Preview

Acta Biomedica Scientifica

Advanced search

Cellular senescence and senescence biomarkers: pathophysiological significance, molecular mechanisms, and clinical perspectives

https://doi.org/10.29413/ABS.2026-11.1.11

Abstract

Population aging is accompanied by an increasing incidence of age-related diseases, including oncological, neurodegenerative, and cardiovascular pathologies. One of the key mechanisms underlying these processes is cellular senescence - an irreversible arrest of cell division while maintaining metabolic activity. With age, such cells accumulate, contribute to chronic inflammation, and disrupt tissue homeostasis. In this context, the development of reliable biomarkers of cellular aging is becoming particularly relevant.

The aim. To provide an overview of current data on cellular senescence: consider its concept and significance in pathophysiology, key molecular mechanisms, various types of senescence biomarkers and methods for their detection, as well as the clinical significance of these biomarkers, difficulties and prospects for their application.

Materials and methods. Search and analysis of domestic and international scientific sources were conducted using databases such as PubMed, eLibrary.ru, Scopus, and Google Scholar, as well as open-access resources available covering the period from 2011 to 2025.

Results and discussion. This study presents a comprehensive classification of cellular aging biomarkers, encompassing genetic, epigenetic, protein, endocrine, and metabolic indicators. Genetic markers include telomere shortening, while epigenetic markers involve alterations in DNA methylation and the formation of specific heterochromatin foci. Protein biomarkers are characterized by increased expression of cell cycle inhibitors and pro-inflammatory molecules secreted by senescent cells. Endocrine markers comprise levels of dehydroepiandrosterone sulfate, cortisol, and insulin-like growth factor 1. Metabolic markers include elevated β-galactosidase activity, lipofuscin accumulation, and increased concentrations of reactive oxygen species. The clinical relevance of these biomarkers lies in their utility for assessing biological age, stratifying the risk of age-related diseases, and monitoring the efficacy of geroprotective and senolytic interventions.

Conclusion. The necessity of a comprehensive approach to the assessment of cellular aging is substantiated, integrating molecular, metabolic, and functional parameters. The review highlights the prospects for developing a standardized panel of biomarkers (an “aging passport”) for implementation in clinical practice and personalized medicine.

About the Authors

I. Kh. Borukaeva
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Irina Kh. Borukaeva - Dr. Sc. (Med.), head of the Department of Normal and Pathological Human Physiology Kabardino-Balkarian State University named after H.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



Z. F. Kharaeva
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Zaira F. Kharaeva - Dr. Sc. (Med.), professor, head of the Department of Microbiology, Virology and Immunology of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



I. K. Tkhabisimova
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Irina K. Tkhabisimova - Cand. Sc. (Med.), associate professor, head of the Department of general medical training and medical rehabilitation of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



A. B. Khadzugov
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Artur B. Khadzugov - Cand. Sc. (Med.), associate professor of the Department of General medical training and medical rehabilitation of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



T. A. Umov
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Tembulat A. Umov - 5th year student of the General Medicine specialty of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



B. M. Shogenov
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Batyrbek M. Shogenov - 5th year student of the General Medicine specialty of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



A. M. Kunizhev
Kabardino-Balkarian State University named after H.M. Berbekov
Russian Federation

Akhmed M. Kunizhev - 5th year student of the General Medicine specialty of the Kabardino-Balkarian State University named after Kh.M. Berbekov.

Chernyshevsky St., 173, Nalchik, 360004, Kabardino-Balkarian Republic



References

1. Muthamil S, Kim HY, Jang HJ, Lyu JH, Shin UC, Go Y, et al. Biomarkers of Cellular Senescence and Aging: Current State-of-the-Art, Challenges and Future Perspectives. Adv Biol (Weinh). 2024; 8(9): e2400079. doi: 10.1002/adbi.202400079

2. Wagner KD, Wagner N. The Senescence Markers p16INK4A, p14ARF/p19ARF, and p21 in Organ Development and Homeostasis. Cells. 2022; 11(12): 1966. doi: 10.3390/cells11121966

3. Ogrodnik M. Cellular aging beyond cellular senescence: Markers of senescence prior to cell cycle arrest in vitro and in vivo. Aging Cell. 2021; 20(4): e13338. doi: 10.1111/acel.13338

