Evidence map›Paper›PMID 32749238›Full record

ArticleThe Journal of clinical investigation2020

Pancreatic ductal adenocarcinoma progression is restrained by stromal matrix.

Honglin Jiang, Robert J Torphy, Katja Steiger, Henry Hongo, Alexa J Ritchie, Mark Kriegsmann, David Horst, Sarah E Umetsu, Nancy M Joseph, Kimberly McGregor and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

92 citing papers in PubMed, 131 citations in OpenAlex.

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32 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

23 authors at 13 institutions in 2 countries.

Honglin JiangDivision of Hematology and Oncology, Department of Medicine and Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
Robert J TorphyDepartment of Surgery, University of Colorado, Aurora, Colorado, USA.
Katja SteigerInstitute of Pathology, School of Medicine, Technical University Munich and German Cancer Consortium (DKTK; partner site Munich), Munich, Germany.
Henry HongoDivision of Hematology and Oncology, Department of Medicine and Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
Alexa J RitchieDivision of Hematology and Oncology, Department of Medicine and Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
Mark KriegsmannDepartment of Pathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
David HorstInstitute of Pathology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Sarah E UmetsuDepartment of Pathology, UCSF, San Francisco, California, USA.
Nancy M JosephDepartment of Pathology, UCSF, San Francisco, California, USA.
Kimberly McGregorFoundation Medicine, Cambridge, Massachusetts, USA.
Michael J PishvaianDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Edik M BlaisPerthera, Inc, McLean, Virginia, USA.
Brian LuBristol-Myers Squibb, Summit, New Jersey, USA.
Mingyu LiBristol-Myers Squibb, Summit, New Jersey, USA.
Michael HollingsworthEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Connor StashkoCenter for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.
Keith VolmarRex Healthcare.
Jen Jen YehLineberger Comprehensive Cancer Center.
Valerie M WeaverCenter for Bioengineering and Tissue Regeneration, UCSF, San Francisco, California, USA.
Zhen J WangDepartment of Radiology and Biomedical Imaging, UCSF, San Francisco, California, USA.
Margaret A TemperoDivision of Hematology and Oncology, Department of Medicine and Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
Wilko WeichertInstitute of Pathology, School of Medicine, Technical University Munich and German Cancer Consortium (DKTK; partner site Munich), Munich, Germany.
Eric A CollissonDivision of Hematology and Oncology, Department of Medicine and Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, USA.
UCSF Helen Diller Family Comprehensive Cancer Center · USBristol-Myers Squibb (United States) · USCalifornia Institute for Regenerative Medicine · USGerman Centre for Cardiovascular Research · DEUniversity of California, San Francisco · USCharité - Universitätsmedizin Berlin · DEFoundation Medicine (United States)Heidelberg University · DEJohns Hopkins University · USRex Medical (United States) · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Nebraska Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Tumor Subtypes and Therapy Response in Pancreatic CancerR01CA199064 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TSAI, SUSAN, YEH, JEN JEN · 2016 to 2021
$4.4M
NRSA Training CoreTL1TR002533 · NCATS · UNIVERSITY OF COLORADO DENVER · PI CICUTTO, LISA · 2018 to 2022
$3.0M
The adaptive kinome in pancreatic cancerR01CA193650 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JOHNSON, GARY L., YEH, JEN JEN · 2015 to 2019
$2.9M
Tension-Stat3-miR-mediated metastasisR01CA192914 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SEEWALDT, VICTORIA L., WEAVER, VALERIE MARIE · 2015 to 2019
$2.9M
Tissue Tension, RANK and Breast Cancer RiskR01CA222508 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HWANG, E.SHELLEY, WEAVER, VALERIE MARIE · 2018 to 2022
$2.8M
Genomics and Functional Characterization of NF1-mutated Lung CancerR01CA227807 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2018 to 2022
$2.8M
Tailoring Therapy to Pancreatic Cancer SubtypesR01CA222862 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2018 to 2022
$1.8M
Crucial Microenvironmental Cofactors for Pancreatic Cancer PathogenesisR01CA178015 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2014 to 2018
$1.5M
NCATS NIH HHS TL1 TR002533NCI NIH HHS R01 CA178015NCI NIH HHS R01 CA193650NCI NIH HHS R01 CA199064NCI NIH HHS R01 CA222508NCI NIH HHS R01 CA222862NCI NIH HHS R01 CA227807
6 · The paper itself

Abstract

Desmoplasia describes the deposition of extensive extracellular matrix and defines primary pancreatic ductal adenocarcinoma (PDA). The acellular component of this stroma has been implicated in PDA pathogenesis and is being targeted therapeutically in clinical trials. By analyzing the stromal content of PDA samples from numerous annotated PDA data sets and correlating stromal content with both anatomic site and clinical outcome, we found PDA metastases in the liver, the primary cause of mortality to have less stroma, have higher tumor cellularity than primary tumors. Experimentally manipulating stromal matrix with an anti-lysyl oxidase like-2 (anti-LOXL2) antibody in syngeneic orthotopic PDA mouse models significantly decreased matrix content, led to lower tissue stiffness, lower contrast retention on computed tomography, and accelerated tumor growth, resulting in diminished overall survival. These studies suggest an important protective role of stroma in PDA and urge caution in clinically deploying stromal depletion strategies.

Indexed as

AgedAnimalsCarcinoma, Pancreatic DuctalExtracellular MatrixFemaleHumansMaleMiceMice, TransgenicMiddle AgedPancreatic NeoplasmsStromal CellsTumor MicroenvironmentCancerExtracellular matrixOncology

Identifiers

PMID32749238
PMCPMC7456216
OpenAlexW3047538947

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.