Evidence map›Paper›PMID 18472018›Full record

ArticleNitric oxide : biology and chemistry2008

Effect of artemisinins and other endoperoxides on nitric oxide-related signaling pathway in RAW 264.7 mouse macrophage cells.

V Badireenath Konkimalla, Martina Blunder, Bernhard Korn, Shahid A Soomro, Herwig Jansen, Wonsuk Chang, Gary H Posner, Rudolf Bauer, Thomas Efferth

Open access · greenAbstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2008. 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
5.4field-weighted citation impact, top 4% 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, 99 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Plasticity towards Rigidity: A Macrophage Conundrum in Pulmonary Fibrosis.International journal of molecular sciences · 2022
    Review
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  8. The complete chloroplast genome ofMitochondrial DNA. Part B, Resources · 2021
    Article
  9. Sesquiterpene fractions ofIranian journal of basic medical sciences · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Anti-inflammatory, Antioxidant and Antimicrobial Effects of Artemisinin Extracts from Artemisia annua L.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2015
    Article
  16. Treatment of Iron-Loaded Veterinary Sarcoma by Artemisia annua.Natural products and bioprospecting · 2014
    Article
  17. Article
  18. Article
  19. Article
  20. Systems biology of meridians, acupoints, and chinese herbs in disease.Evidence-based complementary and alternative medicine : eCAM · 2012
    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 at 5 institutions in 4 countries.

V Badireenath KonkimallaGerman Cancer Research Center, Pharmaceutical Biology (C015), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Martina Blunder
Bernhard Korn
Shahid A Soomro
Herwig Jansen
Wonsuk Chang
Gary H Posner
Rudolf Bauer
Thomas Efferth
AZ Turnhout · BEGerman Cancer Research Center · DEJohns Hopkins University · USUniversity of Graz · ATHeidelberg University · DE

Funding

Peroxides for Chemotherapy of Malaria and CancerR37AI034885 · NIAID · JOHNS HOPKINS UNIVERSITY · PI POSNER, GARY H · 2006 to 2015
$4.3M
NIAID NIH HHS R37 AI034885
6 · The paper itself

Abstract

Artemisinin is the active principle of the Chinese herb Artemisia annua L. In addition to its anti-malarial activity, artemisinin and its derivatives have been shown to exert profound anti-cancer activity. The endoperoxide moiety in the chemical structure of artemisinin is thought to be responsible for the bioactivity. Here, we analyzed the cytotoxicity and the ability of artemisinin, five of its derivatives, and two other endoperoxides to inhibit generation of nitric oxide (NO). In the RAW 264.7 mouse macrophage cell line, the well-established model cell line to analyze NO generation, artesunate revealed the highest ability to inhibit NO production among all compounds tested. In cytotoxicity assays (XTT assay), the IC(50) value of RAW 264.7 cells for artesunate was determined to be 3.1+/-0.7 microM. In order to associate the cytotoxic effects with specific alteration in gene expression related to NO metabolism and signaling, whole genome mRNA microarray analyses were conducted. RAW 264.7 cells were treated with artesunate using DMSO as vehicle control followed by microarray analysis. A total of 36 genes related to NO metabolism and signaling were found to be differentially expressed upon exposure to artesunate. Apart from NO-related genes, the expression of genes associated with other functional groups was also analyzed. Out of 24 functional groups, differential expression was most prominent in genes involved in cell-to-cell signaling and interactions. Further refinement of this analysis showed that the pathways for cAMP-mediated signaling and Wnt/beta-catenin signaling were most closely related to changes in mRNA expression. In conclusion, NO generation and signaling play a role in exhibiting cytotoxic activity of artesunate. In addition, other signaling pathways also contribute to the inhibitory effect of artesunate towards RAW 264.7 cells pointing to a multi-factorial mode of action of artesunate.

Indexed as

AnimalsArtemisininsCell CommunicationCell DeathCell LineGene Expression ProfilingMacrophagesMiceNitric OxidePeroxidesSignal TransductionArtemisininsNitric OxidePeroxides

Identifiers

PMID18472018
PMCPMC2582405
OpenAlexW2013299486

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.