 2016, 15 (14) :1883-1897
[5]   DNA damage detection and repair pathways - Recent advances with inhibitors of checkpoint kinases in cancer therapy [J].
Ashwell, Susan ;
Zabludoff, Sonya .
CLINICAL CANCER RESEARCH, 2008, 14 (13) :4032-4037
[6]   Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging [J].
Baar, Marjolein P. ;
Brandt, Renata M. C. ;
Putavet, Diana A. ;
Klein, Julian D. D. ;
Derks, Kasper W. J. ;
Bourgeois, Benjamin R. M. ;
Stryeck, Sarah ;
Rijksen, Yvonne ;
van Willigenburg, Hester ;
Feijtel, Danny A. ;
van der Pluijm, Ingrid ;
Essers, Jeroen ;
van Cappellen, Wiggert A. ;
van IJcken, Wilfred F. ;
Houtsmuller, Adriaan B. ;
Pothof, Joris ;
de Bruin, Ron W. F. ;
Madl, Tobias ;
Hoeijmakers, Jan H. J. ;
Campisi, Judith ;
de Keizer, Peter L. J. .
CELL, 2017, 169 (01) :132-+
[7]   Naturally occurring p16Ink4a-positive cells shorten healthy lifespan [J].
Baker, Darren J. ;
Childs, Bennett G. ;
Durik, Matej ;
Wijers, Melinde E. ;
Sieben, Cynthia J. ;
Zhong, Jian ;
Saltness, Rachel A. ;
Jeganathan, Karthik B. ;
Verzosa, Grace Casaclang ;
Pezeshki, Abdulmohammad ;
Khazaie, Khashayarsha ;
Miller, Jordan D. ;
van Deursen, Jan M. .
NATURE, 2016, 530 (7589) :184-+
[8]   Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders [J].
Baker, Darren J. ;
Wijshake, Tobias ;
Tchkonia, Tamar ;
LeBrasseur, Nathan K. ;
Childs, Bennett G. ;
van de Sluis, Bart ;
Kirkland, James L. ;
van Deursen, Jan M. .
NATURE, 2011, 479 (7372) :232-U112
[9]   Is DNA damage indispensable for stress-induced senescence? [J].
Bielak-Zmijewska, Anna ;
Mosieniak, Grazyna ;
Sikore, Ewa .
MECHANISMS OF AGEING AND DEVELOPMENT, 2018, 170 :13-21
[10]   Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice [J].
Bitto, Alessandro ;
Ito, Takashi K. ;
Pineda, Victor V. ;
LeTexier, Nicolas J. ;
Huang, Heather Z. ;
Sutlief, Elissa ;
Tung, Herman ;
Vizzini, Nicholas ;
Chen, Belle ;
Smith, Kaleb ;
Meza, Daniel ;
Yajima, Masanao ;
Beyer, Richard P. ;
Kerr, Kathleen F. ;
Davis, Daniel J. ;
Gillespie, Catherine H. ;
Snyder, Jessica M. ;
Treuting, Piper M. ;
Kaeberlein, Matt .
ELIFE, 2016, 5