Evidence map›Paper›PMID 37353408›Full record

ReviewTrends in molecular medicine2023

Pushing the boundaries of brain organoids to study Alzheimer's disease.

Jonas Cerneckis, Guojun Bu, Yanhong Shi

Open access · hybridAbstract readReview
In one paragraph

Review in Trends in molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Human iPSC models revealResearch square · 2026
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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

3 authors at 2 institutions in 1 country.

Jonas CerneckisDepartment of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA; Irell and Manella Graduate School of Biological Sciences, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.
Guojun BuSciNeuro Pharmaceuticals, Rockville, MD 20850, USA.
Yanhong ShiDepartment of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA; Irell and Manella Graduate School of Biological Sciences, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA. Electronic address: yshi@coh.org.
Beckman Research InstituteCity of Hope · US

Funding

ApoE2 in Alzheimer's disease: the neuroprotective effects and mechanismsRF1AG061794 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SHI, YANHONG · 2018 to 2018
$3.1M
Modeling Alzheimer’s disease using directly reprogrammed isogenic neural cellsR01AG056305 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI HUANG, YADONG, SHI, YANHONG · 2017 to 2021
$2.2M
Develop age-relevant glial cellular models using human directly reprogrammed cellsR01AG072291 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SHI, YANHONG · 2021 to 2025
$2.2M
Define the effect of CLU SNP on the risk to Alzheimer's diseaseRF1AG079307 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SHI, YANHONG · 2022 to 2022
$1.9M
NIA NIH HHS R01 AG056305NIA NIH HHS R01 AG072291NIA NIH HHS RF1 AG061794NIA NIH HHS RF1 AG079307
6 · The paper itself

Abstract

Progression of Alzheimer's disease (AD) entails deterioration or aberrant function of multiple brain cell types, eventually leading to neurodegeneration and cognitive decline. Defining how complex cell-cell interactions become dysregulated in AD requires novel human cell-based in vitro platforms that could recapitulate the intricate cytoarchitecture and cell diversity of the human brain. Brain organoids (BOs) are 3D self-organizing tissues that partially resemble the human brain architecture and can recapitulate AD-relevant pathology. In this review, we highlight the versatile applications of different types of BOs to model AD pathogenesis, including amyloid-β and tau aggregation, neuroinflammation, myelin breakdown, vascular dysfunction, and other phenotypes, as well as to accelerate therapeutic development for AD.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBrainHumansOrganoidsPhenotypeAmyloid beta-PeptidesAlzheimer’s diseaseApolipoprotein E4brain organoidsdrug discoveryinduced pluripotent stem cellsmyelin organoids

Identifiers

PMID37353408
PMCPMC10374393
OpenAlexW4381550217

What OpenQuestion holds

Textmetadata
LicenceTDM
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.