4. Xiang X, Dong C, Zhou L, Liu J, Rabinowitz ZM, Zhang Y, et al. Novel PET Imaging Probe for Quantitative Detection of Senescence In Vivo. J Med Chem. 2024; 67(7): 5924-5934. doi: 10.1021/acs.jmedchem.4c00179

5. López-Otín C, Blasco MA, Partridge L, Serrano M, Kroeamer G. Hallmarks of aging: An expanding universe. Cell. 2023; 186(2): 243-278. doi: 10.1021/10.1016/j.cell.2022.11.001

6. Lu KJ, Sheu JR, Teng RD, Jayakumar T, Chung CL, Hsieh CY. Ability of Local Clearance of Senescent Cells in Ipsilateral Hemisphere to Mitigate Acute Ischemic Brain Injury in Mice. Int J Biol Sci. 2023; 19(9): 2835-2847. doi: 10.7150/ijbs.84060

7. Eltokhi A, Catterall WA, Gamal El-Din TM. Cell-cycle arrest at the G1/S boundary enhances transient voltage-gated ion channel expression in human and insect cells. Cell Rep Methods. 2023; 3(9): 100559. doi: 10.1016/j.crmeth.2023.100559.

8. Shay JW, Wright WE. Hayflick, his limit, and cellular ageing. Nat Rev Mol Cell Biol. 2000; 1(1): 72-6. doi: 10.1038/35036093

9. Kwon J, Bakhoum SF. The Cytosolic DNA-Sensing cGAS-STING Pathway in Cancer. Cancer Discov. 2020; 10(1): 26-39. doi: 10.1158/2159-8290.CD-19-0761

10. Zeng PH, Yin WJ. The cGAS/STING signaling pathway: a cross-talk of infection, senescence and tumors. Cell Cycle. 2023; 22(1): 38-56. doi: 10.1080/15384101.2022.2109899

11. Kang C, Xu Q, Martin TD, Li MZ, Demaria M, Aron L, et al. The DNA damage response induces inflammation and senescence by inhibiting autophagy of GATA4. Science. 2015; 349(6255): aaa5612. doi: 10.1126/science.aaa5612

12. Huang W, Hickson LJ, Eirin A, Kirkland JL, Lerman LO. Cellular senescence: the good, the bad and the unknown. Nat Rev Nephrol. 2022; 18(10): 611-627. doi: 10.1038/s41581-022-00601-z

13. Wu H, Deng C, Zheng X, Huang Y, Chen C, Gu H. Identification of a novel cellular senescence-related ln-cRNA signature for prognosis and immune response in osteosarcoma. Transl Cancer Res. 2024; 13(7): 3742-3759. doi: 10.21037/tcr-24-163

14. Zhang L, Pitcher LE, Yousefzadeh MJ, Niedernhofer LJ, Robbins PD, Zhu Y. Cellular senescence: a key therapeutic target in aging and diseases. J Clin Invest. 2022; 132(15): e158450. doi: 10.1172/JCI158450

15. Engeland K. Cell cycle regulation: p53-p21-RB signaling. Cell Death Differ. 2022; 29: 946-960. doi: 10.1038/s41418-022-00988-z

16. Lai L, Shin GY, Qiu H. The Role of Cell Cycle Regulators in Cell Survival-Dual Functions of Cyclin-Dependent Kinase 20 and p21. Int J Mol Sci. 2020; 21: 8504. doi: 10.3390/ijms21228504

17. Han X, Lei Q, Xie J, Liu H, Li J, Zhang X, et al. Potential Regulators of the Senescence-Associated Secretory Phenotype During Senescence and Aging. J Gerontol A Biol Sci Med Sci. 2022; 77(11): 2207-2218. doi: 10.1093/gerona/glac097

18. Schwartz RE, Conboy IM. Non-Intrinsic, Systemic Mechanisms of Cellular Senescence. Cells. 2023; 12(24): 2769. doi: 10.3390/cells12242769

19. Loo TM, Miyata K, Tanaka Y, Takahashi A. Cellular senescence and senescence-associated secretory phenotype via the cGAS-STING signaling pathway in cancer. Cancer Sci. 2020; 111(2): 304-311. doi: 10.1111/cas.14266

20. Di Micco R, Krizhanovsky V, Baker D, d'Adda di Fagagna F. Cellular senescence in ageing: from mechanisms to therapeutic opportunities. Nat Rev Mol Cell Biol. 2021; 22(2): 75-95. doi: 10.1038/s41580-020-00314-w

