Evidence map›Paper›PMID 30307367›Full record

ReviewTissue barriers2018

Blood Vessel Epicardial Substance (BVES) in junctional signaling and cancer.

Bobak Parang, Joshua J Thompson, Christopher S Williams

Open access · bronzeAbstract readReview
In one paragraph

Review in Tissue barriers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. TheBiology · 2025
    Article
  2. LncRNACentral-European journal of immunology · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. The Transition from Gastric Intestinal Metaplasia to Gastric Cancer InvolvesInternational journal of molecular sciences · 2021
    Article
  7. Article
  8. Review
  9. Review
  10. 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

3 authors at 2 institutions in 1 country.

Bobak Paranga Department of Medicine , Cornell University , New York , NY , USA.
Joshua J Thompsonb Department of Medicine, Division of Gastroenterology , Vanderbilt University , Nashville , TN , USA.
Christopher S Williamsb Department of Medicine, Division of Gastroenterology , Vanderbilt University , Nashville , TN , USA.
Vanderbilt University · USCornell University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Selenium in gastrointestinal inflammatory diseasesR01DK099204 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WILLIAMS, CHRISTOPHER S. · 2014 to 2018
$1.8M
BVES modulation of intestinal homeostasis and tumorigenesis via regulation of Wnt signalingF30DK111107 · NIDDK · VANDERBILT UNIVERSITY · PI THOMPSON, JOSHUA JAMES · 2016 to 2019
$129k
The Role of BVES in Intestinal Repair Programs and Inflammatory Bowel DiseaseF30DK096718 · NIDDK · VANDERBILT UNIVERSITY · PI PARANG, BOBAK · 2012 to 2015
$106k
Modulation of Junctional Signaling by BVES in Colorectal CarcinomaI01BX001426 · VA · VETERANS HEALTH ADMINISTRATION · PI WILLIAMS, CHRISTOPHER S. · 2012 to 2024
–
BLRD VA I01 BX001426NCATS NIH HHS UL1 TR000445NIDDK NIH HHS F30 DK096718NIDDK NIH HHS F30 DK111107NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK099204NIGMS NIH HHS T32 GM007347
6 · The paper itself

Abstract

Blood vessel epicardial substance (BVES) is a tight-junction associated protein that was originally discovered from a cDNA screen of the developing heart. Research over the last decade has shown that not only is BVES is expressed in cardiac and skeletal tissue, but BVES is also is expressed throughout the gastrointestinal epithelium. Mice lacking BVES sustain worse intestinal injury and inflammation. Furthermore, BVES is suppressed in gastrointestinal cancers, and mouse modeling has shown that loss of BVES promotes tumor formation. Recent work from multiple laboratories has revealed that BVES can regulate several molecular pathways, including cAMP, WNT, and promoting the degradation of the oncogene, c-Myc. This review will summarize our current understanding of how BVES regulates the intestinal epithelium and discuss how BVES functions at the molecular level to preserve epithelial phenotypes and suppress tumorigenesis.

Indexed as

AnimalsCarcinogenesisCell Adhesion MoleculesHumansMembrane ProteinsMuscle ProteinsNeoplasmsSignal TransductionTight JunctionsCell Adhesion MoleculesMembrane ProteinsMuscle ProteinsPOPDC1 protein, humanBVEScolitis-associated cancerPOPDC1POPEYE

Identifiers

PMID30307367
PMCPMC6389126
OpenAlexW2897100360

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.