Evidence map›Paper›PMID 36504067›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2022

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G Sun, X Xu, L Wan, S Nan, Y Wang, L Zhao, H Cheng, K Wang, Y Liu, Y Fang and 2 more

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2022. 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

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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

12 authors at 1 institution in 1 country.

G SunSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
X XuSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
L WanFirst Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230031, China.
S NanSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
Y WangSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
L ZhaoSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
H ChengResearch and Technology Center, Anhui University of Chinese Medicine, Hefei 230012, China.
K WangResearch and Technology Center, Anhui University of Chinese Medicine, Hefei 230012, China.
Y LiuSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
Y FangFirst Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230031, China.
L SunSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
J ZhuSchool of Chinese Medicine, Anhui University of Chinese Medicine, Hefei 230012, China.
Anhui University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo study the regulatory effect of

methodsCCK8 assay was used to determine the optimal concentration and treatment time of JBT for inhibiting the viability of RA- FLS. The effect of freeze-dried powder of JBT, RAPA, or both on morphology of the autophagosomes in RA-FLS was observed under transmission electron microscope, and the changes in the number of autophagosomes and autolysosomes were observed with autophagy double-labeled adenovirus experiment. RT-qPCR and Western blotting were used to detect the expression levels of the related indicators.

resultsThe results of CCK8 assay showed that treatment with 0.5 mg/mL JBT for 12 h produced the optimal effect for inhibiting RA-FLS viability. Observation with transmission electron microscope and the results of the autophagy double-labeled adenovirus experiment both showed the presence of a small number of autophagosomes in control RA-FLS group, and treatment with JBT significantly increased the number of autophagosomes and lowered the number of autophagolysosomes in the cells. Compared with the control cells and the cells treated with JBT or RAPA alone, the cells treated with both JBT and RAPA showed significantly decreased mRNA levels of PI3K, Akt and mTOR (

conclusionJBT can inhibit the survival rate of RA-FLS and increase the level of autophagy possibly through a mechanism that down-regulates PI3K/Akt/mTOR signaling pathway.

Indexed as

Arthritis, RheumatoidSynoviocytesAdenoviridaeAutophagyFibroblastsHumansPhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesMTOR protein, humanPhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesautophagyCheng's Juanbi Decoctionfibroblast-like synoviocytesPI3K/Akt/mTOR

Identifiers

PMID36504067
PMCPMC9742788
OpenAlexW4311665655

What OpenQuestion holds

Textmetadata
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.