Evidence map›Paper›PMID 33604728›Full record

ReviewApoptosis : an international journal on programmed cell death2021

Role of apoptosis repressor with caspase recruitment domain (ARC) in cell death and cardiovascular disease.

Jing Zhang, Xianxin Zheng, Peiyan Wang, Jianxun Wang, Wei Ding

Abstract readReview
PubMed Publisher
In one paragraph

Review in Apoptosis : an international journal on programmed cell death, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Cell death in atherosclerosis.Cell cycle (Georgetown, Tex.) · 2024
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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.

Jing ZhangDepartment of Comprehensive Internal Medicine, Affiliated Hospital, Qingdao University, Qingdao, 266000, China.
Xianxin ZhengSchool of Basic Medical Sciences, Qingdao University, Qingdao, China.
Peiyan WangSchool of Basic Medical Sciences, Qingdao University, Qingdao, China.
Jianxun WangSchool of Basic Medical Sciences, Qingdao University, Qingdao, China. wangjx@qdu.edu.cn.
Wei DingDepartment of Comprehensive Internal Medicine, Affiliated Hospital, Qingdao University, Qingdao, 266000, China. dingwei@qdu.edu.cn.ORCID http://orcid.org/0000-0003-3564-970X
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis repressor with caspase recruitment domain (ARC) is a highly effective and multifunctional inhibitor of apoptosis that is mainly expressed in postmitotic cells such as cardiomyocytes and skeletal muscle cells. ARC contains a C-terminal region rich in proline and glutamic acid residues and an N-terminal caspase recruitment domain (CARD). The CARD is originally described as a protein-binding motif that interacts with caspase through a CARD-CARD interaction. Initially, the inhibitory effect of ARC was only found in apoptosis, however, it was later found that ARC also played a regulatory role in other types of cell death. As a powerful cardioprotective factor, ARC can protect the heart by inhibiting the death of cardiomyocytes in various ways. ARC can reduce the cardiomyocyte apoptotic response to various stresses and injuries, including extrinsic apoptosis induced by death receptor ligands, cellular Ca

Indexed as

ApoptosisCaspase Activation and Recruitment DomainAnimalsCalciumCardiovascular DiseasesCaspasesCell DeathEndoplasmic Reticulum StressHumansOxidative StressCalciumCaspasesApoptosis repressor with caspase recruitment domain (ARC)CardiomyocyteCardiovascular diseaseCell death

Identifiers

PMID33604728
OpenAlexW3131387804

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.