21. St Sauver JL, Weston SA, Atkinson EJ, Mc Gree ME, Mielke MM, White TA, et al. Biomarkers of cellular senescence and risk of death in humans. Aging Cell. 2023; 22(12): e14006. doi: 10.1111/acel.14006

22. Kirichenko TV, Markina YuV, Markin AM, Eremin II, Deev RV. Senescent cells: a therapeutic target in correction of aging. Regenerative Biotechnologies, Preventive, Digital and Predictive Medicine. 2024; 1(3): 53-63. (In Russ.). doi: 10.17116/rbpdpm2024103153

23. Sienkiewicz M, Sroka K, Binienda A, Jurk D, Fichna J. A new face of old cells: An overview about the role of senescence and telomeres in inflammatory bowel diseases. Ageing Res Rev. 2023; 91: 102083. doi: 10.1016/j.arr.2023.102083

24. Yan J, Chen S, Yi Z, Zhao R, Zhu J, Ding S, et al. The role of p21 in cellular senescence and aging-related diseases. Mol Cells. 2024; 47(11): 100113. doi: 10.1016/j.mo-cell.2024.100113

25. Swift ML, Sell C, Azizkhan-Clifford J. DNA damage-induced degradation of Sp1 promotes cellular senescence. Geroscience. 2022; 44(2): 683-698. doi: 10.1007/s11357-021-00456-5

26. Billimoria R, Bhatt P. Senescence in cancer: Advances in detection and treatment modalities. Biochem Pharmacol. 2023; 215: 115739. doi: 10.1016/j.bcp.2023.115739

27. Ya J, Bayraktutan U. Senolytics and Senomorphics Targeting p38MAPK/NF-KB Pathway Protect Endothelial Cells from Oxidative Stress-Mediated Premature Senescence. Cells. 2024; 13(15): 1292. doi: 10.3390/cells13151292

28. Xiao FH, Yu Q, Deng ZL, Yang K, Ye Y, Ge MX, et al. ETS1 acts as a regulator of human healthy aging via de-creasing ribosomal activity. Sci Adv. 2022; 8(17): eabf2017. doi: 10.1126/sciadv.abf2017

29. Ni M, Peng W, Wang X, Li J. Role of Aging in Ulcerative Colitis Pathogenesis: A Focus on ETS1 as a Promising Biomarker. J Inflamm Res. 2025; 18: 1839-1853. doi: 10.2147/JIR.S504040

30. Reimann M, Lee S, Schmitt CA. Cellular senescence: Neither irreversible nor reversible. J Exp Med. 2024; 221(4): e20232136. doi: 10.1084/jem.20232136

31. Wang B, Han J, Elisseeff JH, Demaria M. The senescence-associated secretory phenotype and its physiological and pathological implications. Nat Rev Mol Cell Biol. 2024; 25(12): 958-978. doi: 10.1038/s41580-024-00727-x

32. Mohamad Kamal NS, Safuan S, Shamsuddin S, Foroozandeh P. Aging of the cells: Insight into cellular senescence and detection Methods. Eur J Cell Biol. 2020; 99(6): 151108. doi: 10.1016/j.ejcb.2020.151108

33. Saul D, Kosinsky RL, Atkinson EJ, Doolittle ML, Zhang X, LeBrasseur NK, et al. A new gene set identifies senescent cells and predicts senescence-associated pathways across tissues. Nat Commun. 2022; 13(1): 4827. doi: 10.1038/s41467-022-32552-1

34. Huo S, Tang X, Chen W, Gan D, Guo H, Yao Q, et al. Epigenetic regulations of cellular senescence in osteoporosis. Ageing Res Rev. 2024; 99: 102235. doi: 10.1016/j.arr.2024.102235

35. Ghosh M, Saha S, Li J, Montrose DC, Martinez LA. p53 engages the cGAS/STING cytosolic DNA sensing pathway for tumor suppression. Mol Cell. 2023; 83(2): 266-280. e6. doi: 10.1016/j.molcel.2022.12.023

36. Wang XH, Gao JW, Bao JP, Zhu L, Xie ZY, Chen L, et al. GATA4 promotes the senescence of nucleus pulposus cells via NF-KB pathway. Arch Gerontol Geriatr. 2022; 101: 104676. doi: 10.1016/j.archger.2022.104676

