Evidence map›Paper›PMID 37626297›Full record

ArticleCellular & molecular biology letters2023

CRISPR/Cas13d targeting GZMA in PARs pathway regulates the function of osteoclasts in chronic apical periodontitis.

Tingting Jia, Fang Yuan, Jingqiao Tao, Gang Wang, Xianhua Zhang, Bin Zhang, Hongbo Li

Open access · goldAbstract readLetter
In one paragraph

Article in Cellular & molecular biology letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. CRISPR-epigenetic crosstalk: From bidirectional regulation to therapeutic potential.Computational and structural biotechnology journal · 2025
    Review
  4. Article
  5. Review
  6. CRISPR-Cas9 applications in T cells and adoptive T cell therapies.Cellular & molecular biology letters · 2024
    Review
4 · The record

Corrections and comments

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

7 authors at 2 institutions in 1 country.

Tingting JiaDepartment of Stomatology, The First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Fang YuanDepartment of Oncology, The Fifth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Jingqiao TaoDepartment of Stomatology, Southern Medical Branch of PLA General Hospital, Beijing, China.
Gang WangMedical School of Chinese PLA, Beijing, China.
Xianhua ZhangDepartment of Stomatology, The First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Bin ZhangDepartment of Stomatology, The First Medical Centre, Chinese PLA General Hospital, Beijing, China. binzhangfmmu@163.com.
Hongbo LiDepartment of Stomatology, The First Medical Centre, Chinese PLA General Hospital, Beijing, China. hongbolii@sina.com.
Chinese PLA General Hospital · CNPLA Academy of Military Science · CN

Funding

National Key Research and Development Program of China 2017YFA0106200Project funded by China Postdoctoral Science Foundation 2022M723863
6 · The paper itself

Abstract

Chronic apical periodontitis is a prevalent oral disease characterized by bone loss, and its underlying mechanisms remain unclear. This study aimed to investigate the role and mechanism of the serine protease GZMA in osteoclasts during chronic apical periodontitis. To address this, we employed crRNA/Cas13d to inhibit GZMA expression and examined its impact on osteoclast behavior. Our findings revealed that GZMA plays a significant role in promoting osteoclast cell proliferation while inhibiting cell apoptosis. Additionally, the inhibition of GZMA led to a notable increase in miR-25-3p expression, which, in turn, downregulated the expression of TGF-β. Consequently, the reduction in TGF-β expression led to a decrease in PAR1 expression within the PARs pathway. These results suggest that GZMA might serve as a promising therapeutic target for the treatment of chronic apical periodontitis. Furthermore, our study highlights the potential of targeting GZMA using crRNA/Cas13d as a valuable approach for future therapeutic interventions.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsPeriapical PeriodontitisApoptosisGranzymesHumansOsteoclastsRNA, Guide, CRISPR-Cas SystemsTransforming Growth Factor betaGranzymesGZMA protein, humanRNA, Guide, CRISPR-Cas SystemsTransforming Growth Factor betaChronic apical periodontitisCRISPR/Cas13dGZMAOsteoclast

Identifiers

PMID37626297
PMCPMC10464397
OpenAlexW4386160694

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.