Evidence map›Paper›PMID 34589606›Full record

ArticleBioengineering & translational medicine2021

E3 ligase activity of Carboxyl terminus of Hsc70 interacting protein (CHIP) in Wharton's jelly derived mesenchymal stem cells improves their persistence under hyperglycemic stress and promotes the prophylactic effects against diabetic cardiac damages.

Ayaz Ali, Wei-Wen Kuo, Chia-Hua Kuo, Jeng-Fan Lo, Michael Y C Chen, Jayasimha R Daddam, Tsung-Jung Ho, Vijaya Padma Viswanadha, Marthandam Asokan Shibu, Chih-Yang Huang

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-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

9 citing papers in PubMed, 24 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

10 authors at 8 institutions in 2 countries.

Ayaz AliDepartment of Biological Science and Technology China Medical University Taichung Taiwan.
Wei-Wen KuoDepartment of Biological Science and Technology China Medical University Taichung Taiwan.
Chia-Hua KuoLaboratory of Exercise Biochemistry University of Taipei Taipei Taiwan.
Jeng-Fan LoInstitute of Oral Biology, National Yang-Ming University Taipei Taiwan.
Michael Y C ChenDepartment of Cardiology Buddhist Tzu Chi General Hospital Hualien Taiwan.
Jayasimha R DaddamCardiovascular and Mitochondrial Related Disease Research Center, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation Hualien Taiwan.
Tsung-Jung HoDepartment of Chinese Medicine Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Tzu Chi University Hualien Taiwan.
Vijaya Padma ViswanadhaDepartment of Biotechnology Bharathiar University Coimbatore India.
Marthandam Asokan ShibuCardiovascular and Mitochondrial Related Disease Research Center, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation Hualien Taiwan.ORCID https://orcid.org/0000-0001-6381-3525
Chih-Yang HuangCardiovascular and Mitochondrial Related Disease Research Center, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation Hualien Taiwan.ORCID https://orcid.org/0000-0003-2347-0411
China Medical University · TWTzu Chi Foundation · TWAsia University · TWBharathiar University · INBuddhist Tzu Chi General Hospital · TWNational Yang Ming Chiao Tung University · TWTzu Chi University · TWUniversity of Taipei · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies indicate that umbilical cord stem cells are cytoprotective against several disorders. One critical limitation in using stem cells is reduction in their viability under stressful conditions, such as diabetes. However, the molecular intricacies responsible for diabetic conditions are not fully elucidated. In this study, we found that high glucose (HG) conditions induced loss of chaperone homeostasis, stabilized PTEN, triggered the downstream signaling cascade, and induced apoptosis and oxidative stress in Wharton's jelly derived mesenchymal stem cells (WJMSCs). Increased Carboxyl terminus of Hsc70 interacting protein (CHIP) expression promoted phosphatase and tensin homolog (PTEN) degradation via the ubiquitin-proteasome system and shortened its half-life during HG stress. Docking studies confirmed the interaction of CHIP with PTEN and FOXO3a with the

Indexed as

apoptosiscarboxyl terminus of Hsc70 interacting proteindiabetesphosphatase and tensin homologWharton's jelly derived mesenchymal stem cells

Identifiers

PMID34589606
PMCPMC8459600
OpenAlexW3165815823

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.