Evidence map›Paper›PMID 31741263›Full record

ArticleMolecular biology reports2020

Nesprin-1 impact on tumorigenic cell phenotypes.

Ilknur Sur-Erdem, Muhammed Sajid Hussain, Maria Asif, Nareg Pınarbası, Ali Cenk Aksu, Angelika A Noegel

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Emerin deficiency drives MCF7 cells to an invasive phenotype.bioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Oral Microbiota-Driven Cell Migration in Carcinogenesis and Metastasis.Frontiers in cellular and infection microbiology · 2022
    Review
  16. Biomedicines · 2021
    Article
  17. Review
  18. Article
  19. Review
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

6 authors.

Ilknur Sur-ErdemInstitute of Biochemistry I, Medical Faculty, University Hospital Cologne, Cologne, Germany. isur@ku.edu.tr.ORCID http://orcid.org/0000-0001-5035-4905
Muhammed Sajid HussainInstitute of Biochemistry I, Medical Faculty, University Hospital Cologne, Cologne, Germany.
Maria AsifInstitute of Biochemistry I, Medical Faculty, University Hospital Cologne, Cologne, Germany.
Nareg PınarbasıKoç University School of Medicine, 34450, Istanbul, Turkey.
Ali Cenk AksuKoç University School of Medicine, 34450, Istanbul, Turkey.
Angelika A NoegelInstitute of Biochemistry I, Medical Faculty, University Hospital Cologne, Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The largest protein of the nuclear envelope (NE) is Nesprin-1 which forms a network along the NE interacting with actin, Emerin, Lamin, and SUN proteins. Mutations in the SYNE1 gene and reduction in Nesprin-1 protein levels have been reported to correlate with several age related diseases and cancer. In the present study, we tested whether Nesprin-1 overexpression can reverse the malignant phenotype of Huh7 cells, a human liver cancer cell line, which carries a mutation in the SYNE1 gene resulting in reduced Nesprin-1 protein levels, has altered nuclear shape, altered amounts and localization of NE components, centrosome localization and genome stability. Ectopic expression of a mini-Nesprin-1 led to an improvement of the nuclear shape, corrected the mislocalization of NE proteins, the centrosome positioning, and the alterations in the DNA damage response network. Additionally, Nesprin-1 had a profound effect on cellular senescence. These findings suggest that Nesprin-1 may be effective in tumorigenic cell phenotype correction of human liver cancer.

Indexed as

ActinsCarcinogenesisCell Line, TumorCell NucleusCytoskeletal ProteinsGene ExpressionGene Expression Regulation, NeoplasticHumansMicrofilament ProteinsNerve Tissue ProteinsNuclear EnvelopePhenotypeActinsCytoskeletal ProteinsMicrofilament ProteinsNerve Tissue ProteinsSYNE1 protein, humanCancerCellular senescenceGenome stabilityNesprin-1Nuclear envelope

Identifiers

What OpenQuestion holds

Textmetadata
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.