Evidence map›Paper›PMID 19682598›Full record

ReviewProstaglandins & other lipid mediators2009

Evaluating dual activity LPA receptor pan-antagonist/autotaxin inhibitors as anti-cancer agents in vivo using engineered human tumors.

Xiaoyu Xu, Guanghui Yang, Honglu Zhang, Glenn D Prestwich

Abstract readReview
In one paragraph

Review in Prostaglandins & other lipid mediators, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Mesenchymal stem cells engineered for cancer therapy.Advanced drug delivery reviews · 2012
    Review
  10. Article
  11. Hyaluronic acid-based clinical biomaterials derived for cell and molecule delivery in regenerative medicine.Journal of controlled release : official journal of the Controlled Release Society · 2011
    Review
  12. Hyaluronic acid hydrogels for biomedical applications.Advanced materials (Deerfield Beach, Fla.) · 2011
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
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

4 authors at 1 institution in 1 country.

Xiaoyu XuDepartment of Medicinal Chemistry and The Center for Therapeutic Biomaterials, The University of Utah, Suite 205, Salt Lake City, UT 84108-1257, USA.
Guanghui Yang
Honglu Zhang
Glenn D Prestwich
University of Utah · US

Funding

Phosphoinositide and Inositol Polyphosphate ProbesR01NS029632 · NINDS · UNIVERSITY OF UTAH · PI PRESTWICH, GLENN DOWNES · 1992 to 2007
$2.5M
NINDS NIH HHS R01 NS029632
6 · The paper itself

Abstract

Using an in situ cross-linkable hydrogel that mimics the extracellular matrix (ECM), cancer cells were encapsulated and injected in vivo following a "tumor engineering" strategy for orthotopic xenografts. Specifically, we created several three-dimensional (3D) human tumor xenografts and evaluated the tumor response to BrP-LPA, a novel dual function LPA antagonist/ATX inhibitor (LPAa/ATXi). First, we describe the model system and the optimization of semi-synthetic ECM (sECM) compositions and injection parameters for engineered xenografts. Second, we summarize a study to compare angiogenesis inhibition in vivo, comparing BrP-LPA to the kinase inhibitor sunitinib maleate (Sutent). Third, we compare treatment of engineered breast tumors with LPAa/ATXi alone with treatment with Taxol. Fourth, using a re-optimized sECM for non-small cell lung cancer cells, we created reproducibly sized subcutaneous lung tumors and evaluated their response to treatment with LPAa/ATXi. Fifth, we summarize the data on the use of LPAa/ATXi to treat a model for colon cancer metastasis to the liver. Taken together, these improved, more realistic xenografts show considerable utility for evaluating the potential of novel anti-metastatic, anti-proliferative, and anti-angiogenic compounds that modify signal transduction through the LPA signaling pathway.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsBreast NeoplasmsCarcinoma, Non-Small-Cell LungColonic NeoplasmsEnzyme InhibitorsExtracellular MatrixFemaleHumansHydrogelsLiver NeoplasmsLysophospholipase DLysophospholipidsMaleMiceAngiogenesis InhibitorsAntineoplastic AgentsEnzyme InhibitorsHydrogelsLysophospholipase DLysophospholipidsMultienzyme ComplexesOrganophosphonatesPalmitatesPhosphodiesterase IPhosphoric Diester HydrolasesPyrophosphatasesReceptors, Lysophosphatidic Acid

Identifiers

PMID19682598
PMCPMC2756011
OpenAlexW2026491130

What Socratic 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 Socratic graph.