CDKN2A Gene Expression as a Potential Aging Biomarker in Dogs
- PMID: 33981746
- PMCID: PMC8107359
- DOI: 10.3389/fvets.2021.660435
CDKN2A Gene Expression as a Potential Aging Biomarker in Dogs
Abstract
Describing evolutionary conserved physiological or molecular patterns, which can reliably mark the age of both model organisms and humans or predict the onset of age-related pathologies has become a priority in aging research. The age-related gene-expression changes of the Cyclin Dependent Kinase Inhibitor 2A (CDKN2A) gene have been well-documented in humans and rodents. However, data is lacking from other relevant species, including dogs. Therefore, we quantified the CDKN2A mRNA abundance in dogs of different ages, in four tissue types: the frontal cortex of the brain, temporal muscle, skin, and blood. We found a significant, positive correlation between CDKN2A relative expression values and age in the brain, muscle, and blood; however, no correlation was detected in the skin. The strongest correlation was detected in the brain tissue (CDKN2A/GAPDH: r = 0.757, p < 0.001), similarly to human findings, while the muscle and blood showed weaker, but significant correlation. Our results suggest that CDKN2A might be a potential blood-borne biomarker of aging in dogs, although the validation and optimization will require further, more focused research. Our current results also clearly demonstrate that the role of CDKN2A in aging is conserved in dogs, regarding both tissue specificity and a pivotal role of CDKN2A in brain aging.
Keywords: CDKN2A; aging; biomarker; blood; dog; gene expression.
Copyright © 2021 Sándor, Tátrai, Czeibert, Egyed and Kubinyi.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Similar articles
-
Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases.J Alzheimers Dis. 2021;82(4):1737-1744. doi: 10.3233/JAD-210483. J Alzheimers Dis. 2021. PMID: 34219731 Free PMC article.
-
High CDKN2A/p16 and Low FGFR3 Expression Predict Progressive Potential of Stage pT1 Urothelial Bladder Carcinoma.Clin Genitourin Cancer. 2018 Aug;16(4):248-256.e2. doi: 10.1016/j.clgc.2018.01.009. Epub 2018 Feb 2. Clin Genitourin Cancer. 2018. PMID: 29525349
-
Association between Nrf2 and CDKN2A expression in patients with end-stage renal disease: a pilot study.Aging (Albany NY). 2020 Jul 13;12(16):16357-16367. doi: 10.18632/aging.103685. Epub 2020 Jul 13. Aging (Albany NY). 2020. PMID: 32661200 Free PMC article.
-
Virtually 100% of melanoma cell lines harbor alterations at the DNA level within CDKN2A, CDKN2B, or one of their downstream targets.Genes Chromosomes Cancer. 1998 Jun;22(2):157-63. doi: 10.1002/(sici)1098-2264(199806)22:2<157::aid-gcc11>3.0.co;2-n. Genes Chromosomes Cancer. 1998. PMID: 9598804 Review.
-
The prognostic significance of CDKN2A homozygous deletion in IDH-mutant lower-grade glioma and glioblastoma: a systematic review of the contemporary literature.J Neurooncol. 2020 Jun;148(2):221-229. doi: 10.1007/s11060-020-03528-2. Epub 2020 May 8. J Neurooncol. 2020. PMID: 32385699
Cited by
-
Man's best friend in life and death: scientific perspectives and challenges of dog brain banking.Geroscience. 2021 Aug;43(4):1653-1668. doi: 10.1007/s11357-021-00373-7. Epub 2021 May 10. Geroscience. 2021. PMID: 33970413 Free PMC article. Review.
-
Genes and Longevity of Lifespan.Int J Mol Sci. 2022 Jan 28;23(3):1499. doi: 10.3390/ijms23031499. Int J Mol Sci. 2022. PMID: 35163422 Free PMC article. Review.
-
Toward establishing a worldwide net of canine biobanks.Aging (Albany NY). 2022 Mar 17;14(6):2436-2437. doi: 10.18632/aging.203961. Epub 2022 Mar 17. Aging (Albany NY). 2022. PMID: 35302513 Free PMC article. No abstract available.
-
Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus.Genes (Basel). 2021 Dec 9;12(12):1964. doi: 10.3390/genes12121964. Genes (Basel). 2021. PMID: 34946912 Free PMC article.
References
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous