Evidence map›Paper›PMID 11259649›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Suppression of ras-mediated transformation and inhibition of tumor growth and angiogenesis by anthrax lethal factor, a proteolytic inhibitor of multiple MEK pathways.

N S Duesbery, J Resau, C P Webb, S Koochekpour, H M Koo, S H Leppla, G F Vande Woude

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-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

32 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. 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

7 authors at 4 institutions in 1 country.

N S DuesberyVan Andel Research Institute, 333 Bostwick Avenue, NE, Grand Rapids, MI 49503, USA. duesbery@vai.org
J Resau
C P Webb
S Koochekpour
H M Koo
S H Leppla
G F Vande Woude
National Cancer Institute · USNational Institute of Dental and Craniofacial Research · USNational Institutes of Health · USVan Andel Institute · US

Funding

TARGETED CYTOTOXIC PROTEINS DERIVED FROM BACTERIAL TOXINSZ01DE000677 · NIDCR · DENTAL &CRANIOFACIAL RESEARCH · PI LEPPLA, STEPHEN H · 1997 to 2002
–
6 · The paper itself

Abstract

Lethal factor is a protease, one component of Bacillus anthracis exotoxin, which cleaves many of the mitogen-activated protein kinase kinases (MEKs). Given the importance of MEK signaling in tumorigenesis, we assessed the effects of anthrax lethal toxin (LeTx) on tumor cells. LeTx was very effective in inhibiting mitogen-activated protein kinase activation in V12 H-ras-transformed NIH 3T3 cells. In vitro, treatment of transformed cells with LeTx caused them to revert to a nontransformed morphology, and inhibited their abilities to form colonies in soft agar and to invade Matrigel without markedly affecting cell proliferation. In vivo, LeTx inhibited growth of ras-transformed cells implanted in athymic nude mice (in some cases causing tumor regression) at concentrations that caused no apparent animal toxicity. Unexpectedly, LeTx also greatly decreased tumor neovascularization. These results demonstrate that LeTx potently inhibits ras-mediated tumor growth and is a potential antitumor therapeutic.

Indexed as

Antigens, Bacterial3T3 CellsAnimalsBacterial ToxinsCarcinogenicity TestsCell DivisionCell Line, TransformedCell Transformation, NeoplasticDisease Models, AnimalMiceMice, NudeMitogen-Activated Protein Kinase KinasesNeoplasm InvasivenessNeoplasms, ExperimentalNeoplasm TransplantationNeovascularization, Physiologicanthrax toxinAntigens, BacterialBacterial ToxinsMitogen-Activated Protein Kinase KinasesPeptide Hydrolasesras Proteins

Identifiers

PMID11259649
PMCPMC31184
OpenAlexW1976885142

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.