Evidence map›Paper›PMID 18451162›Full record

ArticleCancer research2008

Frzb, a secreted Wnt antagonist, decreases growth and invasiveness of fibrosarcoma cells associated with inhibition of Met signaling.

Yi Guo, Jun Xie, Elyssa Rubin, Ya-Xiong Tang, Fritz Lin, Xiaolin Zi, Bang H Hoang

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. FRZB: a potential prognostic marker for head and neck squamous cell carcinoma.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  9. FRZB affectsExperimental and therapeutic medicine · 2023
    Article
  10. Article
  11. hapln1aNature communications · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Observational
  17. Article
  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

7 authors at 1 institution in 1 country.

Yi GuoDepartment of Orthopedic Surgery, Chao Family Comprehensive Cancer Center, University of California, Irvine, CA 92868, USA.
Jun Xie
Elyssa Rubin
Ya-Xiong Tang
Fritz Lin
Xiaolin Zi
Bang H Hoang
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Chemoprevention of urinary bladder carcinogenesis by flavokawain AR01CA122558 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI ZI, XIAOLIN · 2008 to 2012
$1.7M
Secreted Wnt Inhibitors in the Biology of OsteosarcomaK08CA116003 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI HOANG, BANG H · 2006 to 2010
$636k
Lycopene & Docetaxel in Prostate Cancer: An IGF-I Receptor Targeting ApproachR21CA129793 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI ZI, XIAOLIN · 2007 to 2008
$336k
Kava extract, Flavokawains and Bladder Cancer PreventionR21CA109428 · NCI · UNIVERSITY OF CALIFORNIA IRVINE · PI ZI, XIAOLIN · 2004 to 2005
$205k
NCI NIH HHS CA-109428NCI NIH HHS CA-116003NCI NIH HHS K08 CA116003NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA122558NCI NIH HHS R21 CA109428NCI NIH HHS R21 CA129793
6 · The paper itself

Abstract

Soft tissue sarcomas (STS) have a strong propensity for aggressive growth and metastasis. We showed that the secreted Wnt antagonist Frzb exhibited potent antitumor activity against prostate cancer, an epithelial type of malignancy. In this study, we further showed the antitumor efficacy of Frzb in STS, a mesenchymal group of cancer. Frzb transfection of HT1080 (fibrosarcoma) and SW872 (liposarcoma) cell lines and their conditioned media resulted in a significant reduction in cellular invasion, motility, and colony formation in soft agar compared with vector control-transfected cells. In a xenograft mouse model, Frzb dramatically suppressed tumor growth of HT1080 cells in nude mice. In a tail-vein injection metastatic model, Frzb-transfected HT1080 cells formed fewer and smaller lung nodules than vector control cells. In addition, we identified new mechanisms for Frzb antitumor activities. Frzb reduced c-Met expression and inhibited Met-mediated signaling, associated with up-regulation of epithelial markers (i.e., keratins 8 and 18) and down-regulation of mesenchymal markers (i.e., vimentin, N-cadherin, fibronectin, Slug, and Twist). Similar to Frzb, silencing of c-Met by short hairpin RNA or using a dominant-negative LRP5 receptor also suppressed Met signaling, leading to reduced cellular motility, invasion, and in vivo tumor growth. Given recent studies indicating an important role of c-Met in sarcoma development and progression, our data showed that Frzb expression was significantly inversely correlated with Met expression in both STS cell lines and tissues. These results suggested the usefulness of Frzb in modulating Met signaling as a new treatment strategy for STS.

Indexed as

Cell ProliferationAnimalsCell AdhesionCell MovementDown-RegulationFibrosarcomaFrizzled-Related ProteinsGene Expression Regulation, NeoplasticGlycoproteinsHumansIntracellular Signaling Peptides and ProteinsMatrix Metalloproteinase 2MiceMice, NudeNeoplasm InvasivenessProto-Oncogene ProteinsFrizzled-Related ProteinsGlycoproteinsIntracellular Signaling Peptides and ProteinsMatrix Metalloproteinase 2MET protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins c-metReceptors, Growth FactorRNA, Small InterferingWnt Proteins

Identifiers

PMID18451162
PMCPMC2824245
OpenAlexW2119432637

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.