Evidence map›Paper›PMID 32756405›Full record

ArticleCells2020

Overexpression of Extradomain-B Fibronectin is Associated with Invasion of Breast Cancer Cells.

Amita Vaidya, Helen Wang, Victoria Qian, Hannah Gilmore, Zheng-Rong Lu

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Vasculature organotropism in drug delivery.Advanced drug delivery reviews · 2023
    Review
  17. Review
  18. Article
  19. Article
  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

5 authors at 2 institutions in 1 country.

Amita VaidyaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Helen WangDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Victoria QianDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.ORCID 0000-0001-9711-5290
Hannah GilmoreDepartment of Pathology, University Hospitals of Cleveland, Cleveland, OH 44106, USA.
Zheng-Rong LuDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Case Western Reserve University · USUniversity Hospitals of Cleveland · US

Funding

Smart nanoparticles regulating oncogenic IncRNA for breast cancer therapyR01CA235152 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI ZHENG-RONG LU, William Schiemann · 2019 to 2026
$3.2M
Image-guided EMT inhibition for treating metastatic breast cancerR01CA194518 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LU, ZHENG-RONG, SCHIEMANN, WILLIAM · 2015 to 2019
$2.4M
Targeted MRI contrast agents for differential diagnosis of prostate cancerR01CA211762 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LU, ZHENG-RONG · 2017 to 2021
$2.1M
NCI NIH HHS R01 CA194518NCI NIH HHS R01 CA211762NCI NIH HHS R01 CA235152
6 · The paper itself

Abstract

Breast tumor heterogeneity is a major impediment to oncotherapy. Cancer cells undergo rapid clonal evolution, thereby acquiring significant growth and invasive advantages. The absence of specific markers of these high-risk populations precludes efficient therapeutic and diagnostic management of the disease. Given the critical function of tumor microenvironment in the oncogenic circuitry, we sought to determine the expression profile of the extracellular matrix oncoprotein, extradomain-B fibronectin (EDB-FN) in invasive breast cancer. Analyses of TCGA/GTEx databases and immunostaining of clinical samples found a significant overexpression of EDB-FN in breast tumors, which correlated with poor overall survival. Significant upregulation of EDB-FN was observed in invasive cell populations generated from relatively less invasive MCF7 and MDA-MB-468 cells by long-term TGF-β treatment and acquired chemoresistance. Treatment of the invasive cell populations with an AKT inhibitor (MK2206-HCl) reduced their invasive potential, with a concomitant decrease in their EDB-FN expression, partly through the phosphoAKT-SRp55 pathway. EDB-FN downregulation, with direct RNAi of EDB-FN or indirectly through RNAi of SRp55, also resulted in reduced motility of the invasive cell populations, validating the correlation between EDB-FN expression and invasion of breast cancer cells. These data establish EDB-FN as a promising molecular marker for non-invasive therapeutic surveillance of aggressive breast cancer.

Indexed as

Breast NeoplasmsCell Line, TumorDrug Resistance, NeoplasmFemaleFibronectinsGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessPhosphoproteinsProto-Oncogene Proteins c-aktSerine-Arginine Splicing FactorsTransforming Growth Factor betaTumor MicroenvironmentFibronectinsFN1 protein, humanPhosphoproteinsProto-Oncogene Proteins c-aktSerine-Arginine Splicing FactorsSRSF6 protein, humanTransforming Growth Factor betabreast cancerdrug resistanceEDB-FNinvasionTGF-βtumor microenvironment

Identifiers

PMID32756405
PMCPMC7463489
OpenAlexW3046626762

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.