Evidence map›Paper›PMID 23722544›Full record

ArticleCancer research2013

Extracellular DNA in pancreatic cancer promotes cell invasion and metastasis.

Fushi Wen, Alex Shen, Andrew Choi, Eugene W Gerner, Jiaqi Shi

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
1.9field-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

54 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Inhibitors of Polyphosphate and Neutrophil Extracellular Traps.Seminars in thrombosis and hemostasis · 2024
    Review
  6. Article
  7. Targeting ROS in cancer: rationale and strategies.Nature reviews. Drug discovery · 2024
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. New Perspectives on the Importance of Cell-Free DNA Biology.Diagnostics (Basel, Switzerland) · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Role of Cell-Free DNA and Deoxyribonucleases in Tumor Progression.International journal of molecular sciences · 2021
    Review
  19. Human Recombinant DNase I (PulmozymeInternational journal of molecular sciences · 2021
    Article
  20. Review
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.

Fushi WenDepartment of Surgery, Arizona Cancer Center; BIO5 Institute and Arizona Cancer Center, BIO5 Oro Valley, University of Arizona, Tucson, AZ 85724, USA. fwen@email.arizona.edu
Alex Shen
Andrew Choi
Eugene W Gerner
Jiaqi Shi
University of Arizona · USUniversity of Michigan–Ann Arbor · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
SPORE in Gastrointestinal CancerP50CA095060 · NCI · UNIVERSITY OF ARIZONA · PI GERNER, EUGENE W · 2002 to 2012
$25.3M
Translational Control by eIF3f in Pancreatic CancerR03CA158895 · NCI · UNIVERSITY OF ARIZONA · PI GERNER, EUGENE W · 2011 to 2012
$152k
Role of eIF3f in Pancreatic CancerR03CA133449 · NCI · UNIVERSITY OF ARIZONA · PI SHI, JIAQI · 2008 to 2009
$151k
NCI NIH HHS CA095060NCI NIH HHS CA158895NCI NIH HHS P30 CA023074NCI NIH HHS P50 CA095060NCI NIH HHS R03 CA133449NCI NIH HHS R03 CA158895
6 · The paper itself

Abstract

Aggressive metastasis is the chief cause of the high morbidity and mortality associated with pancreatic cancer, yet the basis for its aggressive behavior remains elusive. Extracellular DNA (exDNA) is a recently discovered component of inflammatory tissue states. Here, we report that exDNA is present on the surface of pancreatic cancer cells where it is critical for driving metastatic behavior. exDNA was abundant on the surface and vicinity of cultured pancreatic cancer cells but absent from normal pancreas cells. Strikingly, treatment of cancer cell cultures with DNase I to degrade DNA nonspecifically reduced metastatic characters associated with matrix attachment, migration, and invasion. We further assessed the role of exDNA in pancreatic cancer metastasis in vivo using an orthotopic xenograft model established by implantation of pancreatic cancer cells expressing firefly luciferase. Noninvasive bioluminescent imaging confirmed that DNase I treatment was sufficient to suppress tumor metastasis. Mechanistic investigations suggested the existence of a positive feedback loop in which exDNA promotes expression of the inflammatory chemokine CXCL8, which leads to higher production of exDNA by pancreatic cancer cells, with a significant reduction in CXCL8 levels achieved by DNase I treatment. Taken together, our results strongly suggest that exDNA contributes to the highly invasive and metastatic character of pancreatic cancer.

Indexed as

AnimalsCell Line, TumorCell MovementDeoxyribonuclease IDNA, NeoplasmHumansInterleukin-8MiceMice, SCIDNeoplasm InvasivenessNeoplasm MetastasisPancreatic NeoplasmsCXCL8 protein, humanDeoxyribonuclease IDNA, NeoplasmInterleukin-8

Identifiers

PMID23722544
PMCPMC3777608
OpenAlexW2170302953

What OpenQuestion holds

Textmetadata
LicenceTDM
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.