Evidence map›Paper›PMID 25356871›Full record

ArticleCell death & disease2014

TLX activates MMP-2, promotes self-renewal of tumor spheres in neuroblastoma and correlates with poor patient survival.

P L Chavali, R K R Saini, Q Zhai, D Vizlin-Hodzic, S Venkatabalasubramanian, A Hayashi, E Johansson, Z-j Zeng, S Mohlin, S Påhlman and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Proteases Regulate Cancer Stem Cell Properties and Remodel Their Microenvironment.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Cancer stem cells in neuroblastoma therapy resistance.Cancer drug resistance (Alhambra, Calif.) · 2019
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Nuclear receptors in neural stem/progenitor cell homeostasis.Cellular and molecular life sciences : CMLS · 2017
    Review
  16. Article
  17. Review
  18. Review
  19. Review
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

13 authors at 4 institutions in 4 countries.

P L Chavali1] Sahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden [2] Department of Oncology, University of Cambridge, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
R K R SainiSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
Q ZhaiSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
D Vizlin-HodzicSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
S Venkatabalasubramanian1] Sahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden [2] School of Chemical and Biotechnology, SASTRA University, Thanjavur 613401, India.
A HayashiSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
E JohanssonSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
Z-j Zeng1] Sahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden [2] Molecular Biology Research Center, School of Biological Science and Technology, Central South University, Changsha, China.
S MohlinCenter for Molecular Pathology, Lund University, Skåne University Hospital, Malmö SE 20502, Sweden.
S PåhlmanCenter for Molecular Pathology, Lund University, Skåne University Hospital, Malmö SE 20502, Sweden.
L Hansford1] Program in Cell Biology, Hospital for Sick Children, Toronto, Canada M5G 1X8 [2] Department of Molecular Genetics, University of Toronto, Toronto, Canada M5S 1A8.
D R Kaplan1] Program in Cell Biology, Hospital for Sick Children, Toronto, Canada M5G 1X8 [2] Department of Molecular Genetics, University of Toronto, Toronto, Canada M5S 1A8.
K FunaSahlgrenska Cancer Center at the Sahlgrenska Academy, University of Gothenburg, Box 425, Gothenburg SE 40530, Sweden.
Sahlgrenska University Hospital · SELund University · SEUniversity of Toronto · CACentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear orphan receptor TLX (Drosophila tailless homolog) is essential for the maintenance of neural stem/progenitor cell self-renewal, but its role in neuroblastoma (NB) is not well understood. Here, we show that TLX is essential for the formation of tumor spheres in three different NB cell lines, when grown in neural stem cell media. We demonstrate that the knock down of TLX in IMR-32 cells diminishes its tumor sphere-forming capacity. In tumor spheres, TLX is coexpressed with the neural progenitor markers Nestin, CD133 and Oct-4. In addition, TLX is coexpressed with the migratory neural progenitor markers CD15 and matrix metalloproteinase-2 (MMP-2) in xenografts of primary NB cells from patients. Subsequently, we show the effect of TLX on the proliferative, invasive and migratory properties of IMR-32 cells. We attribute this to the recruitment of TLX to both MMP-2 and Oct-4 gene promoters, which resulted in the respective gene activation. In support of our findings, we found that TLX expression was high in NB patient tissues when compared with normal peripheral nervous system tissues. Further, the Kaplan-Meier estimator indicated a negative correlation between TLX expression and survival in 88 NB patients. Therefore, our results point at TLX being a crucial player in progression of NB, by promoting self-renewal of NB tumor-initiating cells and altering their migratory and invasive properties.

Indexed as

AnimalsBiomarkers, TumorCell HypoxiaCell Line, TumorCell MovementCell ProliferationEnzyme ActivationHumansMatrix Metalloproteinase 2Mice, SCIDNeoplasm InvasivenessNeoplastic Stem CellsNeuroblastomaOctamer Transcription Factor-3Orphan Nuclear ReceptorsPromoter Regions, GeneticBiomarkers, TumorMatrix Metalloproteinase 2NR2E1 protein, humanOctamer Transcription Factor-3Orphan Nuclear ReceptorsPOU5F1 protein, humanReceptors, Cytoplasmic and Nuclear

Identifiers

PMID25356871
PMCPMC4237266
OpenAlexW1975837020

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.