Evidence map›Paper›PMID 30481488›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

Autotaxin determines colitis severity in mice and is secreted by B cells in the colon.

Songbai Lin, Abedul Haque, Reben Raeman, Leilei Guo, Peijian He, Timothy L Denning, Bassel El-Rayes, Wouter H Moolenaar, C Chris Yun

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  11. Review
  12. Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.Molecules (Basel, Switzerland) · 2022
    Review
  13. [Value of autotaxin in predicting refractoryZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2022
    Article
  14. LPA suppresses T cell function by altering the cytoskeleton and disrupting immune synapse formation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Survival of Stem Cells and Progenitors in the Intestine Is Regulated by LPACellular and molecular gastroenterology and hepatology · 2022
    Article
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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 6 institutions in 2 countries.

Songbai LinAtlanta Veterans Administration Medical Center, Decatur, Georgia, USA.
Abedul HaqueAtlanta Veterans Administration Medical Center, Decatur, Georgia, USA.
Reben RaemanDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Leilei GuoDivision of Digestive Diseases, Emory University, Atlanta, Georgia, USA.
Peijian HeAtlanta Veterans Administration Medical Center, Decatur, Georgia, USA.
Timothy L DenningInstitute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA.
Bassel El-RayesDepartment of Hematology and Medical Oncology, Emory University, Atlanta, Georgia, USA.
Wouter H MoolenaarDivision of Cell Biology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
C Chris YunAtlanta Veterans Administration Medical Center, Decatur, Georgia, USA.
Emory University · USAtlanta VA Medical Center · USGeorgia State University · USOncode Institute · NLUnited States Department of Veterans Affairs · USUniversity of Pittsburgh · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
The function of lysophosphatidic acid receptor LPA5R in intestinal inflammation and epithelial damageR01DK116799 · NIDDK · EMORY UNIVERSITY · PI YUN, CHANGHYON CHRIS · 2018 to 2022
$2.5M
Role of CD4 T cells in the pathogenesis of non-alcoholic steatohepatitisK01DK110264 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RAEMAN, REBEN · 2017 to 2021
$702k
Regulation of intestinal homeostasis and epithelial barrier by LPAI01BX002540 · VA · VETERANS HEALTH ADMINISTRATION · PI YUN, CHANGHYON CHRIS · 2015 to 2018
–
BLRD VA I01 BX002540NCI NIH HHS P30 CA138292NIDDK NIH HHS K01 DK110264NIDDK NIH HHS R01 DK116799
6 · The paper itself

Abstract

Autotaxin (ATX or ENPP2) is a secreted lysophospholipase D that produces lysophosphatidic acid (LPA), a pleiotropic lipid mediator acting on specific GPCRs. ATX and LPA have been implicated in key (patho)physiologic processes, including embryonic development, lymphocyte homing, inflammation, and cancer progression. Using LPA receptor knockout mice, we previously uncovered a role for LPA signaling in promoting colitis and colorectal cancer. Here, we examined the role of ATX in experimental colitis through inducible deletion of Enpp2 in adult mice. ATX expression was increased upon induction of colitis, whereas ATX deletion reduced the severity of inflammation in both acute and chronic colitis, accompanied by transient weight loss. ATX expression in lymphocytes was strongly reduced in Rag1

Indexed as

AnimalsB-LymphocytesCell Line, TumorCell MovementColitisColonHCT116 CellsHumansInflammationLymphocytesLysophospholipase DLysophospholipidsMaleMiceMice, Inbred C57BLMice, Knockoutlysophosphatidic acidLysophospholipase DLysophospholipidsPhosphoric Diester HydrolasesReceptors, Lysophosphatidic Acidinflammationlymphocyteslysophosphatidic acid

Identifiers

PMID30481488
PMCPMC6404565
OpenAlexW2902304229

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.