Evidence map›Paper›PMID 22186140›Full record

ArticleCancer research2012

miR-20a encoded by the miR-17-92 cluster increases the metastatic potential of osteosarcoma cells by regulating Fas expression.

Gangxiong Huang, Kazumasa Nishimoto, Zhichao Zhou, Dennis Hughes, Eugenie S Kleinerman

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

99 citing papers in PubMed, 1 synthesis or guideline pooled it, 168 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. The Role of FAS Receptor Methylation in Osteosarcoma Metastasis.International journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. Noncoding RNAs in apoptosis: identification and function.Turkish journal of biology = Turk biyoloji dergisi · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Role of miRNA-19a in Cancer Diagnosis and Poor Prognosis.International journal of molecular sciences · 2021
    Review
  13. The role of microRNAs in cell death pathways.Yeungnam University journal of medicine · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Noncoding RNAs: the shot callers in tumor immune escape.Signal transduction and targeted therapy · 2020
    Review
  20. Article

39 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Gangxiong HuangDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Kazumasa Nishimoto
Zhichao Zhou
Dennis Hughes
Eugenie S Kleinerman
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
LIPOSOME THERAPY--A POTENTIAL ADJUVANT FOR OSTEOSARCOMAR01CA042992 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KLEINERMAN, EUGENIE S · 1986 to 2010
$3.3M
Regulation of Osteosarcoma Metastasis by Notch and Hes 1 Pathway SignalingR01CA141208 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KLEINERMAN, EUGENIE S · 2011 to 2015
$1.7M
NCI NIH HHS CA 16672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA042992NCI NIH HHS R01 CA141208NCI NIH HHS R01 CA 42992
6 · The paper itself

Abstract

The ability of osteosarcoma cells to form lung metastases has been inversely correlated to cell surface Fas expression. Downregulation of Fas allows osteosarcoma cells to circumvent FasL-mediated apoptosis upon entrance into the FasL(+) lung microenvironment. However, the mechanism of Fas regulation remains unclear. Here, we show that miRNA plays a role in the downregulation of Fas expression in osteosarcoma. Expression levels of several members of the miR-17-92 cluster including miR-20a and miR-19a were found to be higher in metastatic low-Fas-expressing LM7 cells than in the parental nonmetastatic high-Fas-expressing SAOS-2 cells. We also found an inverse correlation between Fas and miR-20a expression in all 8 cell lines derived from patient samples. Overexpression of miR-20a consistently resulted in the downregulation of Fas expression in SAOS-2 cells and thus in decreased sensitivity to FasL. Conversely, inhibiting miR-20a in LM7 cells increased Fas expression and their sensitivity to FasL. Mice injected with LM7 stably transfected with anti-miR-20a had fewer metastases than those with control plasmids. Taken together, our findings suggest that miR-20a, encoded by miR-17-92, downregulates Fas expression in osteosarcoma, thus contributing to the metastatic potential of osteosarcoma cells by altering the phenotype and allowing survival in the FasL(+) lung microenvironment.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBone NeoplasmsCell Line, Tumorfas ReceptorFemaleHumansLung NeoplasmsMiceMice, NudeMicroRNAsOsteosarcomaRNA, Long NoncodingTransfectionFAS protein, humanfas ReceptorMicroRNAsMIR17HG, humanMIRN19A microRNA, humanMIRN20a microRNA, humanMirn20 microRNA, mouseRNA, Long Noncoding

Identifiers

PMID22186140
PMCPMC3288434
OpenAlexW2152325648

What OpenQuestion holds

Textmetadata
LicenceTDM
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.