Evidence map›Paper›PMID 24586201›Full record

SynthesisPLoS genetics2014

Molecular evidence for the inverse comorbidity between central nervous system disorders and cancers detected by transcriptomic meta-analyses.

Kristina Ibáñez, César Boullosa, Rafael Tabarés-Seisdedos, Anaïs Baudot, Alfonso Valencia

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 3 pooled it
13.8field-weighted citation impact, top 1% 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

117 citing papers in PubMed, 3 syntheses or guidelines pooled it, 210 citations in OpenAlex.

  1. Pooled it
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  3. Inverse relationship between cancer and Alzheimer's disease: a systemic review meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2015
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  10. Patient stratification reveals the molecular basis of disease co-occurrences.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  20. Implications of TDP-43 in non-neuronal systems.Cell communication and signaling : CCS · 2023
    Review

57 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 3 countries.

Kristina IbáñezStructural Biology and Biocomputing Programme, Spanish National Cancer, Research Centre (CNIO), Madrid, Spain.
César BoullosaStructural Biology and Biocomputing Programme, Spanish National Cancer, Research Centre (CNIO), Madrid, Spain.
Rafael Tabarés-SeisdedosDepartment of Medicine, University of Valencia, CIBERSAM, INCLIVA, Valencia, Spain.
Anaïs BaudotAix-Marseille Université, CNRS, I2M, UMR 7373, Marseille, France.
Alfonso ValenciaStructural Biology and Biocomputing Programme, Spanish National Cancer, Research Centre (CNIO), Madrid, Spain.
Spanish National Cancer Research Centre · ESCentre National de la Recherche Scientifique · FRCentro de Investigación del Cáncer · ESINCLIVA Health Research Institute · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is epidemiological evidence that patients with certain Central Nervous System (CNS) disorders have a lower than expected probability of developing some types of Cancer. We tested here the hypothesis that this inverse comorbidity is driven by molecular processes common to CNS disorders and Cancers, and that are deregulated in opposite directions. We conducted transcriptomic meta-analyses of three CNS disorders (Alzheimer's disease, Parkinson's disease and Schizophrenia) and three Cancer types (Lung, Prostate, Colorectal) previously described with inverse comorbidities. A significant overlap was observed between the genes upregulated in CNS disorders and downregulated in Cancers, as well as between the genes downregulated in CNS disorders and upregulated in Cancers. We also observed expression deregulations in opposite directions at the level of pathways. Our analysis points to specific genes and pathways, the upregulation of which could increase the incidence of CNS disorders and simultaneously lower the risk of developing Cancer, while the downregulation of another set of genes and pathways could contribute to a decrease in the incidence of CNS disorders while increasing the Cancer risk. These results reinforce the previously proposed involvement of the PIN1 gene, Wnt and P53 pathways, and reveal potential new candidates, in particular related with protein degradation processes.

Indexed as

ComorbidityAlzheimer DiseaseCentral Nervous SystemGene Expression ProfilingGene Expression RegulationHumansNeoplasmsNIMA-Interacting Peptidylprolyl IsomeraseParkinson DiseasePeptidylprolyl IsomeraseSchizophreniaSignal TransductionNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePIN1 protein, human

Identifiers

PMID24586201
PMCPMC3930576
OpenAlexW2006382458

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.