Evidence map›Paper›PMID 24455684›Full record

ArticleBioMed research international2013

Stat3 upregulates leucine-rich repeat-containing g protein-coupled receptor 4 expression in osteosarcoma cells.

Jia Liu, Wei Wei, Chang-An Guo, Ning Han, Jian-feng Pan, Teng Fei, Zuo-qin Yan

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Clinical value and molecular mechanism of AQGPs in different tumors.Medical oncology (Northwood, London, England) · 2022
    Review
  9. The Role of LGR4 (GPR48) in Normal and Cancer Processes.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Aberrantly expressed LGR4 empowers Wnt signaling in multiple myeloma by hijacking osteoblast-derived R-spondins.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  15. RANK-RANKL signalling in cancer.Bioscience reports · 2016
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 1 country.

Jia LiuDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Wei WeiInstitute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Chang-An GuoDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Ning HanDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Jian-feng PanDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Teng FeiDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zuo-qin YanDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Fudan University · CNSun Yat-sen University · CNShanghai Institutes for Biological Sciences · CNThe First Affiliated Hospital, Sun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activation of signal transducer and activator of transcription 3 (Stat3) signaling is the common hallmark in various human cancers including osteosarcoma. In the present study, according to PCR-based microarrays using cDNA prepared from interleukin-6 (IL-6) treated osteosarcoma cells, we found that leucine-rich repeat-containing G protein-coupled receptor 4 (LGR4) was a transcriptional target of Stat3. Overexpression of Stat3 promoted LGR4 expression, while its deficiency using small interfering RNA (siRNA) reduced LGR4 expression. Furthermore, we identified a Stat3 binding motif located at -556 to -549 bp in the LGR4 promoter that is able to interact with Stat3. Thus, our results suggest a previously unknown Stat3-LGR4 molecular network, which may control osteosarcoma development and progression.

Indexed as

Bone NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticHumansInterleukin-6Microarray AnalysisOsteosarcomaPromoter Regions, GeneticReceptors, G-Protein-CoupledRNA, Small InterferingSTAT3 Transcription FactorInterleukin-6LGR4 protein, humanReceptors, G-Protein-CoupledRNA, Small InterferingSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID24455684
PMCPMC3886594
OpenAlexW2082721503

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.