Evidence map›Paper›PMID 18789157›Full record

ArticleJournal of translational medicine2008

Anti-angiogenic effect of high doses of ascorbic acid.

Nina A Mikirova, Thomas E Ichim, Neil H Riordan

Registry-linked trialAbstract read
In one paragraph

Article in Journal of translational medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01125449 (Phase 2 Study of High Dose Ascorbic Acid in Solid Tumor Disease), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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.

NCT01125449 phase2withdrawnnot on this mapstarted 2020, after this paper: background citation

Phase 2 Study of High Dose Ascorbic Acid in Solid Tumor Disease

TypeinterventionalSponsorSitus Cancer Research CenterRan2020 to 2020Enrolled0ConditionsSarcoma, Adenocarcinoma, Carcinoma, Multiple MyelomaArmsAscorbic acid (vitamin C)
3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Natural approaches in metabolic syndrome management.Archives of medical science : AMS · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Modulation of Cytokines in Cancer Patients by Intravenous Ascorbate Therapy.Medical science monitor : international medical journal of experimental and clinical research · 2016
    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

3 authors.

Nina A MikirovaBio-Communications Research Institute, Wichita, Kansas, USA. nmikirova@brightspot.org
Thomas E Ichim
Neil H Riordan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pharmaceutical doses of ascorbic acid (AA, vitamin C, or its salts) have been reported to exert anticancer activity in vitro and in vivo. One proposed mechanism involves direct cytotoxicity mediated by accumulation of ascorbic acid radicals and hydrogen peroxide in the extracellular environment of tumor cells. However, therapeutic effects have been reported at concentrations insufficient to induce direct tumor cell death. We hypothesized that AA may exert anti-angiogenic effects. To test this, we expanded endothelial progenitor cells (EPCs) from peripheral blood and assessed, whether or not high dose AA would inhibit EPC ability to migrate, change energy metabolism, and tube formation ability. We also evaluated the effects of high dose AA on angiogenic activities of HUVECs (human umbilical vein endothelial cells) and HUAECs (human umbilical arterial endothelial cells). According to our data, concentrations of AA higher than 100 mg/dl suppressed capillary-like tube formation on Matrigel for all cells tested and the effect was more pronounced for progenitor cells in comparison with mature cells. Co-culture of differentiated endothelial cells with progenitor cells showed that there was incorporation of EPCs in vessels formed by HUVECs and HUAECs. Cell migration was assessed using an in vitro wound healing model. The results of these experiments showed an inverse correlation between AA concentrations relative to both cell migration and gap filling capacity. Suppression of NO (nitric oxide) generation appeared to be one of the mechanisms by which AA mediated angiostatic effects. This study supports further investigation into non-cytotoxic antitumor activities of AA.

Indexed as

Angiogenesis InhibitorsAntineoplastic AgentsAscorbic AcidCell MovementCells, CulturedCell SeparationCollagenDose-Response Relationship, DrugDrug CombinationsEndothelial CellsHumansLamininNeovascularization, PhysiologicNG-Nitroarginine Methyl EsterNitric OxideProteoglycansAngiogenesis InhibitorsAntineoplastic AgentsAscorbic AcidCollagenDrug CombinationsLamininmatrigelNG-Nitroarginine Methyl EsterNitric OxideProteoglycans

Identifiers

PMID18789157
PMCPMC2562367

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Registered trials

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.