Evidence map›Paper›PMID 17299058›Full record

ArticleGut2007

Deficiency of SPARC suppresses intestinal tumorigenesis in APCMin/+ mice.

Owen J Sansom, Fiona C Mansergh, Martin J Evans, Julie A Wilkins, Alan R Clarke

Open access · greenAbstract read
In one paragraph

Article in Gut, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  5. Re-sensitization of 5-FU resistance by SPARC through negative regulation of glucose metabolism in hepatocellular carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  6. Article
  7. SPARC: a matricellular regulator of tumorigenesis.Journal of cell communication and signaling · 2009
    Article
  8. Article
  9. Article
  10. CpG island methylation profile of pancreatic intraepithelial neoplasia.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2008
    Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Owen J SansomBeatson Institute of Cancer Research, Glasgow, Scotland, UK. o.sansom@beaston.gla.ac.uk
Fiona C Mansergh
Martin J Evans
Julie A Wilkins
Alan R Clarke
Cardiff University · GBCancer Research UK Scotland Institute · GBInstitute of Cancer Research · GB

Funding

Medical Research Council G0301154
6 · The paper itself

Abstract

BACKGROUND AND

aimsSPARC (secreted protein acidic, rich in cysteine) is a matricellular protein that has been found to be activated in a number of human cancers. More recently, it has been shown to be upregulated in human gastric and colorectal cancer. We therefore wished to address the functional importance of SPARC upregulation to intestinal tumorigenesis in vivo.

methodsSPARC upregulation was determined in intestinal adenomas of tumour-prone Apc(Min/+) mice at both the RNA and the protein level. To determine the functional importance of SPARC for intestinal tumorigenesis we then intercrossed Sparc knockout mice with Apc(Min/+) mice (n = 20). Intestinal enterocyte migration was examined using bromodeoxyuridine labelling studies.

resultsLevels of murine Sparc and several related proteins were upregulated in adenomas arising in Apc(Min/+) mice. A deficiency of Sparc strongly suppressed adenoma formation in Apc(Min/+) mice (p>or=0.0001). Importantly, a deficiency of Sparc also accelerated enterocyte migration (p = 0.01), as perturbed slow epithelial migration may underpin adenoma formation in the intestine.

conclusionsThese data implicate Sparc in both cell migration and tumour formation, and identify Sparc as a potential therapeutic target for colorectal cancer.

Indexed as

Cell Transformation, NeoplasticAdenocarcinomaAdenomaAnimalsCell MovementColonColorectal NeoplasmsDisease Models, AnimalEnterocytesIntestinal NeoplasmsMiceMice, Inbred C57BLNeoplasm ProteinsOsteonectinPolymerase Chain ReactionRNA, MessengerNeoplasm ProteinsOsteonectinRNA, MessengerRNA, Neoplasm

Identifiers

PMID17299058
PMCPMC2000234
OpenAlexW2118184806

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.