Evidence map›Paper›PMID 25421212›Full record

ArticleMolecular neurobiology2016

SDF-1/CXCR4 Axis Regulates Cell Cycle Progression and Epithelial-Mesenchymal Transition via Up-regulation of Survivin in Glioblastoma.

Anyan Liao, Ranran Shi, Yuliang Jiang, Suqing Tian, Panpan Li, Fuxi Song, Yalan Qu, Jinna Li, Haiqin Yun, Xiangshan Yang

RetractedAbstract readRetracted Publication
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2016. 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 It has been retracted, and should not be counted.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 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Expression of chemokine receptor CXCR4 is closely correlated with clinical outcome in human nasopharyngeal carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Pooled it
  2. Review
  3. Article
  4. Blockage of glioma cell survival by truncated TEAD-binding domain of YAP.Journal of cancer research and clinical oncology · 2021
    Article
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  7. Article
  8. Review
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  15. Glioblastoma multiforme-derived extracellular vesicles drive normal astrocytes towards a tumour-enhancing phenotype.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Article
  16. Article
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  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Anyan LiaoDepartment of Radiation Oncology, Peking University 3rd Hospital, No. 49 Hua Yuan Bei Lu, Beijing, 100191, China. liaoanyan323@126.com.
Ranran ShiDepartment of General Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Yuliang JiangDepartment of Radiation Oncology, Peking University 3rd Hospital, No. 49 Hua Yuan Bei Lu, Beijing, 100191, China.
Suqing TianDepartment of Radiation Oncology, Peking University 3rd Hospital, No. 49 Hua Yuan Bei Lu, Beijing, 100191, China.
Panpan LiShandong University School of Medicine, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Fuxi SongShandong University School of Medicine, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Yalan QuShandong University School of Medicine, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Jinna LiDepartment of Radiation Oncology, Peking University 3rd Hospital, No. 49 Hua Yuan Bei Lu, Beijing, 100191, China.
Haiqin YunDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Xiangshan YangDepartment of Pathology, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Peking University · CNQilu Hospital of Shandong University · CNShandong First Medical University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stromal cell-derived factor 1 (SDF-1)/CXCR4 ligand-receptor axis is widely recommended as an attractive target for cancer therapy. Meanwhile, epithelial-mesenchymal transition (EMT) process is linked to disease pathophysiology. As one of inhibitors of apoptosis proteins, survivin is implicated in the onset and development of cancer. In the present study, we tried to determine the cause-effect associations between SDF-1/CXCR4 axis and survivin expression in glioblastoma U-251 cell line. Survivin activation and inhibition were induced with exogenous SDF-1 and survivin small interfering RNA (survivin siRNA), respectively. Western blot was used to detect relevant proteins in SDF-1/CXCR4 axis. Western blot analysis revealed that survivin expression in U-251 increased in a dose- and time-dependent manner in response to SDF-1 treatment. However, the interference with MEK/ERK and PI3K/AKT pathway prohibited SDF-1-induced survivin up-regulation. Importantly, survivin knockdown abrogated cell cycle progression and the expression of snail and N-cadherin, compared with non-transfectants. In conclusion, the present study shows that SDF-1 up-regulates survivin via MEK/ERK and PI3K/AKT pathway, leading to cell cycle progression and EMT occurrence dependent on survivin. The blockade of survivin will allow for the treatment of glioblastoma.

Indexed as

Cell CycleCell Line, TumorCell SurvivalChemokine CXCL12Epithelial-Mesenchymal TransitionGlioblastomaHumansInhibitor of Apoptosis ProteinsProto-Oncogene Proteins c-aktReceptors, CXCR4RNA, Small InterferingSurvivinTranscriptional ActivationUp-RegulationBIRC5 protein, humanChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanInhibitor of Apoptosis ProteinsProto-Oncogene Proteins c-aktReceptors, CXCR4RNA, Small InterferingSurvivinCell cycle progressionEMTSDF-1/CXCR4Survivin

Identifiers

PMID25421212
OpenAlexW2740273761

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.