Evidence map›Paper›PMID 10435636›Full record

ArticleOncogene1999

Osteopontin induces increased invasiveness and plasminogen activator expression of human mammary epithelial cells.

A B Tuck, D M Arsenault, F P O'Malley, C Hota, M C Ling, S M Wilson, A F Chambers

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 188 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Kindlins as modulators of breast cancer progression.Journal of breast cancer research · 2021
    Article
  7. Mesenchymal Stromal Cells: Emerging Roles in Bone Metastasis.International journal of molecular sciences · 2018
    Review
  8. Article
  9. Article
  10. Pathogenesis of Warthin's tumors.Interventional medicine & applied science · 2016
    Review
  11. Review
  12. Article
  13. Role of osteopontin in the pathophysiology of cancer.Matrix biology : journal of the International Society for Matrix Biology · 2014
    Review
  14. Review
  15. Article
  16. Article
  17. miR-21 represses Pdcd4 during cardiac valvulogenesis.Development (Cambridge, England) · 2013
    Article
  18. Article
  19. Article
  20. Structure and function of the solid tumor niche.Frontiers in bioscience (Scholar edition) · 2012
    Review

13 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

A B TuckDepartment of Pathology, London Health Sciences Centre, University of Western Ontario, Canada.
D M Arsenault
F P O'Malley
C Hota
M C Ling
S M Wilson
A F Chambers
Ottawa Regional Cancer Foundation · CALondon Health Sciences Centre · CAWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopontin (OPN) has been associated with enhanced malignancy in breast cancer, but its functional role in this disease is poorly understood. To study the effect of OPN on cellular invasiveness, basal OPN expression was first assessed in members of a progression series of human mammary epithelial cell lines (21PT: immortalized, non-tumorigenic; 21NT: weakly tumorigenic; 21MT-1: tumorigenic, weakly metastatic; MDA-MB-435 cells: tumorigenic, highly metastatic). The two lines which expressed lowest basal levels of OPN (21PT, 21NT) were then examined for up-regulation of invasive behavior in response to exogenous or transfected (endogenous) OPN. Both 21PT and 21NT showed increased invasiveness through Matrigel when human recombinant (hr)OPN was added to the lower chamber of transwells. Both also showed a cell migration response to hrOPN. Populations of 21PT and 21NT cells stably transfected with an OPN-expression vector showed higher levels of cell invasiness than control vector transfectants. Examination of transfectants for mRNA of a number of secreted proteases showed that only urokinase-type plasminogen activator (uPA) expression was closely associated with OPN expression and cellular invasiveness. Treatment of the parental 21PT and 21NT cells with exogenous hrOPN resulted in increased uPA mRNA expression and increased urokinase activity of the conditioned media. Both increased cell migration and induction of uPA expression are thus potential mechanisms of increased invasiness of breast epithelial cells in response to OPN.

Indexed as

BreastBreast NeoplasmsCell Line, TransformedCell Transformation, NeoplasticCollagenCulture Media, ConditionedDisease ProgressionDrug CombinationsEpithelial CellsExtracellular MatrixFemaleGene Expression Regulation, NeoplasticHumansLamininNeoplasm InvasivenessNeoplasm MetastasisCollagenCulture Media, ConditionedDrug CombinationsLamininmatrigelNeoplasm ProteinsOsteopontinProteoglycansRecombinant Fusion ProteinsRNA, MessengerRNA, NeoplasmSialoglycoproteinsSPP1 protein, humanUrokinase-Type Plasminogen Activator

Identifiers

PMID10435636
OpenAlexW2319411522

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.