Evidence map›Paper›PMID 27533936›Full record

ReviewJournal of biomedical research2016

Recent advances in targeting the autotaxin-lysophosphatidate-lipid phosphate phosphatase axis in vivo.

Matthew G K Benesch, Xiaoyun Tang, Ganesh Venkatraman, Raie T Bekele, David N Brindley

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of biomedical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.9field-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

40 citing papers in PubMed, 66 citations in OpenAlex.

  1. Observational
  2. Review
  3. Article
  4. Review
  5. Article
  6. World journal of gastrointestinal oncology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Design and Development of Autotaxin Inhibitors.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  11. International journal of molecular sciences · 2021
    Article
  12. Article
  13. Increased Levels of Renal Lysophosphatidic Acid in Rodent Models with Renal Disease.The Journal of pharmacology and experimental therapeutics · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 1 institution in 2 countries.

Matthew G K BeneschSignal Transduction Research Group, Department of Biochemistry, University of Alberta, T6G 2S2, Canada.
Xiaoyun TangSignal Transduction Research Group, Department of Biochemistry, University of Alberta, T6G 2S2, Canada.
Ganesh VenkatramanSignal Transduction Research Group, Department of Biochemistry, University of Alberta, T6G 2S2, Canada.
Raie T BekeleSignal Transduction Research Group, Department of Biochemistry, University of Alberta, T6G 2S2, Canada.
David N BrindleySignal Transduction Research Group, Department of Biochemistry, University of Alberta, T6G 2S2, Canada. david.brindley@ualberta.ca.
Heritage Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular lysophosphatidate (LPA) is a potent bioactive lipid that signals through six G-protein-coupled receptors. This signaling is required for embryogenesis, tissue repair and remodeling processes. LPA is produced from circulating lysophosphatidylcholine by autotaxin (ATX), and is degraded outside cells by a family of three enzymes called the lipid phosphate phosphatases (LPPs). In many pathological conditions, particularly in cancers, LPA concentrations are increased due to high ATX expression and low LPP activity. In cancers, LPA signaling drives tumor growth, angiogenesis, metastasis, resistance to chemotherapy and decreased efficacy of radiotherapy. Hence, targeting the ATX-LPA-LPP axis is an attractive strategy for introducing novel adjuvant therapeutic options. In this review, we will summarize current progress in targeting the ATX-LPA-LPP axis with inhibitors of autotaxin activity, LPA receptor antagonists, LPA monoclonal antibodies, and increasing low LPP expression. Some of these agents are already in clinical trials and have applications beyond cancer, including chronic inflammatory diseases.

Indexed as

cancerchronic inflammationcytokinesmonoclonal antibodieswound repair

Identifiers

PMID27533936
PMCPMC4946318
OpenAlexW2397803156

What Socratic 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 Socratic graph.