Evidence map›Paper›PMID 30845770›Full record

ArticleCancers2019

Insight into the Role and Regulation of Gap Junction Genes in Lung Cancer and Identification of Nuclear Cx43 as a Putative Biomarker of Poor Prognosis.

Trond Aasen, Irene Sansano, Maria Ángeles Montero, Cleofé Romagosa, Jordi Temprana-Salvador, Alexandre Martínez-Marti, Teresa Moliné, Javier Hernández-Losa, Santiago Ramón y Cajal

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Mutations of theMedicina (Kaunas, Lithuania) · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Identification and Verification of mFrontiers in immunology · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. The mutual interplay of redox signaling and connexins.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. Observational
  20. Article
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

9 authors at 2 institutions in 1 country.

Trond AasenTranslational Molecular Pathology, Vall d'Hebron Research Institute (VHIR), Barcelona 08035, Spain. trond.aasen@vhir.org.
Irene SansanoPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. isansava@gmail.com.
Maria Ángeles MonteroPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. angeles.montero@mft.nhs.uk.
Cleofé RomagosaPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. cleoferoma@gmail.com.
Jordi Temprana-SalvadorPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. jordi.temprana@gmail.com.
Alexandre Martínez-MartiMedical Oncology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. alexmartinezmarti.oncologia@gmail.com.
Teresa MolinéPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. teresa.moline@vhir.org.
Javier Hernández-LosaPathology Department, Vall d'Hebron University Hospital, Barcelona 08035, Spain. jahernan@vhebron.net.
Santiago Ramón y CajalTranslational Molecular Pathology, Vall d'Hebron Research Institute (VHIR), Barcelona 08035, Spain. sramon@vhebron.net.
Vall d'Hebron Hospital Universitari · ESVall d'Hebron Institut de Recerca · ES

Funding

Instituto de Salud Carlos III CPII16/00042Instituto de Salud Carlos III PI13/00763Instituto de Salud Carlos III PI16/00772
6 · The paper itself

Abstract

Direct intercellular communication, mediated by gap junctions formed by the connexin transmembrane protein family, is frequently dysregulated in cancer. Connexins have been described as tumour suppressors, but emerging evidence suggests that they can also act as tumour promoters. This feature is connexin- and tissue-specific and may be mediated by complex signalling pathways through gap junctions or hemichannels or by completely junction-independent events. Lung cancer is the number one cancer in terms of mortality worldwide, and novel biomarkers and therapeutic targets are urgently needed. Our objective was to gain a better understanding of connexins in this setting. We used several in silico tools to analyse TCGA data in order to compare connexin mRNA expression between healthy lung tissue and lung tumours and correlated these results with gene methylation patterns. Using Kaplan-Meier plotter tools, we analysed a microarray dataset and an RNA-seq dataset of non-small cell lung tumours in order to correlate connexin expression with patient prognosis. We found that connexin mRNA expression is frequently either upregulated or downregulated in lung tumours. This correlated with both good and poor prognosis (overall survival) in a clear connexin isoform-dependent manner. These associations were strongly influenced by the histological subtype (adenocarcinoma versus squamous cell carcinoma). We present an overview of all connexins but particularly focus on four isoforms implicated in lung cancer: Cx26, Cx30.3, Cx32 and Cx43. We further analysed the protein expression and localization of Cx43 in a series of 73 human lung tumours. We identified a subset of tumours that exhibited a unique strong nuclear Cx43 expression pattern that predicted worse overall survival (

Indexed as

connexinsCx43gap junctionsimmunohistochemistrylung cancernuclearprognosis

Identifiers

PMID30845770
PMCPMC6468764
OpenAlexW2918620495

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.