Evidence map›Paper›PMID 23933250›Full record

ArticleBiochemical and biophysical research communications2013

Fetuin-A (α2HS-glycoprotein) is a serum chemo-attractant that also promotes invasion of tumor cells through Matrigel.

Gladys N Nangami, Kurt Watson, Kitani Parker-Johnson, Kelechi O Okereke, Amos Sakwe, Pamela Thompson, Nanna Frimpong, Josiah Ochieng

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
0.6field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
    Pooled it
  2. Pooled it
  3. Antitumor effects of a lectin purified fromFrontiers in oncology · 2026
    Article
  4. Article
  5. The Role of Fetuin-A in Tumor Cell Growth, Prognosis, and Dissemination.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Impact of Fetuin-A (AHSG) on Tumor Progression and Type 2 Diabetes.International journal of molecular sciences · 2018
    Review
  18. Usefulness of serum fetuin-A level as a marker of erectile dysfunction.International journal of impotence research · 2017
    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

8 authors at 2 institutions in 1 country.

Gladys N NangamiDepartment of Biochemistry and Cancer Biology, Meharry Medical College, Nashville, TN 37208, United States.
Kurt Watson
Kitani Parker-Johnson
Kelechi O Okereke
Amos Sakwe
Pamela Thompson
Nanna Frimpong
Josiah Ochieng
Meharry Medical College · USXavier University of Louisiana · US

Funding

Understanding and Controlling p120 Dysfunction in CRCP50CA095103 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2002 to 2017
$33.6M
Translational Pathology CoreU54CA163069 · NCI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 2011 to 2025
$18.8M
TECHNOLOGIES AND RESOURCES FOR CORE LABORATORIESU54RR026140 · NCRR · MEHARRY MEDICAL COLLEGE · PI GOODWIN, JEFFREY SHAWN · 2009 to 2011
$12.9M
Meharry RCMI Program in Women's Health ResearchG12MD007586 · NIMHD · MEHARRY MEDICAL COLLEGE · PI HILDRETH, JAMES E · 2012 to 2016
$7.8M
Minority Institution Research Training ProgramT32HL007735 · NHLBI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 1992 to 2014
$2.9M
Role of Fetuin-A in Tumor Cell GrowthSC1CA134018 · NCI · MEHARRY MEDICAL COLLEGE · PI OCHIENG, JOSIAH · 2007 to 2012
$1.7M
NCI NIH HHS 3SC1CA134018-04S1NCI NIH HHS P50 CA095103NCI NIH HHS SC1 CA134018NCI NIH HHS U54 CA163069NCRR NIH HHS U54 RR026140NHLBI NIH HHS 5 T32 HL007735-15NHLBI NIH HHS T32 HL007735NIMHD NIH HHS G12 MD007586
6 · The paper itself

Abstract

The present study was conducted to determine whether fetuin-A, a dominant serum protein plays a role in chemo-attraction and chemo-invasion of carcinoma cells in vitro. Serum is normally used as positive chemotaxis control in Boyden chamber motility assays, prompting the need to identify the factor/s in serum that contributes the bulk of chemo-taxis and invasion. Serum has a plethora of chemotactic factors including stromal derived factor 1 also known as CXCL12. Using highly purified fetuin-A, we compared its chemo-attraction potential to culture medium containing 10% fetal bovine serum. We also investigated its ability to attract tumor cells through a bed of Matrigel (invasion assay). We demonstrated, using similar concentration range of fetuin-A found in blood, that it robustly supports both directed chemo-attraction and invasion of breast tumor cells. More importantly, we showed that at low concentrations (fetuin-A coated wells) itinteracts synergistically with CXCL12 to promote chemotaxis. The presence of plasminogen (PL) blunted the fetuin-A mediated chemotaxis. Taken together, the data suggest an in vivo chemotaxis/invasion role for fetuin-A.

Indexed as

Chemotaxisalpha-2-HS-GlycoproteinAnimalsBiocompatible MaterialsBreastBreast NeoplasmsCattleCell Line, TumorChemokine CXCL12CollagenColonColonic NeoplasmsDrug CombinationsFemaleHumansLamininalpha-2-HS-GlycoproteinBiocompatible MaterialsChemokine CXCL12CollagenDrug CombinationsLamininmatrigelPlasminogenProteoglycansChemo-attractionChemo-invasionChemotaxisExosomesFetuin-AGradient

Identifiers

PMID23933250
PMCPMC3833465
OpenAlexW2045180212

What OpenQuestion holds

Textmetadata
LicenceTDM
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.