Evidence map›Paper›PMID 15456519›Full record

ArticleBMC cancer2004

Cytotoxicity of psammaplin A from a two-sponge association may correlate with the inhibition of DNA replication.

Yahong Jiang, Eun-Young Ahn, Seung Hee Ryu, Dong-Kyoo Kim, Jang-Su Park, Hyun Joo Yoon, Song You, Burm-Jong Lee, Dong Seok Lee, Jee H Jung

Abstract read
In one paragraph

Article in BMC cancer, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Natural Products from Tongan Marine Organisms.Molecules (Basel, Switzerland) · 2021
    Review
  3. IκBα targeting promotes oxidative stress-dependent cell death.Journal of experimental & clinical cancer research : CR · 2021
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. An overview of naturally occurring histone deacetylase inhibitors.Current topics in medicinal chemistry · 2015
    Review
  10. Article
  11. Article
  12. Sterols and Terpenoids from Viburnum odoratissimum.Natural products and bioprospecting · 2014
    Article
  13. Psammaplin A inhibits hepatitis C virus NS3 helicase.Journal of natural medicines · 2013
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

10 authors.

Yahong JiangDepartment of Chemistry and Biohealth Product Research Center, Inje University, Kimhae 621-749, S Korea. yahongjiang@hotmail.com <yahongjiang@hotmail.com>
Eun-Young Ahn
Seung Hee Ryu
Dong-Kyoo Kim
Jang-Su Park
Hyun Joo Yoon
Song You
Burm-Jong Lee
Dong Seok Lee
Jee H Jung

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSV40 DNA replication system is a very useful tool to understand the mechanism of replication, which is a tightly regulated process. Many environmental and cellular factors can induce cell cycle arrest or apoptosis by inhibiting DNA replication. In the course of our search for bioactive metabolites from the marine sponges, psammaplin A was found to have some anticancer properties, the possible mechanism of which was studied.

methodsCell viability was determined by Cell Counting Kit-8 (CCK-8) to count living RAW264.7 cells by combining 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium (WST-8) and 1-methoxy-phenazine methosulfate (1-methoxy-PMS). The effect of psammaplin A on DNA replication was carried out in SV40 DNA replication system in vitro. The activities of topoisomerase I and polymerase alpha-primase were measured by the relaxation of superhelical plasmid DNA and the incorporation of [3H]dTTP to the template respectively. The ssDNA binding activity of RPA was assessed by Gel Mobility Shift Assay (GMSA).

resultsWe have found that psammaplin A delivers significant cytotoxic activity against the RAW264.7 cell line. It was also found that psammaplin A could substantially inhibit SV40 DNA replication in vitro, in which polymerase alpha-primase is one of its main targets.

conclusionTaken together, we suggest that psammaplin A-induced cytotoxicity may correlate with its inhibition on DNA replication. Psammaplin A has the potential to be developed as an anticancer drug.

Indexed as

Topoisomerase II InhibitorsAnimalsCell Line, TumorCell SurvivalDisulfidesDNA Polymerase IDNA PrimaseDNA ReplicationDrug Screening Assays, AntitumorPoriferaSimian virus 40TyrosineVirus ReplicationDisulfidesDNA polymerase alpha-primaseDNA Polymerase IDNA Primasepsammaplin ATopoisomerase II InhibitorsTyrosine

Identifiers

PMID15456519
PMCPMC524492

What OpenQuestion holds

Textmetadata
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.