Evidence map›Paper›PMID 36291930›Full record

ArticleCancers2022

Role of N-Cadherin in Epithelial-to-Mesenchymal Transition and Chemosensitivity of Colon Carcinoma Cells.

Veronika Skarkova, Barbora Vitovcova, Petra Matouskova, Monika Manethova, Petra Kazimirova, Adam Skarka, Veronika Brynychova, Pavel Soucek, Hana Vosmikova, Emil Rudolf

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

10 authors at 2 institutions in 1 country.

Veronika SkarkovaDepartment of Medical Biology and Genetics, Faculty of Medicine in Hradec Kralove, Charles University, Zborovska 2089, 500 03 Hradec Kralove, Czech Republic.
Barbora VitovcovaDepartment of Medical Biology and Genetics, Faculty of Medicine in Hradec Kralove, Charles University, Zborovska 2089, 500 03 Hradec Kralove, Czech Republic.
Petra MatouskovaDepartment of Biochemistry, Faculty of Pharmacy, Charles University, Akademika Heyrovskeho 1203, 500 05 Hradec Kralove, Czech Republic.ORCID 0000-0002-9421-5744
Monika ManethovaThe Fingerland Department of Pathology, Faculty of Medicine, University Hospital in Hradec Kralove, Charles University, Sokolska 581, 500 05 Hradec Kralove, Czech Republic.ORCID 0000-0003-0083-3283
Petra KazimirovaDepartment of Medical Biochemistry, Faculty of Medicine in Hradec Kralove, Charles University, Zborovska 2089, 500 03 Hradec Kralove, Czech Republic.
Adam SkarkaDepartment of Chemistry, Faculty of Sciences, University of Hradec Kralove, Hradecká 1285, 500 03 Hradec Kralove, Czech Republic.
Veronika BrynychovaDepartment of Toxicogenomics, National Institute of Public Health, Srobarova 49/48, 100 00 Prague, Czech Republic.
Pavel SoucekDepartment of Toxicogenomics, National Institute of Public Health, Srobarova 49/48, 100 00 Prague, Czech Republic.ORCID 0000-0002-4294-6799
Hana VosmikovaThe Fingerland Department of Pathology, Faculty of Medicine, University Hospital in Hradec Kralove, Charles University, Sokolska 581, 500 05 Hradec Kralove, Czech Republic.
Emil RudolfDepartment of Medical Biology and Genetics, Faculty of Medicine in Hradec Kralove, Charles University, Zborovska 2089, 500 03 Hradec Kralove, Czech Republic.ORCID 0000-0002-9526-3174
Charles University · CZUniversity of Hradec Králové · CZ

Funding

Charles University Cooperatio, DIAGCzech Medical Council NV19 08 00113
6 · The paper itself

Abstract

(1) Background: N-cadherin expression, epithelial-to-mesenchymal transition (EMT) and aggressive biological phenotype of tumor cells are linked although the underlying mechanisms are not entirely clear. (2) Methods: In this study, we used two different in vitro cell models with varying N-cadherin expression (stabilized lines and primocultures) and investigated their select biological features including the degree of their chemoresistance both in vitro as well as in vivo. (3) Results: We report that although enforced N-cadherin expression changes select morphological and behavioral characteristics of exposed cells, it fails to successfully reprogram cells to the aggressive, chemoresistant phenotype both in vitro as well as in vivo as verified by implantation of those cells into athymic mice. Conversely, primocultures of patient-colonic cells with naturally high levels of N-cadherin expression show fully aggressive and chemoresistant phenotype pertinent to EMT (in vitro and in vivo), with a potential to develop new mutations and in the presence of dysregulated regulatory pathways as represented by investigated miRNA profiles. (4) Conclusions: The presented results bring new facts concerning the functional axis of N-cadherin expression and related biological features of colon cancer cells and highlight colon cancer primocultures as a useful model for such studies.

Indexed as

chemosensitivitycolon cancerEMTmiRNAN-cadherinprimocultures

Identifiers

PMID36291930
PMCPMC9601123
OpenAlexW4306920743

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.