Evidence map›Paper›PMID 18680882›Full record

ArticleNeoplasia (New York, N.Y.)2008

Bromodeoxyuridine inhibits cancer cell proliferation in vitro and in vivo.

Lindsay H Levkoff, Gregory P Marshall, Heather H Ross, Maria Caldeira, Brent A Reynolds, Meryem Cakiroglu, Christopher L Mariani, Wolfgang J Streit, Eric D Laywell

Abstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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.

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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. DNA damage signaling, impairment of cell cycle progression, and apoptosis triggered by 5-ethynyl-2'-deoxyuridine incorporated into DNA.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2013
    Article
  13. Characterization of mammary cancer stem cells in the MMTV-PyMT mouse model.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2012
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The War on Cancer rages on.Neoplasia (New York, N.Y.) · 2009
    Article
  19. Article
  20. Neoplasia: the second decade.Neoplasia (New York, N.Y.) · 2008
    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

9 authors.

Lindsay H LevkoffDepartment of Anatomy & Cell Biology, University of Florida, Gainesville, FL 32610, USA.
Gregory P Marshall
Heather H Ross
Maria Caldeira
Brent A Reynolds
Meryem Cakiroglu
Christopher L Mariani
Wolfgang J Streit
Eric D Laywell

Funding

Effect of Thymidine Analogs on Neural Stem/Progenitor CellsR21NS056019 · NINDS · UNIVERSITY OF FLORIDA · PI LAYWELL, ERIC DION · 2006 to 2007
$323k
NINDS NIH HHS NS056019NINDS NIH HHS R21 NS056019
6 · The paper itself

Abstract

The thymidine analog bromodeoxyuridine (BrdU) is incorporated into newly synthesized DNA and has been shown to increase the susceptibility of incorporating cells to ionizing radiation. However, in the absence of secondary stressors, BrdU is thought to substitute relatively benignly for thymidine and is commonly used to "birth-date" proliferative cells. We report a novel antiproliferative effect of BrdU on cancer cells, which is independent of its role in radiosensitization. A single, brief in vitro exposure to BrdU induces a profound and sustained reduction in the proliferation rate of all cancer cells examined. Cells do not die but variably up-regulate some senescence-associated proteins as they accumulate in the G1 phase of the cell cycle. Bromodeoxyuridine also impairs the proliferative capacity of primary tumor-initiating human glioma cells and may therefore represent a means of targeting cancer stem cells. Finally, conservative in vivo BrdU regimens--in the absence of any other treatment--significantly suppress the progression of gliomas in the highly aggressive, syngeneic RG2 model. These results suggest that BrdU may have an important role as an adjunctive therapeutic for a wide variety of cancers based on new insights into its effect as a negative regulator of cell cycle progression.

Indexed as

Administration, OralAnimalsBromodeoxyuridineCell CycleCell ProliferationDisease ProgressionGliomaHumansInjections, IntraperitonealInjections, SubcutaneousMaleNeoplasms, ExperimentalNucleosidesRatsRats, Inbred F344Time FactorsBromodeoxyuridineNucleosides

Identifiers

PMID18680882
PMCPMC2504767

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.