Evidence map›Paper›PMID 35178230›Full record

ArticleJournal of healthcare engineering2022

Inhibiting Autophagy Pathway of PI3K/AKT/mTOR Promotes Apoptosis in SK-N-SH Cell Model of Alzheimer's Disease.

Yu Pang, Wennan Lin, Lan Zhan, Jiawen Zhang, Shicun Zhang, Hongwei Jin, He Zhang, Xiaoli Wang, Xiaoming Li

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Journal of healthcare engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Yu PangDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0003-4938-516X
Wennan LinGeneral Department, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-3932-4809
Lan ZhanDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0003-0169-9119
Jiawen ZhangDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-8595-3403
Shicun ZhangDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-9355-6475
Hongwei JinDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-7509-2697
He ZhangDepartment of Neurology, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-9540-8935
Xiaoli WangSchool of Pharmacy, Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0002-4625-807X
Xiaoming LiThe Institute of Medicine, Qiqihar Medical University, Qiqihar 161000, China.ORCID 0000-0001-6533-2872
Qiqihar Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease is the most common dementia disease characterized by chronic progressive neurodegeneration. The incidence of Alzheimer's disease is on the rise as the population ages at an accelerating pace. According to epidemiological data, by 2050, the number of Alzheimer's patients in the United States will be three times higher than that in 2010, and a similar trend is occurring in China. To explore the effect and mechanism of let-7b by detecting the expression level of let-7b in Alzheimer's disease, fifty patients with Alzheimer's disease and thirty healthy controls were selected. The expression levels of let-7 families (let-7a, let-7b, let-7c, let-7d, let-7e, let-7f, let-7g, and let-7i) were detected by qPCR. Human neuroblastoma cell SK-N-SH were divided into control group (untreated), model group (treated with A

Indexed as

Alzheimer DiseaseMicroRNAsApoptosisAutophagyBeclin-1Caspase 3HumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesBeclin-1Caspase 3MicroRNAsMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID35178230
PMCPMC8846974
OpenAlexW4210880559

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.