Evidence map›Paper›PMID 26261584›Full record

ArticleInternational journal of clinical and experimental pathology2015

ER stress related factor ATF6 and caspase-12 trigger apoptosis in neonatal hypoxic-ischemic encephalopathy.

Luran Liu, Chang Liu, Yuting Lu, Lina Liu, Yan Jiang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.7field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The role of lymphocytes in neonatal encephalopathy.Brain, behavior, & immunity - health · 2021
    Review
  6. Therapeutic Potential and Main Methods of Obtaining Selenium Nanoparticles.International journal of molecular sciences · 2021
    Review
  7. Mechanism of CaBiology · 2021
    Article
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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

5 authors at 1 institution in 1 country.

Luran LiuThe Fourth Affiliated Hospital of Harbin Medical University Haerbin 150001, China.
Chang LiuThe Fourth Affiliated Hospital of Harbin Medical University Haerbin 150001, China.
Yuting LuThe Fourth Affiliated Hospital of Harbin Medical University Haerbin 150001, China.
Lina LiuThe Fourth Affiliated Hospital of Harbin Medical University Haerbin 150001, China.
Yan JiangThe Fourth Affiliated Hospital of Harbin Medical University Haerbin 150001, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The specific and available markers proteins of neonatal hypoxic-ischemic encephalopathy (HIE) injury are correlated with disease severity and the disability in childhood. Exploring the mechanism of HIE is very helpful to the targeted therapeutic approach in clinical. This study aims to explore the cell death-related proteins or biomarkers that plays roles in the HIE injury. In this study, 15 patients were included the 487 autopsies patients performed at the Department of Pathology. The lactate dehydrogenase (LDH) assay was used to detect the cell viability of NGF-differentiated PC12 cell. TUNEL assay was employed to examine the apoptotic cells in embedded slides samples. Three ER stress-related protein, including ATF6, p-Perk and IRE-1 were investigated using Western blot assay for the ER stress examination. The apoptosis associated caspase-12 and CHOP protein were detected by Western blot. The results indicated that LDH activity of living cells during hypoxia was significantly enhanced to 45% and 64% after 8 hours and 24 hours. The TUNEL results showed that plenty of the PC12 cells became the positive staining cells when treated with 0.1% O2 hypoxia. ER stress UPR pathway protein, cleaved ATF6, was increased significantly when treated with 0.1% O2 compared with the cells treated with 20% O2. Furthermore, the caspase 12 activation was triggered when the cells treated with the 0.1% O2. In conclusion, apoptosis is served as an important factor that triggers the HIE brain injury through cleaving the ATF6 and caspase-12 ER stress-related protein.

Indexed as

ApoptosisEndoplasmic Reticulum StressActivating Transcription Factor 6AnimalsAutopsyBiomarkersBrainCaspase 12Cell HypoxiaCell SurvivalEndoplasmic ReticulumFemaleHumansHypoxia-Ischemia, BrainInfant, NewbornL-Lactate DehydrogenaseActivating Transcription Factor 6ATF6 protein, humanAtf6 protein, ratBiomarkersCASP12 protein, humanCasp12 protein, ratCaspase 12L-Lactate DehydrogenaseapoptosisATF6caspase-12ER stressneonatal hypoxic-ischemic encephalopathy

Identifiers

PMID26261584
PMCPMC4525918
OpenAlexW2415926178

What OpenQuestion holds

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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 OpenQuestion graph.