Evidence map›Paper›PMID 39259343›Full record

ArticleMolecular biology reports2024

SIRT6 alleviates senescence induced by Porphyromonas gingivalis in human gingival fibroblasts.

Jia Shi, Xin-Yu Hao, Yue Tong, Wen-Bo Qian, Ying Sun

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 citing papers in PubMed.

  1. Review
  2. mBio · 2026
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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

5 authors.

Jia Shi *Department of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China.
Xin-Yu Hao *Department of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China.
Yue TongDepartment of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China.
Wen-Bo QianDepartment of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China.
Ying SunDepartment of Periodontology, The Affiliated Stomatological Hospital of Nanjing Medical University, No. 1 Shanghai Road, Nanjing, 210029, China. ebolasun@njmu.edu.cn.

Funding

Jiangsu Province Capability Improvement Project through Science, Technology and Education-Jiangsu Provincial Research Hospital Cultivation Unit YJXYYJSDW4Jiangsu Provincial Medical Innovation Center CXZX202227Natural Science Foundation of Jiangsu Province BK20231268
6 · The paper itself

Abstract

objectiveBidirectional influences between senescence and inflammation are newly discovered. This study aimed to clarify the roles and mechanism of Porphyromonas gingivalis (P. gingivalis) in exacerbating senescence in human gingival fibroblasts (HGFs).

designSubgingival plaque and gingivae were collected from twenty-four periodontitis patients and eighteen periodontally healthy subjects. Quantities of P. gingivalis in subgingival plaque were explored using real-time PCR and the expressions of p53, p21 and SIRT6 in gingivae were detected by IHC. Moreover, senescence in HGFs was induced by P. gingivalis lipopolysaccharide (LPS) and the expressions of senescence-related β-galactosidase (SA-β-gal), p53, p21 and senescence-associated secretory phenotype (IL-6 and IL-8) with or without treatment by SIRT6 activator UBCS039 were explored by IHC, western blot and ELISA, respectively. In addition, the levels of SIRT6, Nrf2, HO-1 and reactive oxygen species (ROS) were examined by western blot and flow cytometry.

resultsQuantities of P. gingivalis in subgingival plaque and semi-quantitative scores of p53 and p21 in gingivae of periodontitis patients were increased compared with healthy controls (p < 0.05), while SIRT6 score in periodontitis patients was decreased (p < 0.001). Quantities of P. gingivalis were positively correlated with p53 and p21 scores (0.6 < r < 0.9, p < 0.01), and negatively correlated with SIRT6 score (-0.9 < r<-0.6, p < 0.01). Moreover, P. gingivalis LPS increased the levels of SA-β-gal, p53, p21, IL-6, IL-8 and ROS and decreased the levels of SIRT6, Nrf2 and HO-1 in HGFs, which was rescued by UBCS039 (p < 0.05).

conclusionsP. gingivalis LPS could induce senescence of HGFs, which could be reversed by SIRT6 via Nrf2-HO-1 signaling pathway.

Indexed as

Cellular SenescenceFibroblastsGingivaNF-E2-Related Factor 2Porphyromonas gingivalisReactive Oxygen SpeciesSirtuinsAdultCyclin-Dependent Kinase Inhibitor p21FemaleHeme Oxygenase-1HumansInterleukin-6Interleukin-8LipopolysaccharidesMaleCyclin-Dependent Kinase Inhibitor p21Heme Oxygenase-1HMOX1 protein, humanInterleukin-6Interleukin-8LipopolysaccharidesNFE2L2 protein, humanNF-E2-Related Factor 2Reactive Oxygen SpeciesSIRT6 protein, humanSirtuinsTumor Suppressor Protein p53Human gingival fibroblastsLipopolysaccharidePorphyromonas gingivalisSenescenceSIRT6

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Registered trials

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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 Socratic graph.