Evidence map›Paper›PMID 23045288›Full record

ArticleOncogene2013

Human osteosarcoma CD49f(-)CD133(+) cells: impaired in osteogenic fate while gain of tumorigenicity.

M Ying, G Liu, H Shimada, W Ding, W A May, Q He, G B Adams, L Wu

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Pediatric sarcomas.Oncology letters · 2018
    Article
  11. Article
  12. Personalized Identification of Differentially Expressed Modules in Osteosarcoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. CANCER STEM CELLS IN OSTEOSARCOMA.Case orthopaedic journal
    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

8 authors at 3 institutions in 2 countries.

M YingDepartment of Pathology, Children's Hospital Los Angeles Saban Research Institute, Los Angeles, CA, USA.
G Liu
H Shimada
W Ding
W A May
Q He
G B Adams
L Wu
University of Southern California · USChildren's Hospital of Los Angeles · USZhejiang University · CN

Funding

CAK-RARa Signaling in HSC and Leukemic Cell Commitment to DifferentiationR01CA120512 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI WU, LINGTAO · 2008 to 2012
$1.8M
GLI1 and Cancer Stem Cells in Ewing SarcomaR21CA137485 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI MAY, WILLIAM A · 2010 to 2011
$378k
NCI NIH HHS ARRA-R01CA120512NCI NIH HHS R01 CA120512NCI NIH HHS R21 CA137485
6 · The paper itself

Abstract

The biological relationships among self-renewal, tumorigenicity and lineage differentiation of human osteosarcoma-initiating cells (OSIC) remain elusive, making it difficult to identify and distinguish OSIC from osteosarcoma-forming cells (OSFC) for developing OSIC-targeted therapies. Using a new inverse-lineage tracking strategy coupled with serial human-to-mouse xenotransplantation, we identified a subpopulation of osteosarcoma cells with OSIC-like properties and sought to distinguish them from their progeny, OSFC. We found that serial transplantation of cells from different osteosarcoma cell lines and primary osteosarcoma tissues progressively increased the CD49f(+) subpopulation composing the bulk of the osteosarcoma mass. These CD49f(+) cells displayed characteristics of OSFC: limited in vivo tumorigenicity, weak lineage differentiation, more differentiated osteogenic feature and greater chemo-sensitivity. By contrast, their parental CD49f(-)CD133(+) cells had an inhibited osteogenic fate, together with OSIC-like properties of self-renewal, strong tumorigenicity and differentiation to CD49f(+) progeny. Hence, the CD49f(-)CD133(+) phenotype appears to identify OSIC-like cells that possess strong tumorigenicity correlated with an impaired osteogenic fate and the ability to initiate tumor growth through the generation of CD49f(+) progeny. These findings advance our understanding of OSIC-like properties and, for the first time, provide a much-needed distinction between OSIC and OSFC in this cancer.

Indexed as

AC133 AntigenAnimalsAntigens, CDBone NeoplasmsCell Line, TumorCell ProliferationCell Transformation, NeoplasticDrug Resistance, NeoplasmGene ExpressionGlycoproteinsHumansImmunophenotypingIntegrin alpha6MiceNeoplasm MetastasisNeoplastic Stem CellsAC133 AntigenAntigens, CDGlycoproteinsIntegrin alpha6PeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID23045288
PMCPMC3947577
OpenAlexW2006773539

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.