Evidence map›Paper›PMID 33327559›Full record

ArticleInternational journal of molecular sciences2020

Alzheimer's, Parkinson's Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement.

Maria Garofalo, Cecilia Pandini, Matteo Bordoni, Orietta Pansarasa, Federica Rey, Alfredo Costa, Brigida Minafra, Luca Diamanti, Susanna Zucca, Stephana Carelli and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 46 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 4 institutions in 1 country.

Maria GarofaloGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Cecilia PandiniGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Matteo BordoniDipartimento di Scienze Farmacologiche e Biomolecolari (DiSFeB), Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, Via Balzaretti 9, 20133 Milano, Italy.
Orietta PansarasaGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-3041-0612
Federica ReyDepartment of Biomedical and Clinical Sciences "Luigi Sacco", University of Milan, Via G.B Grassi 74, 20157 Milan, Italy.ORCID 0000-0001-7944-3143
Alfredo CostaUnit of Behavioral Neurology, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Brigida MinafraParkinson Unit and Movement disorders Mondino Foundation IRCCS, 27100 Pavia, Italy.
Luca DiamantiNeuro-Oncology Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Susanna ZuccaGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Stephana CarelliDepartment of Biomedical and Clinical Sciences "Luigi Sacco", University of Milan, Via G.B Grassi 74, 20157 Milan, Italy.ORCID 0000-0003-4603-396X
Cristina CeredaGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Stella GagliardiGenomic and Post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-6589-6907
Italian institute for Genomic Medicine · ITUniversity of Milan · ITUniversity of Pavia · ITFondazione Istituto Neurologico Nazionale Casimiro Mondino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS) are neurodegenerative disorders characterized by a progressive degeneration of the central or peripheral nervous systems. A central role of the RNA metabolism has emerged in these diseases, concerning mRNAs processing and non-coding RNAs biogenesis. We aimed to identify possible common grounds or differences in the dysregulated pathways of AD, PD, and ALS. To do so, we performed RNA-seq analysis to investigate the deregulation of both coding and long non-coding RNAs (lncRNAs) in ALS, AD, and PD patients and controls (CTRL) in peripheral blood mononuclear cells (PBMCs). A total of 293 differentially expressed (DE) lncRNAs and 87 mRNAs were found in ALS patients. In AD patients a total of 23 DE genes emerged, 19 protein coding genes and four lncRNAs. Through Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) analyses, we found common affected pathways and biological processes in ALS and AD. In PD patients only five genes were found to be DE. Our data brought to light the importance of lncRNAs and mRNAs regulation in three principal neurodegenerative disorders, offering starting points for new investigations on deregulated pathogenic mechanisms.

Indexed as

Alzheimer DiseaseAmyotrophic Lateral SclerosisHumansParkinson DiseaseRNA, Long NoncodingRNA, MessengerRNA-SeqRNA, Long NoncodingRNA, MessengerAlzheimer’s diseaseamyotrophic lateral sclerosisgene expressionlong non-coding RNAsParkinson’s disease

Identifiers

PMID33327559
PMCPMC7765024
OpenAlexW3112043183

What OpenQuestion holds

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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.