Evidence map›Paper›PMID 25400746›Full record

ArticleInternational journal of clinical and experimental pathology2014

CXCL12 chemokine expression suppresses human breast cancer growth and metastasis in vitro and in vivo.

Zhi-Dong Lv, Bin Kong, Xiang-Ping Liu, Qian Dong, Hai-Tao Niu, Yong-Hua Wang, Fu-Nian Li, Hai-Bo Wang

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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 24% 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.

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  12. S100A4 participates in epithelial-mesenchymal transition in breast cancer via targeting MMP2.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
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  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Zhi-Dong LvDepartment of Breast Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Bin KongDepartment of Breast Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Xiang-Ping LiuCentral Laboratory of Molecular Biology, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Qian DongDepartment of Pediatric Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Hai-Tao NiuDepartment of Urology Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Yong-Hua WangDepartment of Urology Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Fu-Nian LiDepartment of Breast Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Hai-Bo WangDepartment of Breast Surgery, The Affiliated Hospital of Qingdao University Qingdao 266003, P. R. China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokine receptors are now known to play an important role in cancer growth and metastasis. However, there is little information regarding chemokine expression in breast cancer. The aim of this study was to evaluate CXCL12 expression in breast cancer and to investigate the question of whether reduced expression of CXCL12 may have any pathological significance in breast cancer development or progression. In this study, we performed western blotting and immunohistochemistry to evaluate the expression of CXCL12 and relevance with clinicopathological factors in the invasive ductal carcinoma. Reduction of CXCL12 was significantly correlated with tumor size, lymph node metastasis, TNM stage and Her-2 expression in breast cancer. Patients with negative CXCL12 expression had significantly lower cumulative postoperative 5 year survival rate than those with positive CXCL12 expression. In addition, we demonstrated that upregulation of CXCL12 expression by infection with an adenovirus containing a CXCL12 vector significantly inhibited cell growth and reduced the migration of breast cancer cells. Furthermore, animal studies revealed that nude mice injected with the Ad-CXCL12 cell lines featured a lighter weight than the control cell lines. These data suggest that CXCL12 plays an important role in cell growth and invasion in human breast cancer and it appears to be a potential prognostic marker for patients with breast cancer.

Indexed as

Cell ProliferationAnimalsBreast NeoplasmsCarcinoma, Ductal, BreastChemokine CXCL12FemaleHumansKaplan-Meier EstimateMCF-7 CellsMice, NudeMiddle AgedNeoplasm InvasivenessSignal TransductionTime FactorsTransfectionTumor BurdenChemokine CXCL12CXCL12 protein, humanBreast carcinomaCXCL12growthmetastasisnude mice

Identifiers

PMID25400746
PMCPMC4230065
OpenAlexW1876029972

What OpenQuestion holds

Textmetadata
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.