Evidence map›Paper›PMID 26015407›Full record

ArticleOncotarget2015

Anticancer activity of halofuginone in a preclinical model of osteosarcoma: inhibition of tumor growth and lung metastases.

Audrey Lamora, Mathilde Mullard, Jérôme Amiaud, Régis Brion, Dominique Heymann, Françoise Redini, Franck Verrecchia

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. New uses of halofuginone to treat cancer.Journal of pharmaceutical analysis · 2025
    Review
  4. Review
  5. Review
  6. A new insight of immunosuppressive microenvironment in osteosarcoma lung metastasis.Experimental biology and medicine (Maywood, N.J.) · 2023
    Article
  7. Recent and Ongoing Research into Metastatic Osteosarcoma Treatments.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Establishment of a novel human CIC-DUXScientific reports · 2019
    Article
  17. Review
  18. Article
  19. Review
  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

7 authors at 2 institutions in 1 country.

Audrey LamoraINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Mathilde MullardINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Jérôme AmiaudINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Régis BrionINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Dominique HeymannINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Françoise RediniINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Franck VerrecchiaINSERM, UMR 957, Equipe Labellisée Ligue contre le Cancer 2012, Nantes, France.
Inserm · FRLa Ligue Contre le Cancer · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is the main malignant primary bone tumor in children and adolescents for whom the prognosis remains poor, especially when metastases are present at diagnosis. Because we recently demonstrated that TGF-β/Smad cascade plays a crucial role in osteosarcoma metastatic progression, we investigated the effect of halofuginone, identified as an inhibitor of the TGF-β/Smad3 cascade, on osteosarcoma progression. A preclinical model of osteosarcoma was used to evaluate the impact of halofuginone on tumor growth, tumor microenvironment and metastasis development. In vivo experiments showed that halofuginone reduces primary tumor growth and lung metastases development. In vitro experiments demonstrated that halofuginone decreases cell viability mainly by its ability to induce caspase-3 dependent cell apoptosis. Moreover, halofuginone inhibits the TGF-β/Smad3 cascade and the response of TGF-β key targets involved in the metastases dissemination process such as MMP-2. In addition, halofuginone treatment affects the "vicious cycle" established between tumor and bone cells, and therefore the tumor-associated bone osteolysis. Together, these results demonstrate that halofuginone decreased primary osteosarcoma development and associated lung metastases by targeting both the tumor cells and the tumor microenvironment. Using halofuginone may be a promising therapeutic strategy against tumor progression of osteosarcoma specifically against lung metastases dissemination.

Indexed as

AnimalsAntineoplastic AgentsBone NeoplasmsBone RemodelingCell Line, TumorCell ProliferationDisease ProgressionFemaleHumansLung NeoplasmsMiceMice, NudeNeoplasm MetastasisOsteosarcomaPiperidinesQuinazolinonesAntineoplastic AgentshalofuginonePiperidinesQuinazolinonesbone remodelinghalofuginonemetastasesosteosarcomaTGF-β

Identifiers

PMID26015407
PMCPMC4546476
OpenAlexW2149358367

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.