Evidence map›Paper›PMID 17471232›Full record

ArticleOncogene2007

Human pancreatic tumor cells are sensitized to ionizing radiation by knockdown of caveolin-1.

N Cordes, S Frick, T B Brunner, C Pilarsky, R Grützmann, B Sipos, G Klöppel, W G McKenna, E J Bernhard

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Effect of radiotherapy on the DNA cargo and cellular uptake mechanisms of extracellular vesicles.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2023
    Review
  6. Review
  7. Review
  8. Article
  9. Extracellular matrix and its therapeutic potential for cancer treatment.Signal transduction and targeted therapy · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

9 authors at 6 institutions in 2 countries.

N CordesOncoRay - Center for Radiation Research in Oncology, Medical Faculty Carl Gustav Carus, Dresden, University of Technology, Dresden, Germany. nils.cordes@oncoray.de
S Frick
T B Brunner
C Pilarsky
R Grützmann
B Sipos
G Klöppel
W G McKenna
E J Bernhard
Kiel University · DEChurchill Hospital · GBFriedrich-Alexander-Universität Erlangen-Nürnberg · DEInstitut für Radiobiologie der BundeswehrOncoRay · DEUniversity of Oxford · GB

Funding

TUMOR RADIOSENSITIZATION BY PRENYLTRANSFERASE INHIBITORSR01CA073820 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BERNHARD, ERIC J · 1998 to 2008
$1.6M
Medical Research Council G0700730NCI NIH HHS R01 CA73820
6 · The paper itself

Abstract

Caveolin-1 (Cav-1) is an integral transmembrane protein and a critical component in interactions of integrin receptors with cytoskeleton-associated and signaling molecules. Since integrin-mediated cell adhesion generates signals conferring radiation resistance, we examined the effects of small interfering RNA-mediated knockdown of Cav-1 alone or in combination with beta1-integrin or focal adhesion kinase (FAK) on radiation survival and proliferation of pancreatic carcinoma cell lines. Irradiation induced Cav-1 expression in PATU8902, MiaPaCa2 and Panc1 cell lines. The cell lines showed significant radiosensitization after knockdown of Cav-1, beta1-integrin or FAK and cholesterol depletion by beta-cyclodextrin relative to nonspecific controls. Under knockdown conditions, proliferation of non-irradiated and irradiated cells was significantly attenuated relative to controls. These findings correlated with changes in expression or phosphorylation of Akt, glycogen synthase kinase 3beta, Paxillin, Src, c-Jun N-terminal kinase and mitogen-activated protein kinase. Analysis of DNA microarray data revealed a Cav-1 overexpression in a subset of pancreatic ductal adenocarcinoma samples. The data presented show, for the first time, that disruption of interactions of Cav-1 with beta1-integrin or FAK affects radiation survival and proliferation of pancreatic carcinoma cells and suggest that Cav-1 is critical to these processes. These results indicate that strategies targeting Cav-1 may be useful as an approach to improve conventional therapies, including radiotherapy, for pancreatic cancer.

Indexed as

Blotting, WesternCaveolin 1Cell AdhesionCell CycleCell ProliferationColony-Forming Units AssayFluorescent Antibody TechniqueFocal Adhesion Kinase 1Gene Expression ProfilingHumansIntegrin beta1Mitogen-Activated Protein KinasesPancreatic NeoplasmsPaxillinPhosphatidylinositol 3-KinasesPhosphorylationCaveolin 1Focal Adhesion Kinase 1Integrin beta1Mitogen-Activated Protein KinasesPaxillinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins pp60(c-src)RNA, Small Interfering

Identifiers

PMID17471232
OpenAlexW2053911419

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.