Evidence map›Paper›PMID 23494705›Full record

ArticleIrish journal of medical science2013

Arsenic trioxide alleviates airway hyperresponsiveness and promotes apoptosis of CD4+ T lymphocytes: evidence for involvement of the ER stress-CHOP pathway.

K Li, L Zhang, X Xiang, S Gong, L Ma, L Xu, G Wang, Y Liu, X Ji, S Liu and 3 more

Abstract read
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In one paragraph

Article in Irish journal of medical science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Paradoxical effects of arsenic in the lungs.Environmental health and preventive medicine · 2021
    Review
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  9. Arsenic trioxide inhibits lung metastasis of mouse colon cancer via reducing the infiltration of regulatory T cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  10. Arsenical keratosis caused by medication: a case report and literature.International journal of clinical and experimental medicine · 2015
    Article
  11. Association between glucose-regulated protein and neutrophil apoptosis in severe acute pancreatitis.International journal of clinical and experimental pathology · 2015
    Article
  12. Article
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

13 authors at 2 institutions in 1 country.

K LiDepartment of Respiratory Medicine, The Second Xiangya Hospital of Central South University, Changsha, Hunan, 410011, China.
L Zhang
X Xiang
S Gong
L Ma
L Xu
G Wang
Y Liu
X Ji
S Liu
P Chen
H Zeng
J Li
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAsthma is a chronic inflammatory disorder of the airway. Arsenic trioxide (ATO) is an ancient Chinese medicine, which is used to treat psoriasis, asthma, and acute promyelocytic leukemia.

aimWe wanted to research the effect of arsenic trioxide on asthma.

methodsUsing a murine model of asthma, the airway hyperresponsiveness was conducted by the Buxco pulmonary function apparatus. Total cell counts of BALF were counted with a counting chamber. Histopathological analysis of lung tissues was conducted by hematoxylin-eosin or periodic acid-schiff stain. CD4+T cells were purified from the spleen by positive selection, using immunomagnetic beads. Apoptosis measurements were done with Annexin-V/PI staining. Western blot analysis and real time-PCR were performed to assess the expression of C/EBP-homologous protein (CHOP) and glucose-regulated protein 78 (GRP78), respectively. RNA interference was conducted to inhibit the expression of CHOP.

resultsWe found that arsenic trioxide treatment alleviated airway hyperresponsiveness and reduced inflammation of the lung in asthmatic mice. Furthermore, arsenic trioxide treatment promoted apoptosis of CD4+T cells in vivo and in vitro. When CD4+T cells were cultured with arsenic trioxide for 5 h at a concentration of 5 μM, the expression of GRP78 and CHOP was increased. Treatment of CD4+T cells with CHOP siRNA, provided partial resistance to arsenic trioxide-induced apoptosis of CD4+T cells

conclusionsThese data demonstrated that arsenic trioxide can reduce the severity of asthma attacks and induce the apoptosis of CD4+ T cell which the ER stress-CHOP pathway involved.

Indexed as

ApoptosisEndoplasmic Reticulum StressAnimalsAnti-Asthmatic AgentsAnti-Inflammatory AgentsArsenicalsArsenic TrioxideAsthmaBronchial HyperreactivityBronchoalveolar Lavage FluidBronchoconstrictionCD4-Positive T-LymphocytesCells, CulturedDisease Models, AnimalEndoplasmic Reticulum Chaperone BiPFemaleAnti-Asthmatic AgentsAnti-Inflammatory AgentsArsenicalsArsenic TrioxideDdit3 protein, mouseEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHspa5 protein, mouseOxidesTranscription Factor CHOP

Identifiers

PMID23494705
OpenAlexW2049882377

What OpenQuestion holds

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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.