Evidence map›Paper›PMID 30450809›Full record

ArticleJournal of cellular and molecular medicine2019

Osterix promotes the migration and angiogenesis of breast cancer by upregulation of S100A4 expression.

Shuang Qu, Jiahui Wu, Qianyi Bao, Bing Yao, Rui Duan, Xiang Chen, Lingyun Li, Hongyan Yuan, Yucui Jin, Changyan Ma

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. CaCancers · 2021
    Review
  10. SHP2 regulates the development of intestinal epithelium by modifying OSTERIXFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

10 authors at 3 institutions in 2 countries.

Shuang QuJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Jiahui WuJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.ORCID 0000-0001-8560-9189
Qianyi BaoJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Bing YaoJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Rui DuanJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Xiang ChenDepartment of General Surgery, The Affiliated Yixing Hospital of Jiangsu University, Yixing, China.
Lingyun LiJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Hongyan YuanDepartment of Oncology and Lombardi Comprehensive Cancer Center, Lombardi Comprehensive Cancer Center, Washington, District of Columbia.
Yucui JinJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.
Changyan MaJiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Nanjing, China.ORCID 0000-0002-1609-4609
Nanjing Medical University · CNJiangsu University · CNVince Lombardi Cancer Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a key transcription factor required for bone formation, osterix (OSX) has been reported to be overexpressed in various cancers, however, its roles in breast cancer progression remain poorly understood. In this study, we demonstrated that OSX was highly expressed in metastatic breast cancer cells. Moreover, it could upregulate the expression of S100 calcium binding protein A4 (S100A4) and potentiate breast cancer cell migration and tumor angiogenesis in vitro and in vivo. Importantly, inhibition of S100A4 impaired OSX-induced cell migration and capillary-like tube formation. Restored S100A4 expression rescued OSX-short hairpin RNA-suppressed cell migration and capillary-like tube formation. Moreover, the expression levels of OSX and S100A4 correlated significantly in human breast tumors. Our study suggested that OSX acts as an oncogenic driver in cell migration and tumor angiogenesis, and may serve as a potential therapeutic target for human breast cancer treatment.

Indexed as

Breast NeoplasmsCell LineCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsMCF-7 CellsNeovascularization, PathologicRNA, Small InterferingS100 Calcium-Binding Protein A4Sp7 Transcription FactorTranscriptional ActivationUp-RegulationRNA, Small InterferingS100A4 protein, humanS100 Calcium-Binding Protein A4SP7 protein, humanSp7 Transcription Factorangiogenesisbreast cancermigrationosterixS100A4

Identifiers

PMID30450809
PMCPMC6349213
OpenAlexW2901146111

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.