Evidence map›Paper›PMID 42473594›Full record

ArticleIranian journal of biotechnology2026

Therapeutic Potential of Ginkgolic Acid C17:1 in Modulating PTEN/mtDNA/TLR9 Axis for Alleviating Chronic Pseudomonas Aeruginosa Infection in Bronchiectasis.

Shuke Rao, Huiyan Jiang, Jieyi Huang, Huafeng Li, Weiliang Yuan, Lichong Chen, Jiamin Xie, Chenli Xie

Abstract read
In one paragraph

Article in Iranian journal of biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Shuke RaoDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.
Huiyan JiangCommunity Health Services Center of Dongguan Humen, Dongguan, Guangdong 523900, China.
Jieyi HuangCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong 510640, China.
Huafeng LiDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.
Weiliang YuanDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.
Lichong ChenDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.
Jiamin XieDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.
Chenli XieDepartment of Pulmonary and Critical Care Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523900, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Objectives: This study aimed to investigate the therapeutic potential of GAC 17:1, a natural compound, in alleviating PA-induced airway injury by targeting the PTEN/mtDNA/TLR9 axis, thereby evaluating its role as a novel biotechnological intervention for immune modulation in bronchiectasis. Materials and Methods: A rat model of chronic PA-induced bronchial injury was established and divided into four groups: Control, PA-infected, PA-infected + GAC 17:1 (PTEN activator, 2 mg.kg Results: PA infection downregulated PTEN, elevated mtDNA/TLR9/NF-κB, increased IL-6/IL-17 and Th17 cells, reduced TGF-β and Tregs, and impaired lung function. Treatment with GAC 17:1, the plant-derived PTEN activator, effectively restored PTEN expression, suppressed mtDNA release and TLR9/NF-κB signaling, rebalanced Th17/Treg immunity, reduced inflammatory cytokines, and significantly improved pulmonary function. Conversely, PTEN inhibition worsened all parameters. Conclusions: This study demonstrates that GAC 17:1, a natural bioactive compound, exerts potent significant effects in PA-related bronchiectasis by activating PTEN and inhibiting the mtDNA/TLR9/NF-κB pathway. Our findings highlight GAC 17:1 as a promising biotechnological candidate for developing plant-derived immunomodulatory therapies against chronic airway infections.

Indexed as

Biotechnological therapyBronchiectasisGinkgolic acid C17:1Immune modulationMitochondrial DNAPhytotherapyPseudomonas aeruginosaPTENToll-like receptor 9

Identifiers

PMID42473594
PMCPMC13380620

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.