Evidence map›Paper›PMID 27058416›Full record

ArticleOncotarget2016

PEDF inhibits pancreatic tumorigenesis by attenuating the fibro-inflammatory reaction.

Daniel R Principe, Brian DeCant, Andrew M Diaz, Riley J Mangan, Rosa Hwang, Andrew Lowy, Brandon B Shetuni, Bharath K Sreekumar, Chuhan Chung, David J Bentrem and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pigment Epithelium-Derived Factor (PEDF)-Based Therapy Induced Photoreceptor Survival by Stabilizing Choroidal Neovessels in a VEGF Overexpression CNV Rat Model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular Pathogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Kras and Tumor Immunity: Friend or Foe?Cold Spring Harbor perspectives in medicine · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

14 authors at 8 institutions in 1 country.

Daniel R PrincipeUniversity of Illinois College of Medicine, Champaign, IL, USA.
Brian DeCantDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Andrew M DiazDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Riley J ManganDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Rosa HwangDepartment of Surgical Oncology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Andrew LowyDepartment of Surgery, University of California San Diego, San Diego, CA, USA.
Brandon B ShetuniNorthwestern Medicine, Central DuPage Hospital, Winfield, IL, USA.
Bharath K SreekumarDepartment of Medicine, Yale University School of Medicine, New Haven, CT, USA.
Chuhan ChungDepartment of Medicine, Yale University School of Medicine, New Haven, CT, USA.
David J BentremRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Hidayatullah G MunshiRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Barbara JungDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Paul J GrippoDepartment of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Faraz BishehsariDepartment of Medicine, Rush University Medical Center, Chicago, IL, USA.
University of Illinois Chicago · USNorthwestern University · USYale University · USCentral DuPage Hospital · USRush University Medical Center · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, San Diego · USUniversity of Illinois Urbana-Champaign · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
CLINICAL ONCOLOGY RESEARCH TRAINING PROGRAMT32CA079447 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LICHT, JONATHAN D. · 1999 to 2013
$3.1M
Non Invasive Treatment Response Monitoring and molecular characterization of NSCLC using Cell-free DNA isolated by an AC Electrokinetic DeviceR01CA161283 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GRIPPO, PAUL J · 2012 to 2016
$1.8M
Targeting BET Bromodomain in Pancreatic CancerR01CA186885 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MUNSHI, HIDAYATULLAH G. · 2014 to 2017
$1.4M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA161283NCI NIH HHS R01 CA186885NCI NIH HHS T32 CA079447NIDDK NIH HHS P30 DK034989
6 · The paper itself

Abstract

Pancreatic cancer is characterized by a pronounced fibro-inflammatory reaction that has been shown to contribute to cancer progression. Previous reports have demonstrated that pigment epithelium-derived factor (PEDF) has potent tumor suppressive effects in pancreatic cancer, though little is known about the mechanisms by which PEDF limits pancreatic tumorigenesis. We therefore employed human specimens, as well as mouse and in vitro models, to explore the effects of PEDF upon the pancreatic microenvironment. We found that PEDF expression is decreased in human pancreatic cancer samples compared to non-malignant tissue. Furthermore, PEDF-deficient patients displayed increased intratumoral inflammation/fibrosis. In mice, genetic ablation of PEDF increased cerulein-induced inflammation and fibrosis, and similarly enhanced these events in the background of oncogenic KRAS. In vitro, recombinant PEDF neutralized macrophage migration as well as inhibited macrophage-induced proliferation of tumor cells. Additionally, recombinant PEDF suppressed the synthesis of pro-inflammatory/pro-fibrotic cytokines both in vivo and in vitro, and reduced collagen I deposition and TGFβ synthesis by pancreatic stellate cells, consistent with reduced fibrosis. Combined, our results demonstrate that PEDF limits pancreatic cancer progression by attenuating the fibro-inflammatory reaction, and makes restoration of PEDF signaling a potential therapeutic approach to study in pancreatic cancer.

Indexed as

AnimalsCarcinogenesisDisease ProgressionEye ProteinsFibrosisHumansInflammationMiceMice, Inbred C57BLMice, KnockoutNerve Growth FactorsPancreatic NeoplasmsPigment Epithelium-Derived FactorSerpinsTumor MicroenvironmentEye ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorSerpinsfibrosisinflammationKRASpancreatic cancerPEDF

Identifiers

PMID27058416
PMCPMC5053722
OpenAlexW2316214239

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.