Evidence map›Paper›PMID 36908331›Full record

ArticleJournal of immunology and regenerative medicine2018

Compartment resolved proteomics reveals a dynamic matrisome in a biomechanically driven model of pancreatic ductal adenocarcinoma.

Alexander S Barrett, Ori Maller, Michael W Pickup, Valerie M Weaver, Kirk C Hansen

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology and regenerative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Beyond DNA damage: 3D tumor models and the integrin mechanobiology of radioresistance.Journal of experimental & clinical cancer research : CR · 2026
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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 2 institutions in 1 country.

Alexander S BarrettDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, Aurora, Colorado, USA.
Ori MallerDepartment of Surgery, University of California San Francisco, San Francisco, California, USA.
Michael W PickupDepartment of Surgery, University of California San Francisco, San Francisco, California, USA.
Valerie M WeaverDepartment of Surgery, University of California San Francisco, San Francisco, California, USA.
Kirk C HansenDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, Aurora, Colorado, USA.
University of California, San Francisco · USUniversity of Colorado Denver · US

Funding

Molecular and Cellular Mechanisms in CancerT32CA108462 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOGA, ANDREI · 2004 to 2024
$10.4M
Translational Pulmonary Vascular Biology ProgramT32HL007171 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Sonia Castro Flores, Tim Lahm · 1985 to 2026
$9.4M
Advanced Methods to Evaluate Extracellular Matrix and Crosslinking in the Tumor MR33CA183685 · NCI · UNIVERSITY OF COLORADO DENVER · PI HANSEN, KIRK C, WEAVER, VALERIE MARIE · 2014 to 2016
$1.1M
Quadrupole-Orbitrap Mass SpectrometerS10OD021641 · OD · UNIVERSITY OF COLORADO DENVER · PI HANSEN, KIRK C · 2017 to 2017
$600k
Methods for the Analysis of Tumor Extracellular MatrixR21CA132741 · NCI · UNIVERSITY OF COLORADO DENVER · PI HANSEN, KIRK C · 2010 to 2011
$361k
NCI NIH HHS R21 CA132741NCI NIH HHS R33 CA183685NCI NIH HHS T32 CA108462NHLBI NIH HHS T32 HL007171NIH HHS S10 OD021641
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is characterized by a severe fibrotic component that compromises treatment, alters the immune cell profile and contributes to patient mortality. It has been shown that early on in this process, dynamic changes in tissue biomechanics play an integral role in supporting pancreatic cancer development and progression. Despite the acknowledgement of its importance, a granular view of how stromal composition changes during the course of PDAC progression remains largely unknown. To mimic the quasi-mesenchymal phenotype and pronounced desmoplastic response observed clinically, we utilized a genetically engineered mouse model of PDAC that is driven by a Kras

Indexed as

chemical digestionextracellular matrixfibrosismass spectrometrymatrisomePDACproteomicssolid tumor

Identifiers

PMID36908331
PMCPMC10003644
OpenAlexW2801307395

What OpenQuestion holds

Textmetadata
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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.