Evidence map›Paper›PMID 25065593›Full record

ArticleOncogene2015

Cyr61 silencing reduces vascularization and dissemination of osteosarcoma tumors.

N Habel, M Vilalta, O Bawa, P Opolon, J Blanco, O Fromigué

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Osteosarcoma and Metastasis.Frontiers in oncology · 2021
    Review
  7. The Roles of CCN1/CYR61 in Pulmonary Diseases.International journal of molecular sciences · 2020
    Review
  8. Article
  9. Review
  10. Article
  11. Oncogenic role of SFRP2 in p53-mutant osteosarcoma development via autocrine and paracrine mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

6 authors at 2 institutions in 2 countries.

N Habel1] Inserm U981, Institut de cancérologie Gustave Roussy, Villejuif, France [2] Gustave Roussy, Villejuif, France [3] Université Paris Sud, Orsay, France [4] Université Paris Diderot, Paris, France.
M VilaltaCell therapy group, Institute for Advanced Chemistry of Catalonia (CSIC), Barcelona, Spain.
O Bawa1] Gustave Roussy, Villejuif, France [2] Université Paris Sud, Orsay, France [3] Institut de Recherche Intégrée en cancérologie à Villejuif (IRCIV), Laboratoire de pathologie expérimentale, Gustave Roussy, Villejuif, France.
P Opolon1] Gustave Roussy, Villejuif, France [2] Université Paris Sud, Orsay, France [3] Institut de Recherche Intégrée en cancérologie à Villejuif (IRCIV), Laboratoire de pathologie expérimentale, Gustave Roussy, Villejuif, France.
J Blanco1] Cell therapy group, Institute for Advanced Chemistry of Catalonia (CSIC), Barcelona, Spain [2] Networking Biomedical Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Barcelona, Spain.
O Fromigué1] Inserm U981, Institut de cancérologie Gustave Roussy, Villejuif, France [2] Gustave Roussy, Villejuif, France [3] Université Paris Sud, Orsay, France.
Institut Gustave Roussy · FRInstitute of Advanced Chemistry of Catalonia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is the most prevalent primary pediatric cancer-related bone disease. These tumors frequently develop resistance to chemotherapy and are highly metastatic, leading to poor outcome. Thus, there is a need for new therapeutic strategies that can prevent cell dissemination. We previously showed that CYR61/CCN1 expression in osteosarcoma cells is correlated to aggressiveness both in vitro and in vivo in mouse models, as well as in patients. In this study, we found that CYR61 is a critical contributor to the vascularization of primary tumor. We demonstrate that silencing CYR61, using lentiviral transduction, leads to a significant reduction in expression level of pro-angiogenic markers such as VEGF, FGF2, PECAM and angiopoietins concomitantly to an increased expression of major anti-angiogenic markers such as thrombospondin-1 and SPARC. Matrix metalloproteinase-2 family member expression, a key pathway in osteosarcoma metastatic capacity was also downregulated when CYR61 was downregulated in osteosarcoma cells. Using a metastatic murine model, we show that CYR61 silencing in osteosarcoma cells results in reduced tumor vasculature and slows tumor growth compared with control. We also find that microvessel density correlates with lung metastasis occurrence and that CYR61 silencing in osteosarcoma cells limits the number of metastases. Taken together, our data indicate that CYR61 silencing can blunt the malignant behavior of osteosarcoma tumor cells by limiting primary tumor growth and dissemination process.

Indexed as

AnimalsBone NeoplasmsCell ProliferationCysteine-Rich Protein 61Down-RegulationGene Expression Regulation, NeoplasticHumansMiceMice, Inbred BALB CMice, NudeMice, TransgenicNeoplasm InvasivenessNeoplasm MetastasisNeovascularization, PathologicOsteosarcomaRNA InterferenceCCN1 protein, mouseCysteine-Rich Protein 61

Identifiers

PMID25065593
OpenAlexW2085380764

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.