37. Gong H, Chen H, Xiao P, Huang N, Han X, Zhang J, et al. miR-146a impedes the anti-aging effect of AMPK via NAMPT suppression and NAD+/SIRT inactivation. Signal Transduct Target Ther. 2022; 7(1): 66. doi: 10.1038/s41392-022-00886-3

38. Sławińska N, Krupa R. Molecular Aspects of Senescence and Organismal Ageing-DNA Damage Response, Telomeres, Inflammation and Chromatin. Int J Mol Sci. 2021; 22(2): 590. doi: 10.3390/ijms22020590

39. Miller TE, El Farran CA, Couturier CP, Chen Z, D'Antonio JP, Verga J, et al. Programs, origins and immunomodulatory functions of myeloid cells in glioma. Nature. 2025; 640(8060): 1072-1082. doi: 10.1038/s41586-025-08633-8

40. Wang M, Wang H, Wang X, Shen Y, Zhou D, Jiang Y. Identification of cellular senescence-related genes and immune cell infiltration characteristics in intervertebral disc degeneration. Front Immunol. 2024; 15: 1439976. doi: 10.3389/fimmu.2024.1439976

41. Pańczyszyn A, Boniewska-Bernacka E, Goc A. The role of telomeres and telomerase in the senescence of postmitotic cells. DNA Repair (Amst). 2020; 95: 102956. doi: 10.1016/j.dnarep.2020.102956

42. Margiotti K, Monaco F, Fabiani M, Mesoraca A, Giorlandino C. Epigenetic Clocks: In Aging-Related and Complex Diseases. Cytogenet Genome Res. 2023; 163(5-6): 247-256. doi: 10.1159/000534561

43. Raj K, Horvath S. Current perspectives on the cellular and molecular features of epigenetic ageing. Exp Biol Med (Maywood). 2020; 245(17): 1532-1542. doi: 10.1177/1535370220918329

44. Olan I, Handa T, Narita M. Beyond SAHF: An integrative view of chromatin compartmentalization during senescence. Curr Opin Cell Biol. 2023; 83: 102206. doi: 10.1016/j.ceb.2023.102206

45. Nicetto D, Zaret KS. Role of H3K9me3 heterochromatin in cell identity establishment and maintenance. Curr Opin Genet Dev. 2019; 55: 1-10. doi: 10.1016/j.gde.2019.04.013.

46. Olan I, Handa T, Narita M. Beyond SAHF: An integrative view of chromatin compartmentalization during senescence. Curr Opin Cell Biol. 2023; 83: 102206. doi: 10.1016/j.ceb.2023.102206

47. Marcozzi S, Bigossi G, Giuliani ME, Giacconi R, Piacenza F, Cardelli M, et al. Cellular senescence and frailty: a comprehensive insight into the causal links. Geroscience. 2023; 45(6): 3267-3305. doi: 10.1007/s11357-023-00960-w

48. Chandra A, Lagnado AB, Farr JN, Doolittle M, Tchkonia T, Kirkland JL, et al. Targeted clearance of p21-but not p16-positive senescent cells prevents radiation-induced osteoporosis and increased marrow adiposity. Aging Cell. 2022; 21(5): e13602. doi: 10.1111/acel.13602

49. Cummings SR, Lui LY, Zaira A, Mau T, Fielding RA, Atkinson EJ, et al. Biomarkers of cellular senescence and major health outcomes in older adults. Geroscience. 2024. doi: 10.1007/s11357-024-01474-9. Epub ahead of print. Erratum in: Geroscience. 2025. doi: 10.1007/s11357-025-01619-4

50. Fielding RA, Atkinson EJ, Aversa Z, White TA, Heeren AA, Achenbach SJ, et al. Associations between biomarkers of cellular senescence and physical function in humans: observations from the lifestyle interventions for elders (LIFE) study. Geroscience. 2022; 44(6): 2757-2770. doi: 10.1007/s11357-022-00685-2

51. Madaeva IM, Kurashova NA, Titova EV, et al. Growth Differentiation Factor GDF 15 (“Protein of Senility”) under Conditions of Oxidative Stress and Intermittent Nocturnal Hypoxia in Patients with Sleep Apnea Syndrome. Adv Gerontol. 2024; 14: 61-67. doi: 10.1134/S2079057024600447

52. Artemenkov AA. Age-dependent disregulation of the immune response in humans. Medical Immunology (Russia). 2021;23(5):1005-1016. (In Russ.). doi: 10.15789/1563-0625-ADO-2192

