Evidence map›Paper›PMID 16816376›Full record

ArticleThe American journal of pathology2006

Role of the integrin-binding protein osteopontin in lymphatic metastasis of breast cancer.

Alison L Allan, Rosamma George, Sharon A Vantyghem, Mark W Lee, Nicole C Hodgson, C Jay Engel, Ron L Holliday, David P Girvan, Leslie A Scott, Carl O Postenka and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Human osteopontin: Potential clinical applications in cancer (Review).International journal of molecular medicine · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. OPN -Revisited.Journal of clinical and diagnostic research : JCDR · 2015
    Review
  17. Article
  18. Article
  19. Role of osteopontin in the pathophysiology of cancer.Matrix biology : journal of the International Society for Matrix Biology · 2014
    Review
  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

15 authors at 3 institutions in 2 countries.

Alison L AllanDepartment of Oncology, Schulich School of Medicine and Dentistry, University of Western Ontario, London Regional Cancer Program, 790 Commissioners Road East, London, Ontario N6A 4L6, Canada. alison.allan@lhsc.on.ca
Rosamma George
Sharon A Vantyghem
Mark W Lee
Nicole C Hodgson
C Jay Engel
Ron L Holliday
David P Girvan
Leslie A Scott
Carl O Postenka
Waleed Al-Katib
Larry W Stitt
Toshimitsu Uede
Ann F Chambers
Alan B Tuck
Western University · CALondon Health Sciences Centre · CAHokkaido University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although a primary route of breast cancer metastasis is believed to be via lymphatics, the molecular factors involved are poorly understood. We hypothesized that one such factor may be the integrin-binding protein osteopontin (OPN), and we investigated this clinically and experimentally. In breast cancer patients undergoing sentinel lymph node biopsy, OPN levels were significantly higher in lymph node metastases than in the primary tumor (P < 0.001). To test the functional contribution of OPN to lymphatic metastasis and to determine whether the RGD (Arg-Gly-Asp) integrin-binding sequence of OPN is important for this process, we transfected wild-type OPN or mutant OPN (lacking the RGD sequence) into MDA-MB-468 human breast cancer cells. In vitro, cells overexpressing OPN demonstrated increased anchorage-independent growth in soft agar (P = 0.001) and increased RGD-dependent adhesion (P = 0.045). Following mammary fat pad injection of nude mice, cells overexpressing OPN showed increased lymphovascular invasion, lymph node metastases, and lung micrometastases at earlier time points (P = 0.024). Loss of the RGD region partially abrogated this effect in the lymphatics (P = 0.038). These novel findings indicate that OPN is a key molecular player involved in lymphatic metastasis of breast cancer, potentially by affecting RGD-mediated adhesive interactions and by enhancing the establishment/persistence of tumor cells in the lymphatics.

Indexed as

Lymphatic MetastasisAdultAgedAged, 80 and overAnimalsBlotting, NorthernBlotting, WesternBreast NeoplasmsCell AdhesionCell Line, TumorCell ProliferationFemaleFlow CytometryHumansImmunohistochemistryIntegrinsarginyl-glycyl-aspartic acidIntegrinsOligopeptidesOsteopontinSialoglycoproteinsSPP1 protein, humanSpp1 protein, mouse

Identifiers

PMID16816376
PMCPMC1698777
OpenAlexW2037691924

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.