Evidence map›Paper›PMID 21911938›Full record

ArticleThe Journal of clinical investigation2011

BVES regulates EMT in human corneal and colon cancer cells and is silenced via promoter methylation in human colorectal carcinoma.

Christopher S Williams, Baolin Zhang, J Joshua Smith, Ashwath Jayagopal, Caitlyn W Barrett, Christopher Pino, Patricia Russ, Sai H Presley, DunFa Peng, Daniel O Rosenblatt and 9 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

46 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. TheBiology · 2025
    Article
  4. Article
  5. Systemic AAV9.BVES delivery ameliorates muscular dystrophy in a mouse model of LGMDR25.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  6. Review
  7. The Role of POPDC Proteins in Cardiac Pacemaking and Conduction.Journal of cardiovascular development and disease · 2021
    Review
  8. The Transition from Gastric Intestinal Metaplasia to Gastric Cancer InvolvesInternational journal of molecular sciences · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Molecular cancer research : MCR · 2019
    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

19 authors at 2 institutions in 1 country.

Christopher S WilliamsDepartment of Medicine/GI, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA. christopher.williams@vanderbilt.edu
Baolin Zhang
J Joshua Smith
Ashwath Jayagopal
Caitlyn W Barrett
Christopher Pino
Patricia Russ
Sai H Presley
DunFa Peng
Daniel O Rosenblatt
Frederick R Haselton
Jin-Long Yang
M Kay Washington
Xi Chen
Steven Eschrich
Timothy J Yeatman
Wael El-Rifai
R Daniel Beauchamp
Min S Chang
Vanderbilt University · USUniversity of South Florida · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Understanding and Controlling p120 Dysfunction in CRCP50CA095103 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2002 to 2017
$33.6M
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
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
THE ROLE OF ENDOCANNABINOIDS AND THEIR RECEPTORS IN COLORECTAL CANCERP01CA077839 · NCI · VANDERBILT UNIVERSITY · PI DUBOIS, RAYMOND N. · 1999 to 2016
$17.8M
Surgical Oncology Training GrantT32CA106183 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI James Richard Goldenring · 2004 to 2026
$6.0M
REGULATION OF GUT EPITHELIAL CELL PROLIFERATIONR01CA069457 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BEAUCHAMP, ROBERT DANIEL · 1995 to 2016
$4.4M
Chip-Based Diagnosis of Problematic Liver TumorsR01CA112215 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI YEATMAN, TIMOTHY J · 2006 to 2010
$2.3M
The novel adhesion molecule Bves and corneal healingR01EY017185 · NEI · VANDERBILT UNIVERSITY · PI CHANG, MIN S · 2006 to 2010
$1.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR) TL1TL1RR024978 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$1.3M
NCI NIH HHS 5P50CA095103NCI NIH HHS CA068485NCI NIH HHS CA069457NCI NIH HHS CA077839NCI NIH HHS CA106183NCI NIH HHS CA112215NCI NIH HHS P01 CA077839NCI NIH HHS P30 CA068485NCI NIH HHS P30 CA076292NCI NIH HHS P50 CA095103NCI NIH HHS R01 CA069457NCI NIH HHS R01 CA112215NCI NIH HHS T32 CA106183NCRR NIH HHS RR024978NCRR NIH HHS TL1 RR024978NEI NIH HHS EY017185NEI NIH HHS P30 EY008126NEI NIH HHS R01 EY017185NIDDK NIH HHS K08 DK080221NIDDK NIH HHS K08 DK080221-01NIDDK NIH HHS P30 DK058404NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM07347
6 · The paper itself

Abstract

The acquisition of a mesenchymal phenotype is a critical step in the metastatic progression of epithelial carcinomas. Adherens junctions (AJs) are required for suppressing this epithelial-mesenchymal transition (EMT) but less is known about the role of tight junctions (TJs) in this process. Here, we investigated the functions of blood vessel epicardial substance (BVES, also known as POPDC1 and POP1), an integral membrane protein that regulates TJ formation. BVES was found to be underexpressed in all stages of human colorectal carcinoma (CRC) and in adenomatous polyps, indicating its suppression occurs early in transformation. Similarly, the majority of CRC cell lines tested exhibited decreased BVES expression and promoter DNA hypermethylation, a modification associated with transcriptional silencing. Treatment with a DNA-demethylating agent restored BVES expression in CRC cell lines, indicating that methylation represses BVES expression. Reexpression of BVES in CRC cell lines promoted an epithelial phenotype, featuring decreased proliferation, migration, invasion, and anchorage-independent growth; impaired growth of an orthotopic xenograft; and blocked metastasis. Conversely, interfering with BVES function by expressing a dominant-negative mutant in human corneal epithelial cells induced mesenchymal features. These biological outcomes were associated with changes in AJ and TJ composition and related signaling. Therefore, BVES prevents EMT, and its epigenetic silencing may be an important step in promoting EMT programs during colon carcinogenesis.

Indexed as

AdenocarcinomaAdherens JunctionsAnimalsCell Adhesion MoleculesCell Line, TumorColonic NeoplasmsColonic PolypsColorectal NeoplasmsDNA MethylationEpithelial-Mesenchymal TransitionEpithelium, CornealGene ExpressionGene SilencingHumansMembrane ProteinsMiceCell Adhesion MoleculesMembrane ProteinsMuscle ProteinsPOPDC1 protein, human

Identifiers

PMID21911938
PMCPMC3195453
OpenAlexW2032729463

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.