53. Liu Y, Gu JJ, Yang L, Tsai PC, Guo Y, Xue K, et al. The adhesion molecule ICAM-1 in diffuse large B-cell lymphoma post-rituximab era: relationship with prognostic importance and rituximab resistance. Aging (Albany NY). 2020; 13(1): 181-193. doi: 10.18632/aging.202180

54. Wang Q, Wang X, Liu B, Ma S, Zhang F, Sun S, et al. Aging induces region-specific dysregulation of hormone synthesis in the primate adrenal gland. Nat Aging. 2024; 4(3): 396-413. doi: 10.1038/s43587-024-00588-1

55. Knezevic E, Nenic K, Milanovic V, Knezevic NN. The Role of Cortisol in Chronic Stress, Neurodegenerative Diseases, and Psychological Disorders. Cells. 2023; 12(23): 2726. doi: 10.3390/cells12232726

56. Gao X, Li F, Liu B, Wang Y, Wang Y, Zhou H. Cellular Senescence in Adrenocortical Biology and Its Disorders. Cells. 2021; 10(12): 3474. doi: 10.3390/cells10123474

57. Dowery R, Benhamou D, Benchetrit E, Harel O, Nevelsky A, Zisman-Rozen S, et al. Peripheral B cells repress B-cell regeneration in aging through a TNF-a/IGFBP-1/ IGF-1 immune-endocrine axis. Blood. 2021; 138(19): 1817-1829. doi: 10.1182/blood.2021012428

58. Lee H, Lee SV. Recent Progress in Regulation of Aging by Insulin/IGF-1 Signaling in Caenorhabditis elegans. Mol Cells. 2022; 45(11): 763-770. doi: 10.14348/mol-cells.2022.0097

59. Jauhari A, Baranov SV, Suofu Y, Kim J, Singh T, Yablonska S, et al. Melatonin inhibits cytosolic mitochondrial DNA-induced neuroinflammatory signaling in accelerated aging and neurodegeneration. J Clin Invest. 2020; 130(6): 3124-3136. doi: 10.1172/JCI135026. Erratum in: J Clin Invest. 2021; 131(9): 150328. doi:10.1172/JCI150328

60. Lin LT, Li CJ, Lee YS, Tsui KH. Recombinant Follicle-Stimulating Hormone and Luteinizing Hormone Enhance Mitochondrial Function and Metabolism in Aging Female Reproductive Cells. Int J Mol Sci. 2024; 26(1): 83. doi: 10.3390/ijms26010083

61. Wang Z, Yang T, Liu S, Chen Y. Effects of bone marrow mesenchymal stem cells on ovarian and testicular function in aging Sprague-Dawley rats induced by D-galactose. Cell Cycle. 2020; 19(18): 2340-2350. doi: 10.1080/15384101.2020.1806434

62. Lu W, Feng W, Lai J, Yuan D, Xiao W, Li Y. Role of adipokines in sarcopenia. Chin Med J (Engl). 2023; 136(15): 1794-1804. doi: 10.1097/CM9.0000000000002255

63. Kawakami F, Imai M, Isaka Y, Cookson MR, Maruyama H, Kubo M, et al. LRRK2 negatively regulates glucose tolerance via regulation of membrane translocation of GLUT4 in adipocytes. FEBS Open Bio. 2023; 13(12): 2200-2214. doi: 10.1002/2211-5463.13717

64. Kotolloshi R, Mirzakhani K, Ahlburg J, Kraft F, Pungsrinont T, Baniahmad A. Thyroid hormone induces cellular senescence in prostate cancer cells through induction of DEC1. J Steroid Biochem Mol Biol. 2020; 201: 105689. doi: 10.1016/j.jsbmb.2020.105689

65. Rutledge J, Lehallier B, Zarifkar P, Losada PM, Shahid-Besanti M, Western D, et al. Comprehensive proteomics of CSF, plasma, and urine identify DDC and other biomarkers of early Parkinson's disease. Acta Neuropathol. 2024; 147(1): 52. doi: 10.1007/s00401-024-02706-0

66. Valieva Y, Ivanova E, Fayzullin A, Kurkov A, Igrunkova A. Senescence-Associated в-Galactosidase Detection in Pathology. Diagnostics (Basel). 2022; 12(10): 2309. doi: 10.3390/diagnostics12102309

