Evidence map›Paper›PMID 18084615›Full record

ArticleNeoplasia (New York, N.Y.)2007

Statins stimulate in vitro membrane FasL expression and lymphocyte apoptosis through RhoA/ROCK pathway in murine melanoma cells.

Guillaume Sarrabayrouse, Cindy Synaeve, Kevin Leveque, Gilles Favre, Anne-Françoise Tilkin-Mariamé

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Obesity Affects IVF Outcomes and Mevalonic Acid Rescues the Side Effects of Statins on Follicle Growth.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Statins: a repurposed drug to fight cancer.Journal of experimental & clinical cancer research : CR · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Pleiotropic effects of statins: new therapeutic targets in drug design.Naunyn-Schmiedeberg's archives of pharmacology · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  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 4 institutions in 1 country.

Guillaume SarrabayrouseINSERM, U563, Toulouse, F-31300 France.
Cindy Synaeve
Kevin Leveque
Gilles Favre
Anne-Françoise Tilkin-Mariamé
Centre de Physiopathologie de Toulouse-Purpan · FRInserm · FRInstitut Claudius Regaud · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The capacity of FasL molecules expressed on melanoma cells to induce lymphocyte apoptosis contributes to either antitumor immune response or escape depending on their expression level. Little is known, however, about the mechanisms regulating FasL protein expression. Using the murine B16F10 melanoma model weakly positive for FasL, we demonstrated that in vitro treatment with statins, inhibitors of 3-hydroxy-3-methylgutaryl CoA reductase, enhances membrane FasL expression. C3 exotoxin and the geranylgeranyl transferase I inhibitor GGTI-298, but not the farnesyl transferase inhibitor FTI-277, mimic this effect. The capacity of GGTI-298 and C3 exotoxin to inhibit RhoA activity prompted us to investigate the implication of RhoA in FasL expression. Inhibition of RhoA expression by small interfering RNA (siRNA) increased membrane FasL expression, whereas overexpression of constitutively active RhoA following transfection of RhoAV14 plasmid decreased it. Moreover, the inhibition of a RhoA downstream effector p160ROCK also induced this FasL overexpression. We conclude that the RhoA/ROCK pathway negatively regulates membrane FasL expression in these melanoma cells. Furthermore, we have shown that B16F10 cells, through the RhoA/ROCK pathway, promote in vitro apoptosis of Fas-sensitive A20 lymphoma cells. Our results suggest that RhoA/ROCK inhibition could be an interesting target to control FasL expression and lymphocyte apoptosis induced by melanoma cells.

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineADP Ribose TransferasesAmino Acid Chloromethyl KetonesAnimalsApoptosisAtorvastatinBenzamidesBotulinum ToxinsCell Line, TumorFas Ligand Proteinfas ReceptorGene Expression Regulation, NeoplasticHeptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsLymphocytesLymphoma1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine2-methyl-1-((4-methyl-5-isoquinolinyl)sulfonyl)homopiperazineADP Ribose TransferasesAmino Acid Chloromethyl KetonesAtorvastatinBenzamidesbenzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketoneBotulinum Toxinsexoenzyme C3, Clostridium botulinumFas Ligand ProteinFasl protein, mousefas ReceptorFTI 277GGTI 298Heptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsMembrane ProteinsMethionineMevalonic AcidmevalonolactonePyrrolesRecombinant Fusion ProteinsrhoA GTP-Binding ProteinRhoA protein, mouserho-Associated Kinasesrho GTP-Binding ProteinsRNA, Small InterferingRock1 protein, mouseapoptosisFasLMelanomaRhoAstatins

Identifiers

PMID18084615
PMCPMC2134904
OpenAlexW2006296129

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.