Evidence map›Paper›PMID 41104943›Full record

ArticleJournal of periodontology2026

Upregulation of senescence-associated gene expression levels in human gingival tissue affected by periodontitis.

Su Jung Kim, Chandni Batra, Hiroki Yoshii, Yusuke Hamada, Yasuyoshi Ueki, George J Eckert, Vanchit John, Mizuho Kittaka

Abstract read
In one paragraph

Article in Journal of periodontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. The Role of Cellular Senescence in Oral Health and Disease.International journal of molecular sciences · 2026
    Review
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Su Jung KimDepartment of Periodontology, Indiana University School of Dentistry, Indianapolis, Indiana, USA.
Chandni BatraDepartment of Periodontology, Indiana University School of Dentistry, Indianapolis, Indiana, USA.
Hiroki YoshiiDepartment of Oral Biology, Dental College of Georgia, Augusta, Georgia, USA.
Yusuke HamadaSection of Periodontics, University of California Los Angeles School of Dentistry, Los Angeles, California, USA.
Yasuyoshi UekiDepartment of Biomedical Science and Applied Sciences, Indiana University School of Dentistry, Indianapolis, Indiana, USA.
George J EckertDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine and Richard M. Fairbanks School of Public Health, Indianapolis, Indiana, USA.
Vanchit JohnDepartment of Periodontology, Indiana University School of Dentistry, Indianapolis, Indiana, USA.
Mizuho KittakaDepartment of Oral Biology, Dental College of Georgia, Augusta, Georgia, USA.

Funding

Senescent periodontal ligament cells as a potential therapeutic target for age-associated periodontitisR01DE034757 · NIDCR · AUGUSTA UNIVERSITY · PI Mizuho Kittaka · 2025 to 2026
$771k
Osteocytes-bacteria interaction via NOD1 as a mechanism of bone loss in periodontitisR03DE034787 · NIDCR · AUGUSTA UNIVERSITY · PI KITTAKA, MIZUHO · 2025 to 2025
$322k
The role of cellular senescence in bone loss and recovery in periodontal diseaseR03DE032101 · NIDCR · INDIANA UNIVERSITY INDIANAPOLIS · PI KITTAKA, MIZUHO · 2023 to 2024
$313k
American Academy of Implant Dentistry (AAID)Augusta University Dental College of GeorgiaIndiana University School of DentistryNIDCR NIH HHS R01 DE034757NIDCR NIH HHS R01DE034757NIDCR NIH HHS R03 DE032101NIDCR NIH HHS R03DE032101NIDCR NIH HHS R03 DE034787NIDCR NIH HHS R03DE034787
6 · The paper itself

Abstract

backgroundAccumulation of senescent cells is increasingly recognized as a mechanism of aging and is considered an attractive therapeutic target for various age-associated diseases. The prevalence and severity of periodontitis increase with age, and preclinical studies have demonstrated that senescent cells could be a potential therapeutic target for age-associated periodontitis. However, clinical data linking cellular senescence and periodontitis are limited.

methodsGingival tissues affected with periodontitis and healthy controls were collected from patients with or without periodontitis in a cross-sectional study. RNA isolated from these samples was analyzed for senescence gene expression by quantitative polymerase chain reaction (qPCR) assays. The associations of the gene expression levels with periodontal diagnosis, presence or absence of attachment loss or bleeding on probing, and age were examined. Additionally, we analyzed the expression of senescence genes in the gingival tissues of mice with or without ligature-induced periodontitis.

resultsA total of 54 human gingival tissue samples were included in the study. Among the genes analyzed, p16, TP53, MMP2, and MMP14 exhibited significantly higher expression in the periodontitis group compared to the control group. Furthermore, these genes were associated with clinical signs of periodontitis, such as bleeding score and attachment loss at diagnosis. There were no statistically significant positive correlations between gene expression levels and age. The ligature-induced periodontitis significantly increased expression levels of p16 and other senescence genes in mouse gingival tissues.

conclusionGene expression analysis indicates the accumulation of senescent cells in gingival tissue affected with periodontitis, supporting the concept that senotherapeutics could be effective in treating periodontitis. PLAIN LANGUAGE SUMMARY: Biological stressors cause cells to age, known as cellular senescence. These senescent cells play a significant role in age-related diseases and are considered a key target for treatment. Periodontitis, a gum disease, damages the tissues that support teeth and is a leading cause of tooth loss worldwide. When people get older, they have a higher chance of being affected by periodontitis. Studies using animal models have shown that the accumulation of senescent cells may be driving periodontitis in older individuals. Therefore, targeting senescent cells may be a potential treatment approach for periodontitis. However, clinical evidence showing the accumulation of senescent cells in gum tissue affected with periodontitis is limited. This study aimed to investigate whether periodontitis is accompanied by senescent cell accumulation in the gum tissue by examining gene expression in tissues with and without periodontitis. A total of 54 human gum tissues (27 healthy and 27 diseased) were collected during gum surgeries. Our analysis found that four genes related to cellular senescence (p16, TP53, MMP2, and MMP14) were significantly higher in samples affected with periodontitis. This indicates that senescent cells accumulate in diseased gum tissue. Additionally, results from an animal experiment suggested that being affected with gum disease may be a mechanism accelerating cellular aging in the gum tissue. The findings support the concept that targeting senescent cells would be an effective approach to treat gum disease.

Indexed as

Cellular SenescenceGingivaPeriodontitisAdultAgedAnimalsCross-Sectional StudiesFemaleGene ExpressionHumansMaleMatrix Metalloproteinase 2MiceMiddle AgedUp-RegulationMatrix Metalloproteinase 2cellular senescencegene expressiongingival tissuemouse ligature‐induced periodontitisperiodontitis

Identifiers

PMID41104943
PMCPMC12614813

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.