Evidence map›Paper›PMID 10468292›Full record

ArticleBritish journal of cancer1999

Wheatgerm agglutinin-mediated toxicity in pancreatic cancer cells.

R E Schwarz, D C Wojciechowicz, A I Picon, M A Schwarz, P B Paty

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

26 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Lectin fromInternational journal of molecular sciences · 2021
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  7. Review
  8. Cytidine MonophosphateJournal of virology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. A New Galactose-Specific Lectin fromIranian journal of biotechnology · 2018
    Article
  13. Characterization of chickpea (Physiology and molecular biology of plants : an international journal of functional plant biology · 2018
    Article
  14. Cancer cell death induced by nanomagnetolectin.European journal of cell biology · 2017
    Article
  15. Plant Lectins as Medical Tools against Digestive System Cancers.International journal of molecular sciences · 2017
    Review
  16. Article
  17. Article
  18. Review
  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

5 authors at 2 institutions in 1 country.

R E SchwarzDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
D C Wojciechowicz
A I Picon
M A Schwarz
P B Paty
Memorial Sloan Kettering Cancer Center · USSouthern California University for Professional Studies · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lectin binding specificities for carbohydrate allow phenotypic and functional characterization of membrane-associated glycoproteins expressed on cancer cells. This analysis examined wheatgerm agglutinin binding to pancreatic cancer cells in vitro and the resulting toxicity. Membrane preparations of nine human pancreatic carcinoma cell lines were studied for lectin binding using wheatgerm agglutinin (WGA), concanavalin A (ConA) and phytohaemagglutinin-L (PHA-L) in a lectin blot analysis. Cell proliferation in vitro was measured by thymidine incorporation in the absence or presence of lectins at various concentrations. Sialic acid binding lectins or succinyl-WGA (succWGA) served as controls. WGA toxicity was tested after swainsonine or neuraminidase pretreatment. Binding and uptake of fluorescein-labelled lectins was studied under fluorescence microscopy. All pancreatic cell lines displayed high WGA membrane binding, primarily to sialic acid residues. Other lectins were bound with weak to moderate intensity only. Lectin toxicity corresponded to membrane binding intensity, and was profound in case of WGA (ID50 at 2.5-5 microg ml(-1)). WGA exposure induced chromatin condensation, nuclear fragmentation and DNA release consistent with apoptosis. Important steps for WGA toxicity included binding to sialic acid on swainsonine-sensitive carbohydrate and lectin internalization. There was rapid cellular uptake and subsequent nuclear relocalization of WGA. In contradistinction to the other lectins studied, WGA proved highly toxic to human pancreatic carcinoma cells in vitro. WGA binding to sialic acid residues of N-linked carbohydrate, cellular uptake and subsequent affinity to N-acetyl glucosamine appear to be necessary steps. Further analysis of this mechanism of profound toxicity may provide insight relevant to the treatment of pancreatic cancer.

Indexed as

Antineoplastic AgentsCell DivisionCell MembraneCell SurvivalChromatinHumansKineticsN-Acetylneuraminic AcidNeuraminidasePancreatic NeoplasmsPhytohemagglutininsTumor Cells, CulturedWheat Germ AgglutininsAntineoplastic AgentsChromatinleukoagglutinins, plantsN-Acetylneuraminic AcidNeuraminidasePhytohemagglutininssuccinyl-WGAWheat Germ Agglutinins

Identifiers

PMID10468292
PMCPMC2363124
OpenAlexW2052121783

What OpenQuestion holds

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LicenceCC BY
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.