Evidence map›Paper›PMID 28616035›Full record

ArticleNeural regeneration research2017

Neuroprotective effects of Activin A on endoplasmic reticulum stress-mediated apoptotic and autophagic PC12 cell death.

Long-Xing Xue, Hong-Yu Liu, Yang Cui, Yue Dong, Jiao-Qi Wang, Qiu-Ye Ji, Jin-Ting He, Min Yao, Ying-Ying Wang, Yan-Kun Shao and 2 more

Open access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Long-Xing XueDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Hong-Yu LiuDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Yang CuiDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Yue DongDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Jiao-Qi WangDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Qiu-Ye JiResearch Center, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Jin-Ting HeDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Min YaoDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Ying-Ying WangDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Yan-Kun ShaoDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.
Jing MangDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.ORCID 0000-0003-3154-9218
Zhong-Xin XuDepartment of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin Province, China.ORCID 0000-0001-7066-7159
Jilin University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activin A, a member of the transforming growth factor-beta superfamily, plays a neuroprotective role in multiple neurological diseases. Endoplasmic reticulum (ER) stress-mediated apoptotic and autophagic cell death is implicated in a wide range of diseases, including cerebral ischemia and neurodegenerative diseases. Thapsigargin was used to induce PC12 cell death, and Activin A was used for intervention. Our results showed that Activin A significantly inhibited morphological changes in thapsigargin-induced apoptotic cells, and the expression of apoptosis-associated proteins [cleaved-caspase-12, C/EBP homologous protein (CHOP) and cleaved-caspase-3] and biomarkers of autophagy (Beclin-1 and light chain 3), and downregulated the expression of thapsigargin-induced ER stress-associated proteins [inositol requiring enzyme-1 (IRE1), tumor necrosis factor receptor-associated factor 2 (TRAF2), apoptosis signal-regulating kinase 1 (ASK1), c-Jun N-terminal kinase (JNK) and p38]. The inhibition of thapsigargin-induced cell death was concentration-dependent. These findings suggest that administration of Activin A protects PC12 cells against ER stress-mediated apoptotic and autophagic cell death by inhibiting the activation of the IRE1-TRAF2-ASK1-JNK/p38 cascade.

Indexed as

Activin Aapoptosisautophagyc-Jun N-terminal kinaseendoplasmic reticulum stressnerve regenerationneural regenerationp38

Identifiers

PMID28616035
PMCPMC5461616
OpenAlexW2617377847

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.