Evidence map›Paper›PMID 20007485›Full record

ArticleDisease models & mechanisms

Lack of host SPARC enhances vascular function and tumor spread in an orthotopic murine model of pancreatic carcinoma.

Shanna A Arnold, Lee B Rivera, Andrew F Miller, Juliet G Carbon, Sean P Dineen, Yang Xie, Diego H Castrillon, E Helene Sage, Pauli Puolakkainen, Amy D Bradshaw and 1 more

Abstract read
In one paragraph

Article in Disease models & mechanisms. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 113 citations in OpenAlex.

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  12. Up-regulation of collagen type V alpha 2 (Open medicine (Warsaw, Poland) · 2023
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10 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

11 authors at 4 institutions in 2 countries.

Shanna A ArnoldHamon Center for Therapeutic Oncology Research, Department of Surgery, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Lee B Rivera
Andrew F Miller
Juliet G Carbon
Sean P Dineen
Yang Xie
Diego H Castrillon
E Helene Sage
Pauli Puolakkainen
Amy D Bradshaw
Rolf A Brekken
Benaroya Research InstituteHelsinki University Hospital · FIMedical University of South Carolina · USThe University of Texas Southwestern Medical Center · US

Funding

MECHANISMS OF DRUG ACTION AND DISPOSITIONT32GM007062 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MANGELSDORF, DAVID J · 1985 to 2020
$7.4M
EXTRACELLULAR PROTEINS AS SIGNALS IN ENDOTHELIAL GROWTHR01GM040711 · NIGMS · UNIVERSITY OF WASHINGTON · PI SAGE, EMILY HELENE · 1988 to 2009
$2.7M
Matricellular proteins as regulators of tumor progressionR01CA118240 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BREKKEN, ROLF A · 2007 to 2010
$1.2M
Mentoring and Research in Mouse Models of Cancer and InfertilityK26RR024196 · NCRR · UT SOUTHWESTERN MEDICAL CENTER · PI CASTRILLON, DIEGO H · 2007 to 2011
$616k
NCI NIH HHS R01 CA118240NCI NIH HHS R01CA118240NCRR NIH HHS K26 RR024196NCRR NIH HHS K26RR024196NIGMS NIH HHS GM007062NIGMS NIH HHS R01 GM040711NIGMS NIH HHS R01GM40711NIGMS NIH HHS T32 GM007062
6 · The paper itself

Abstract

Utilizing subcutaneous tumor models, we previously validated SPARC (secreted protein acidic and rich in cysteine) as a key component of the stromal response, where it regulated tumor size, angiogenesis and extracellular matrix deposition. In the present study, we demonstrate that pancreatic tumors grown orthotopically in Sparc-null (Sparc(-/-)) mice are more metastatic than tumors grown in wild-type (Sparc(+/+)) littermates. Tumors grown in Sparc(-/-) mice display reduced deposition of fibrillar collagens I and III, basement membrane collagen IV and the collagen-associated proteoglycan decorin. In addition, microvessel density and pericyte recruitment are reduced in tumors grown in the absence of host SPARC. However, tumors from Sparc(-/-) mice display increased permeability and perfusion, and a subsequent decrease in hypoxia. Finally, we found that tumors grown in the absence of host SPARC exhibit an increase in alternatively activated macrophages. These results suggest that increased tumor burden in the absence of host SPARC is a consequence of reduced collagen deposition, a disrupted vascular basement membrane, enhanced vascular function and an immune-tolerant, pro-metastatic microenvironment.

Indexed as

AnimalsBasement MembraneCell MovementCollagenDisease Models, AnimalExtracellular MatrixMacrophage ActivationMiceMice, KnockoutNeoplasm InvasivenessNeoplasm MetastasisNeovascularization, PathologicOsteonectinPancreatic NeoplasmsPerfusionPermeabilityCollagenOsteonectin

Identifiers

PMID20007485
PMCPMC2806901
OpenAlexW2146122315

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.