Evidence map›Paper›PMID 16123810›Full record

ReviewOncogene2005

The role of TGF-beta and Wnt signaling in gastrointestinal stem cells and cancer.

Lopa Mishra, Kirti Shetty, Yi Tang, August Stuart, Stephen W Byers

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
5.2field-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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 146 citations in OpenAlex.

  1. Pooled it
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  20. Tumor Dormancy and Slow-Cycling Cancer Cells.Advances in experimental medicine and biology · 2019
    Review

13 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Lopa MishraDepartment of Surgery, Medicine, The Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. lopamishra@yahoo.com
Kirti Shetty
Yi Tang
August Stuart
Stephen W Byers
Georgetown University Medical Center · USGeorgetown University · USWashington DC VA Medical Center · US

Funding

Gastrointestinal Cell Proliferation and Cell CycleR01CA106614 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MISHRA, LOPA · 2005 to 2009
$1.5M
PRAJA-1: A NOVEL ANTI-APOPTOSIS RING FINGER PROTEINR01DK056111 · NIDDK · TEMPLE UNIVERSITY · PI MISHRA, LOPA · 1999 to 2003
$1.2M
Cross Regulation of Beta-catenin and Retinoid SignalingR01DK058196 · NIDDK · GEORGETOWN UNIVERSITY · PI BYERS, STEPHEN W · 2002 to 2004
$844k
NCI NIH HHS R01 CA106614NIDDK NIH HHS R01 DK56111NIDDK NIH HHS R01 DK58196NIDDK NIH HHS R01 DK58637
6 · The paper itself

Abstract

The past three decades have seen an unremitting quest to identify and understand gastrointestinal stem cells, their plasticity in differentiating across cell types, as well as their role in normal, regenerative, and cancer cells. A fascinating hallmark of stem cells is their ability to undergo assymetric cell division, which entails replication of the DNA followed by division of the nucleus and partitioning of the cytoplasm to yield two different daughter cells: a stem cell as well as a committed progenitor cell, the latter proliferating into differentiated progeny. We are only just beginning to understand how normally quiescent, tissue-specific stem cells interpret a vast array of signals to develop into the gastrointestinal system. These signaling pathways include the transforming growth factor-beta (TGF-beta) superfamily, Wnt, FGFs, Hedgehog, Hox proteins that originate from surrounding mesodermal/stromal tissue as well as endodermal/epithelial tissue. TGF-beta and wnt proteins are key morphogens that ultimately influence cell division and cell fate, so that gut endodermal stem cells enter the cell cycle, and undergo cell division that ultimately leads to differentiated cells such as functional hepatocytes, gastric parietal cells, or gut epithelial cells. Disruptions and errors in this process usually lead to tissue-specific gastrointestinal cancers such as hepatocellular cancers, gastric adenocarcinomas, and colonic adenocarcinomas. An increasingly complex and coherent view of stem/progenitor cell signaling networks, which coordinate cell growth, proliferation, stress management, and survival, is helping to define the fragile areas where malignancies are likely to develop and shows promise for the development of better cancer therapies.

Indexed as

AnimalsBone Morphogenetic ProteinsCell DifferentiationGastrointestinal NeoplasmsGastrointestinal TractHumansIntercellular Signaling Peptides and ProteinsMutationReceptors, Transforming Growth Factor betaSignal TransductionSpectrinStem CellsTransforming Growth Factor betaWnt ProteinsBone Morphogenetic ProteinsIntercellular Signaling Peptides and ProteinsReceptors, Transforming Growth Factor betaSpectrinTransforming Growth Factor betaWnt Proteins

Identifiers

PMID16123810
OpenAlexW2140121036

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.