Evidence map›Paper›PMID 21916995›Full record

ArticleJournal of gastroenterology and hepatology2012

Identification of the putative intestinal stem cell marker doublecortin and CaM kinase-like-1 in Barrett's esophagus and esophageal adenocarcinoma.

Kenneth J Vega, Randal May, Sripathi M Sureban, Stan A Lightfoot, Dongfeng Qu, Alessandra Reed, Nathaniel Weygant, Rama Ramanujam, Rhonda Souza, Mohammad Madhoun and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of gastroenterology and hepatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03526328 (Doublecortin Like Kinase-1 as a Marker and Indicator of Treatment Response for Intestinal Stem Cells in Barrett's Esophagus and Progression to Esophageal Adenocarcinoma), which is not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.6field-weighted citation impact, top 4% 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.

NCT03526328 completednot on this mapstarted 2013, after this paper: background citation

Doublecortin Like Kinase-1 as a Marker and Indicator of Treatment Response for Intestinal Stem Cells in Barrett's Esophagus and Progression to Esophageal Adenocarcinoma

TypeobservationalSponsorUniversity of OklahomaRan2013 to 2019Enrolled32ConditionsBarrett's Esophagus, Esophageal AdenocarcinomaArmsEMR and RFA effect on stem cell marker expression in BE/EAC
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Kelch-like proteins in the gastrointestinal tumors.Acta pharmacologica Sinica · 2023
    Review
  6. Mechanisms and pathophysiology of Barrett oesophagus.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Pancreatic DCLK1Cancer letters · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Analysis of the clinical significance of DCLK1OncoTargets and therapy · 2018
    Article
  20. Dclk1-expressing tuft cells: critical modulators of the intestinal niche?American journal of physiology. Gastrointestinal and liver physiology · 2017
    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

14 authors at 4 institutions in 1 country.

Kenneth J VegaDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Randal May
Sripathi M Sureban
Stan A Lightfoot
Dongfeng Qu
Alessandra Reed
Nathaniel Weygant
Rama Ramanujam
Rhonda Souza
Mohammad Madhoun
Joshua Whorton
Shrikant Anant
Stephen J Meltzer
Courtney W Houchen
University of Oklahoma Health Sciences Center · USJohns Hopkins Medicine · USThe University of Texas Southwestern Medical Center · USUniversity Medical Center · US

Funding

Intestinal Stem Cell Consortium Coordinating CenterU01DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2009 to 2018
$6.5M
Dietary Prevention of CancerR01CA109269 · NCI · WASHINGTON UNIVERSITY · PI ANANT, SHRIKANT · 2005 to 2013
$2.7M
Limited Competition for the Continuation of the Intestinal Stem Cell Consortium Coordinating CenterU24DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2019 to 2023
$2.3M
Isolation and Characterization of Intestinal Stem Cells Using Novel Markers (RP)U01DK085508 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI HOUCHEN, COURTNEY WAYNE · 2009 to 2014
$2.0M
The temporal epigenomic program of Barrett's neoplastic progressionR01DK087454 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI MELTZER, STEPHEN J · 2009 to 2013
$1.8M
PROSTAGLANDIN E2 RECEPTORS IN GASTROINTESTINAL INJURYK08DK002822 · NIDDK · WASHINGTON UNIVERSITY · PI HOUCHEN, COURTNEY WAYNE · 2000 to 2004
$596k
PROSTAGLANDINS AND GASTROINTESTINAL DNA DAMAGER03DK065887 · NIDDK · WASHINGTON UNIVERSITY · PI HOUCHEN, COURTNEY WAYNE · 2004 to 2006
$453k
Pancreatic Stem Cells and CancerR21CA137482 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI HOUCHEN, COURTNEY WAYNE · 2010 to 2011
$346k
NCI NIH HHS R01 CA109269NCI NIH HHS R21 CA137482NIDDK NIH HHS DK087454NIDDK NIH HHS K08 DK002822NIDDK NIH HHS R03 DK065887NIDDK NIH HHS U01 DK085508NIDDK NIH HHS U01 DK085532NIDDK NIH HHS U24 DK085532
6 · The paper itself

Abstract

BACKGROUND AND

aimIn Barrett's esophagus (BE), the normal esophageal squamous epithelium is replaced with a specialized metaplastic columnar epithelium. BE is a premalignant lesion that can progress to esophageal adenocarcinoma (EAC). Currently, there are no early molecular indicators that would predict progression from BE to EAC. As the only permanent residents of the epithelium, stem cells have been implicated in this metaplastic progression. The aim of the present study was to determine the expression of doublecortin and CaM kinase-like-1 (DCAMKL-1) and other putative gastrointestinal stem cell markers in normal esophageal mucosa (NEM), BE, and EAC.

methodsHuman NEM, BE, EAC, and multitissue microarrays were analyzed for DCAMKL-1, and immunohistochemically scored based on staining intensity and tissue involvement, with epithelia and stroma scored separately. Total RNA isolated from BE and paired NEM was subjected to real-time reverse-transcription-polymerase chain reaction analysis for DCAMKL-1, leucine-rich repeat-containing G-protein-coupled receptor (LGR5), and Musashi-1 (Msi-1) mRNA expression.

resultsDCAMKL-1 was minimally expressed in squamous NEM, but increased in BE (with and without dysplasia) and EAC tissues. In EAC, we found increased stromal DCAMKL-1 staining compared to adjacent epithelia. Within the submucosa of dysplastic BE tissues, an increase in the endothelial cell expression of DCAMKL-1 was observed. Finally, an upregulation of DCAMKL-1, LGR5, and Msi-1 mRNA was seen in BE compared to squamous NEM.

conclusionsIn the present study, we report the progressive increase of DCAMKL-1 expression in BE from dysplasia to EAC. Furthermore, there was an increase in putative stem cell markers DCAMKL-1, LGR5, and Msi-1 mRNA. Taken together, these data suggest that the regulation of resident stem cells might play an important role in the progression of BE to EAC.

Indexed as

AdenocarcinomaBarrett EsophagusBiomarkers, TumorDoublecortin-Like KinasesEsophageal NeoplasmsEsophagusHumansIntracellular Signaling Peptides and ProteinsMicroarray AnalysisNerve Tissue ProteinsProtein Serine-Threonine KinasesReceptors, G-Protein-CoupledReverse Transcriptase Polymerase Chain ReactionRNA-Binding ProteinsRNA, MessengerStem CellsBiomarkers, TumorDCLK1 protein, humanDoublecortin-Like KinasesIntracellular Signaling Peptides and ProteinsLGR5 protein, humanMSI1 protein, humanNerve Tissue ProteinsProtein Serine-Threonine KinasesReceptors, G-Protein-CoupledRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID21916995
PMCPMC3289765
OpenAlexW1943370337

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Registered trials

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.