» Articles » PMID: 15520862

Ink4a/Arf Expression is a Biomarker of Aging

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2004 Nov 3
PMID 15520862
Citations 782
Authors
Affiliations
Soon will be listed here.
Abstract

The Ink4a/Arf locus encodes 2 tumor suppressor molecules, p16INK4a and Arf, which are principal mediators of cellular senescence. To study the links between senescence and aging in vivo, we examined Ink4a/Arf expression in rodent models of aging. We show that expression of p16INK4a and Arf markedly increases in almost all rodent tissues with advancing age, while there is little or no change in the expression of other related cell cycle inhibitors. The increase in expression is restricted to well-defined compartments within each organ studied and occurs in both epithelial and stromal cells of diverse lineages. The age-associated increase in expression of p16INK4a and Arf is attenuated in the kidney, ovary, and heart by caloric restriction, and this decrease correlates with diminished expression of an in vivo marker of senescence, as well as decreased pathology of those organs. Last, the age-related increase in Ink4a/Arf expression can be independently attributed to the expression of Ets-1, a known p16INK4a transcriptional activator, as well as unknown Ink4a/Arf coregulatory molecules. These data suggest that expression of the Ink4a/Arf tumor suppressor locus is a robust biomarker, and possible effector, of mammalian aging.

Citing Articles

Current Methodologies to Assess Cellular Senescence in Cancer.

Laouris P, Munoz-Espin D Methods Mol Biol. 2025; 2906:21-44.

PMID: 40082348 DOI: 10.1007/978-1-0716-4426-3_2.


Restoration of angiogenic capacity in senescent endothelial cells by a pharmacological reprogramming approach.

Kalies K, Knopp K, Koch S, Pilowski C, Wurmbrand L, Sedding D PLoS One. 2025; 20(2):e0319381.

PMID: 40019880 PMC: 11870368. DOI: 10.1371/journal.pone.0319381.


Fetal adnexa-derived allogeneic mesenchymal stem cells for cardiac regeneration: the future trend of cell-based therapy for age-related adverse conditions.

Gorjipour F, Bohloolighashghaei S, Sotoudeheian M, Pazoki Toroudi H Hum Cell. 2025; 38(2):61.

PMID: 39998714 DOI: 10.1007/s13577-025-01190-2.


Regulation of senescence-associated secretory phenotypes in osteoarthritis by cytosolic UDP-GlcNAc retention and O-GlcNAcylation.

Kang D, Lee J, Yook G, Jeong S, Shin J, Kim M Nat Commun. 2025; 16(1):1094.

PMID: 39904978 PMC: 11794700. DOI: 10.1038/s41467-024-55085-1.


Multiplexed single-cell imaging reveals diverging subpopulations with distinct senescence phenotypes during long-term senescence induction.

Sessions G, Loops M, Diekman B, Purvis J Geroscience. 2025; .

PMID: 39849264 DOI: 10.1007/s11357-024-01503-7.


References
1.
Campisi J . Cancer and ageing: rival demons?. Nat Rev Cancer. 2003; 3(5):339-49. DOI: 10.1038/nrc1073. View

2.
Sun L, Lee D, Zhang Q, Xiao W, Raabe E, Meeker A . Growth retardation and premature aging phenotypes in mice with disruption of the SNF2-like gene, PASG. Genes Dev. 2004; 18(9):1035-46. PMC: 406293. DOI: 10.1101/gad.1176104. View

3.
Park I, Qian D, Kiel M, Becker M, Pihalja M, Weissman I . Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells. Nature. 2003; 423(6937):302-5. DOI: 10.1038/nature01587. View

4.
Melk A, Kittikowit W, Sandhu I, Halloran K, Grimm P, Schmidt B . Cell senescence in rat kidneys in vivo increases with growth and age despite lack of telomere shortening. Kidney Int. 2003; 63(6):2134-43. DOI: 10.1046/j.1523-1755.2003.00032.x. View

5.
Chkhotua A, Gabusi E, Altimari A, DErrico A, Yakubovich M, Vienken J . Increased expression of p16(INK4a) and p27(Kip1) cyclin-dependent kinase inhibitor genes in aging human kidney and chronic allograft nephropathy. Am J Kidney Dis. 2003; 41(6):1303-13. DOI: 10.1016/s0272-6386(03)00363-9. View