Evidence map›Paper›PMID 36080255›Full record

ReviewMolecules (Basel, Switzerland)2022

Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.

Souvik Banerjee, Suechin Lee, Derek D Norman, Gabor J Tigyi

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Autotaxin inhibitor IOA-289 reduces gastrointestinal cancer progression in preclinical models.Journal of experimental & clinical cancer research : CR · 2023
    Article
  10. Article
  11. 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

4 authors at 2 institutions in 1 country.

Souvik BanerjeeDepartment of Chemistry, Middle Tennessee State University, 1301 E. Main Street, Murfreesboro, TN 37132, USA.ORCID 0000-0002-7811-2577
Suechin LeeDepartment of Physiology, University of Tennessee Health Science Center Memphis, 3 N. Dunlap Street, Memphis, TN 38163, USA.ORCID 0000-0002-7719-1648
Derek D NormanDepartment of Physiology, University of Tennessee Health Science Center Memphis, 3 N. Dunlap Street, Memphis, TN 38163, USA.ORCID 0000-0002-5626-6399
Gabor J TigyiDepartment of Physiology, University of Tennessee Health Science Center Memphis, 3 N. Dunlap Street, Memphis, TN 38163, USA.ORCID 0000-0001-5371-171X
University of Tennessee Health Science Center · USMiddle Tennessee State University · US

Funding

Risk of Childhood Cancers Associated With Agricultural *R01CA092670 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI CAROZZA, SUSAN E. · 2001 to 2005
$974k
NCI NIH HHS CA092160NCI NIH HHS R01 CA092670
6 · The paper itself

Abstract

The ATX-LPA-LPAR1 signaling pathway plays a universal role in stimulating diverse cellular responses, including cell proliferation, migration, survival, and invasion in almost every cell type. The ATX-LPAR1 axis is linked to several metabolic and inflammatory diseases including cancer, fibrosis, and rheumatoid arthritis. Numerous selective ATX or LPAR1 inhibitors have been developed and so far, their clinical efficacy has only been evaluated in idiopathic pulmonary fibrosis. None of the ATX and LPAR1 inhibitors have advanced to clinical trials for cancer and rheumatoid arthritis. Nonetheless, several research groups, including ours, have shown considerable benefit of simultaneous ATX and LPAR1 inhibition through combination therapy. Recent research suggests that dual-targeting therapies are superior to combination therapies that use two selective inhibitors. However, limited reports are available on ATX-LPAR1 dual inhibitors, potentially due to co-expression of multiple different LPARs with close structural similarities at the same target. In this review, we discuss rational design and future directions of dual ATX-LPAR1 inhibitors.

Indexed as

Arthritis, RheumatoidIdiopathic Pulmonary FibrosisNeoplasmsHumansLysophospholipidsPhosphoric Diester HydrolasesReceptors, Lysophosphatidic AcidLysophospholipidsPhosphoric Diester HydrolasesReceptors, Lysophosphatidic Acidautotaxin (ATX)cancercombination therapydual inhibitorsidiopathic pulmonary fibrosis (IPF)lysophosphatidic acid (LPA)lysophosphatidic acid receptor subtype-1 (LPAR1)metastasis

Identifiers

PMID36080255
PMCPMC9458164
OpenAlexW4293761280

What Socratic holds

Textmetadata
LicenceCC BY
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.