Evidence map›Paper›PMID 16475022›Full record

ArticleClinical & experimental metastasis2005

Metastatic progression of pancreatic cancer: changes in antioxidant enzymes and cell growth.

Anne Lewis, Juan Du, Jingru Liu, Justine M Ritchie, Larry W Oberley, Joseph J Cullen

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical & experimental metastasis, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Molecules (Basel, Switzerland) · 2022
    Review
  3. Frontiers in oncology · 2022
    Review
  4. Review
  5. Apoptotic Effects of Anthocyanins fromInternational journal of molecular sciences · 2021
    Article
  6. Article
  7. The Yin-Yang Regulation of Reactive Oxygen Species and MicroRNAs in Cancer.International journal of molecular sciences · 2019
    Review
  8. Association of Vitamin BProbiotics and antimicrobial proteins · 2019
    Article
  9. Article
  10. Biological activity of PtScientific reports · 2018
    Article
  11. Treating pancreatic cancer: more antioxidants more problems?Expert review of gastroenterology & hepatology · 2018
    Review
  12. Article
  13. Review
  14. Insights into the Dichotomous Regulation of SOD2 in Cancer.Antioxidants (Basel, Switzerland) · 2017
    Review
  15. Superoxide Dismutases in Pancreatic Cancer.Antioxidants (Basel, Switzerland) · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Loss of SOD3 (EcSOD) Expression Promotes an Aggressive Phenotype in Human Pancreatic Ductal Adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    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

6 authors at 2 institutions in 1 country.

Anne LewisUniversity of Iowa College of Medicine, Iowa City, 52242, USA.
Juan Du
Jingru Liu
Justine M Ritchie
Larry W Oberley
Joseph J Cullen
University of Iowa · USUniversity of Iowa Hospitals and Clinics · US

Funding

THERAPIES BASED ON ANTIOXIDANT ENZYME MODULATIONP01CA066081 · NCI · UNIVERSITY OF IOWA · PI OBERLEY, LARRY · 1996 to 2005
$7.7M
Mechanistic Role of Peroxynitrite in Gallbladder DiseaseK08DK060618 · NIDDK · UNIVERSITY OF IOWA · PI CULLEN, JOSEPH J · 2002 to 2004
$377k
NCI NIH HHS CA 66081NIDDK NIH HHS DK 60618
6 · The paper itself

Abstract

Pancreatic cancer has a dismal prognosis due to the fact that patients present late when metastatic disease is already present. Previous studies have demonstrated that pancreatic cancer cells have decreased levels of MnSOD, which correlates well with increased rates of tumor cell proliferation. Recently, we have found that nude mice injected with MIA PaCa-2 human pancreatic cancer cells in the flank occasionally develop ascites and intra-abdominal metastatic deposits. Mice that developed ascites were sacrificed and the ascites cultured. Necropsy demonstrated metastatic tumors in the retroperitoneum, which were excised, digested, and cultured. Western blots, enzyme activity and enzyme activity gels were performed for manganese superoxide dismutase (MnSOD), copper/zinc (CuZnSOD), catalase, and glutathione peroxidase (GPx) in the ascites cell line, metastatic tumor cell line, MIA PaCa-2 primary pancreatic cancer cell line, and the Capan-1, a metastatic pancreatic cancer cell line. Cell growth, plating efficiency, growth in soft agar and growth in nude mice were determined in the ascites, metastatic tumor, and MIA PaCa-2 cell lines. MnSOD, CuZnSOD, and GPx protein and activity were increased in the ascites, metastatic tumor, and Capan-1 cell lines compared to MIA PaCa-2. The ascites and metastatic tumor cell lines had decreased cell growth, plating efficiency, and growth in soft agar, but the ascites cell line had increased cell growth in 4 and 1% O(2) concentrations in vitro and more rapid growth in vivo. Metastatic disease is associated with changes in the content and activity of antioxidant enzymes with an associated change in growth characteristics depending on the O(2) concentrations.

Indexed as

AnimalsCatalaseCell DivisionCell Line, TumorGlutathione PeroxidaseHumansKineticsMiceMice, NudeNeoplasm MetastasisPancreatic NeoplasmsSuperoxide DismutaseTransplantation, HeterologousCatalaseGlutathione PeroxidaseSuperoxide Dismutase

Identifiers

PMID16475022
OpenAlexW2028873536

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.