Evidence map›Paper›PMID 30692142›Full record

ReviewJournal of lipid research2019

Lysophosphatidic acid type 2 receptor agonists in targeted drug development offer broad therapeutic potential.

Gabor J Tigyi, Leonard R Johnson, Sue Chin Lee, Derek D Norman, Erzsebet Szabo, Andrea Balogh, Karin Thompson, Alyssa Boler, W Shannon McCool

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of lipid research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Revisiting the role of lysophosphatidic acid in stem cell biology.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  11. Article
  12. Review
  13. LPAR2 receptor activation attenuates radiation-induced disruption of apical junctional complexes and mucosal barrier dysfunction in mouse colon.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  14. Review
  15. Article
  16. 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

9 authors at 2 institutions in 1 country.

Gabor J TigyiDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163 gtigyi@uthsc.edu.
Leonard R JohnsonDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163.
Sue Chin LeeDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163.
Derek D NormanDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163.
Erzsebet SzaboDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163.
Andrea BaloghDepartment of Physiology, University of Tennessee Health Science Center Memphis, Memphis, TN 38163.
Karin ThompsonRxBio Inc. Memphis, TN 38163.
Alyssa BolerRxBio Inc. Memphis, TN 38163.
W Shannon McCoolRxBio Inc. Memphis, TN 38163.
University of Tennessee Health Science Center · USRxBio (United States) · US

Funding

Ligand Recognition by Phospholipid Growth Factor ReceptorsR01CA092160 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2001 to 2022
$5.9M
IND-Enabling Preclinical Development of a New RadiomitigatorU01AI107331 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2013 to 2018
$2.9M
Preclinical Development of a GI Radiation CountermeasureRC2AI087550 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2009 to 2010
$2.3M
Analysis of Radiomitigative Cell SignalingR01AI080405 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2008 to 2012
$2.1M
The anti-diarrheal potential of a LPA analog Rx100R43DK105719 · NIDDK · RXBIO, INC. · PI THOMPSON, KARIN · 2015 to 2015
$223k
BLRD VA I01 BX001187NCI NIH HHS R01 CA092160NIAID NIH HHS R01 AI080405NIAID NIH HHS RC2 AI087550NIAID NIH HHS U01 AI107331NIDDK NIH HHS R43 DK105719
6 · The paper itself

Abstract

The growth factor-like lipid mediator, lysophosphatidic acid (LPA), is a potent signaling molecule that influences numerous physiologic and pathologic processes. Manipulation of LPA signaling is of growing pharmacotherapeutic interest, especially because LPA resembles compounds with drug-like features. The action of LPA is mediated through activation of multiple types of molecular targets, including six G protein-coupled receptors that are clear targets for drug development. However, the LPA signaling has been linked to pathological responses that include promotion of fibrosis, atherogenesis, tumorigenesis, and metastasis. Thus, a question arises: Can we harness, in an LPA-like drug, the many beneficial activities of this lipid without eliciting its dreadful actions? We developed octadecyl thiophosphate (OTP; subsequently licensed as Rx100), an LPA mimic with higher stability in vivo than LPA. This article highlights progress made toward developing analogs like OTP and exploring prosurvival and regenerative LPA signaling. We determined that LPA prevents cell death triggered by various cellular stresses, including genotoxic stressors, and rescues cells condemned to apoptosis. LPA

Indexed as

Amino Acid SequenceAnimalsApoptosisDNA DamageDrug DiscoveryHumansReceptors, Lysophosphatidic AcidSignal TransductionReceptors, Lysophosphatidic Acidapoptosisautotaxindeoxyribonucleic acid damage repairgastric erosionradiation mitigatorRx100secretory diarrhea

Identifiers

PMID30692142
PMCPMC6399510
OpenAlexW2912997222

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.