67. Marzullo M, El Mai M, Ferreira MG. Whole-mount Senescence-Associated Beta-Galactosidase (SA-e-GAL) Activity Detection Protocol for Adult Zebrafish. Bio Protoc. 2022; 12(13): e4457. doi: 10.21769/BioProtoc.4457

68. Cai Y, Zhou H, Zhu Y, Sun Q, Ji Y, Xue A, et al. Elimination of senescent cells by в-galactosidase-targeted prodrug attenuates inflammation and restores physical function in aged mice. Cell Res. 2020; 30(7): 574-589. doi: 10.1038/s41422-020-0314-9

69. Mahmud S, Pitcher LE, Torbenson E, Robbins PD, Zhang L, Dong X. Developing transcriptomic signatures as a biomarker of cellular senescence. Ageing Res Rev. 2024; 99: 102403. doi: 10.1016/j.arr.2024.102403

70. Yu S, Chen M, Xu L, Mao E, Sun S. A senescence-based prognostic gene signature for colorectal cancer and identification of the role of SPP1-positive macrophages in tumor senescence. Front Immunol. 2023; 14: 1175490. doi: 10.3389/fimmu.2023.1175490

71. Evangelou K, Gorgoulis VG. Sudan Black B. The Specific Histochemical Stain for Lipofuscin: A Novel Method to Detect Senescent Cells. Methods Mol Biol. 2017; 1534: 111-119. doi: 10.1007/978-1-4939-6670-7_10

72. Vizioli MG, Liu T, Miller KN, Robertson NA, Gilroy K, Lagnado AB, et al. Mitochondria-to-nucleus retrograde signaling drives formation of cytoplasmic chromatin and inflammation in senescence. Genes Dev. 2020; 34(5-6): 428-445. doi: 10.1101/gad.331272.119

73. Lagnado A, Leslie J, Ruchaud-Sparagano MH, Victorelli S, Hirsova P, Ogrodnik M, et al. Neutrophils induce paracrine telomere dysfunction and senescence in ROS-dependent manner. EMBO J. 2021; 40(9): e106048. doi: 10.15252/embj.2020106048

74. Salameh Y, Bejaoui Y, El Hajj N. DNA Methylation Biomarkers in Aging and Age-Related Diseases. Front Genet. 2020; 11: 171. doi: 10.3389/fgene.2020.00171

75. Kuehnemann C, Wiley CD. Senescent cells at the crossroads of aging, disease, and tissue homeostasis. Aging Cell. 2024; 23(1): e13988. doi: 10.1111/acel.13988

76. Iqbal W, Zhou W. Computational Methods for Single-cell DNA Methylome Analysis. Genomics Proteomics Bioinformatics. 2023; 21(1): 48-66. doi: 10.1016/j.gpb.2022.05.007

77. Mehdizadeh M, Aguilar M, Thorin E, Ferbeyre G, Nattel S. The role of cellular senescence in cardiac disease: basic biology and clinical relevance. Nat Rev Cardiol. 2022; 19(4): 250-264. doi: 10.1038/s41569-021-00624-2

78. Khosla S, Farr JN, Tchkonia T, Kirkland JL. The role of cellular senescence in ageing and endocrine disease. Nat Rev Endocrinol. 2020; 16(5): 263-275. doi: 10.1038/s41574-020-0335-y

79. McHugh D, Duran I, Gil J. Senescence as a therapeutic target in cancer and age-related diseases. Nat Rev Drug Discov. 2025; 24(1): 57-71. doi: 10.1038/s41573-024-01074-4

80. Chambers CR, Ritchie S, Pereira BA, Timpson P. Overcoming the senescence-associated secretory phenotype (SASP): a complex mechanism of resistance in the treatment of cancer. Mol Oncol. 2021; 15(12): 3242-3255. doi: 10.1002/1878-0261.13042


Review

For citations:


Borukaeva I.Kh., Kharaeva Z.F., Tkhabisimova I.K., Khadzugov A.B., Umov T.A., Shogenov B.M., Kunizhev A.M. Cellular senescence and senescence biomarkers: pathophysiological significance, molecular mechanisms, and clinical perspectives. Acta Biomedica Scientifica. 2026;11(1):127-138. (In Russ.) https://doi.org/10.29413/ABS.2026-11.1.11

Views: 481

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2541-9420 (Print)
ISSN 2587-9596 (Online)