Evidence map›Paper›PMID 20522640›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2010

Identification of a novel putative pancreatic stem/progenitor cell marker DCAMKL-1 in normal mouse pancreas.

Randal May, Sripathi M Sureban, Stan A Lightfoot, Aimee B Hoskins, Daniel J Brackett, Russell G Postier, Rama Ramanujam, Chinthalapally V Rao, James H Wyche, Shrikant Anant and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
6.2field-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.

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

51 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  20. Pancreatic DCLK1Cancer letters · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Randal MayDept. of Medicine, Univ. of Oklahoma Health Sciences Center, Oklahoma City, 73104, USA.
Sripathi M Sureban
Stan A Lightfoot
Aimee B Hoskins
Daniel J Brackett
Russell G Postier
Rama Ramanujam
Chinthalapally V Rao
James H Wyche
Shrikant Anant
Courtney W Houchen
Cancer Institute (WIA) · INHoward University · USUniversity of Oklahoma Health Sciences Center · US

Funding

Dietary Prevention of CancerR01CA109269 · NCI · WASHINGTON UNIVERSITY · PI ANANT, SHRIKANT · 2005 to 2013
$2.7M
RNA Binding Protein CUGBP2 in Intestinal EpitheliumR01DK062265 · NIDDK · WASHINGTON UNIVERSITY · PI ANANT, SHRIKANT · 2002 to 2010
$1.9M
RNA Binding Proteins in CancerR01CA135559 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI ANANT, SHRIKANT · 2009 to 2013
$1.5M
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 CA-137482NCI NIH HHS R01 CA109269NCI NIH HHS R01 CA135559NCI NIH HHS R21 CA137482NIDDK NIH HHS DK-002822NIDDK NIH HHS DK-065887NIDDK NIH HHS K08 DK002822NIDDK NIH HHS R01 DK062265NIDDK NIH HHS R03 DK065887
6 · The paper itself

Abstract

Stem cells are critical in maintaining adult homeostasis and have been proposed to be the origin of many solid tumors, including pancreatic cancer. Here we demonstrate the expression patterns of the putative intestinal stem cell marker DCAMKL-1 in the pancreas of uninjured C57BL/6 mice compared with other pancreatic stem/progenitor cell markers. We then determined the viability of isolated pancreatic stem/progenitor cells in isotransplantation assays following DCAMKL-1 antibody-based cell sorting. Sorted cells were grown in suspension culture and injected into the flanks of athymic nude mice. Here we report that DCAMKL-1 is expressed in the main pancreatic duct epithelia and islets, but not within acinar cells. Coexpression was observed with somatostatin, NGN3, and nestin, but not glucagon or insulin. Isolated DCAMKL-1+ cells formed spheroids in suspension culture and induced nodule formation in isotransplantation assays. Analysis of nodules demonstrated markers of early pancreatic development (PDX-1), glandular epithelium (cytokeratin-14 and Ep-CAM), and isletlike structures (somatostatin and secretin). These data taken together suggest that DCAMKL-1 is a novel putative stem/progenitor marker, can be used to isolate normal pancreatic stem/progenitors, and potentially regenerates pancreatic tissues. This may represent a novel tool for regenerative medicine and a target for anti-stem cell-based therapeutics in pancreatic cancer.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsBiomarkersCell DifferentiationCell SeparationDoublecortin-Like KinasesEpithelial CellsIntermediate Filament ProteinsMiceMice, Inbred C57BLMice, NudeNerve Tissue ProteinsNestinPancreasProtein Serine-Threonine KinasesSpheroids, CellularBasic Helix-Loop-Helix ProteinsBiomarkersDclk1 protein, mouseDoublecortin-Like KinasesIntermediate Filament ProteinsNerve Tissue ProteinsNes protein, mouseNestinNeurog3 protein, mouseProtein Serine-Threonine Kinases

Identifiers

PMID20522640
PMCPMC2928534
OpenAlexW2118090796

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.