Evidence map›Paper›PMID 35035682›Full record

ArticleAmerican journal of translational research2021

Curcumin slows the progression of Alzheimer's disease by modulating mitochondrial stress responses via JMJD3-H3K27me3-BDNF axis.

Jingna Li, Shanshan Wang, Simiao Zhang, Dan Cheng, Xiaopeng Yang, Yutong Wang, Honglei Yin, Yajun Liu, Yanqiu Liu, Hongying Bai and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 40% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 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 3 institutions in 1 country.

Jingna LiDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Shanshan WangDepartment of Neurology, 960 Hospital of PLA Zibo 255300, Shandong, China.
Simiao ZhangDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Dan ChengDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Xiaopeng YangDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Yutong WangQilu Medical College Zibo 255300, Shandong, China.
Honglei YinDepartment of Neurology, 960 Hospital of PLA Zibo 255300, Shandong, China.
Yajun LiuDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Yanqiu LiuDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Hongying BaiDepartment of Neurology, 960 Hospital of PLA Zibo 255300, Shandong, China.
Shuang GengDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Yunliang WangDepartment of Neurology, Second Affiliated Hospital of Zhengzhou University Zhengzhou 450014, Henan, China.
Second Affiliated Hospital of Zhengzhou University · CNQilu University of Technology · CNCentral Hospital of Zibo · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disturbance of mitochondrial proteins by amyloid beta-protein (Aβ) that associates with mitochondrial stress responses (MSR) is one of the pathological mechanisms of Alzheimer's disease (AD). This study tried to explore whether the axis of Jumonji domain-containing protein 3 (JMJD3)-trimethylated lysine 27 on histone H3 (H3K27me3)-brain derived neurotrophic factor (BDNF) is involved in the regulation of MSR which in turn intervenes in the process of AD, and whether curcumin (CUR) has a protective role against AD by influencing this axis, aiming to provide insights into AD treatment. AD mouse models presented a significant aggregation of Aβ, with conspicuous pathological changes in brain tissues and an increase in neuronal apoptosis. Moreover, the mRNA and protein levels of JMJD3 and BDNF were down-regulated, H3K27me3 methylation levels were increased, and the MSR markers (ClpP, HSP6, HSP-60, and ATFS-1) showed abnormal alterations. In

Indexed as

Alzheimer’s diseaseBDNFCurcuminH3K27me3JMJD3

Identifiers

PMID35035682
PMCPMC8748089
OpenAlexW4206870258

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.