Evidence map›Paper›PMID 24141785›Full record

ArticleOncogene2014

MicroRNA-9 inhibits the proliferation of oral squamous cell carcinoma cells by suppressing expression of CXCR4 via the Wnt/β-catenin signaling pathway.

T Yu, K Liu, Y Wu, J Fan, J Chen, C Li, Q Yang, Z Wang

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 6% 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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 118 citations in OpenAlex.

  1. Pooled it
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  14. CXCL12-CXCR4/CXCR7 Axis in Cancer: from Mechanisms to Clinical Applications.International journal of biological sciences · 2023
    Review
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18 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

T YuDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
K LiuDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
Y WuState Key Laboratory of Oral Diseases, West China College of Stomatology, Sichuan University, Chengdu, People's Republic of China.
J FanDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
J ChenDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
C LiDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
Q YangDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
Z WangDepartment of Head and Neck Oncology Surgery, Sichuan Cancer Hospital, Chengdu, People's Republic of China.
Sichuan Cancer Hospital · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of microRNAs (miRNAs) has been involved in the development and progression of malignancy. MicroRNA-9 (miR-9) has been confirmed to be underexpressed in many types of cancers. However, the relationship between miR-9 and the Wnt/β-catenin signaling pathway in oral squamous cell carcinoma (OSCC) remains largely unknown. Here we showed that the miR-9 was underexpressed in patients with OSCC and several OSCC cell lines. Lentivirus-mediated miR-9 overexpression in highly aggressive (Tca8113 and SCC-9) tumor cells significantly inhibited proliferation of the two cell lines in vitro and in vivo. Furthermore, we found that the CXC chemokine receptor 4 (CXCR4) gene was a direct target of miR-9. RNA interference silencing of CXCR4 proved that miR-9 underexpression led to constitutive activation of β-catenin through activation of CXCR4 expression in OSCC cells. Finally, we also analyzed the possible relationship between miR-9 and the genes downstream of the Wnt/β-catenin pathway in OSCC development and progression. These results provide new evidence of miR-9 as a promising tumor gene therapeutic target for OSCC patients.

Indexed as

Gene Expression Regulation, NeoplasticWnt Signaling Pathway3' Untranslated RegionsAnimalsApoptosisBase SequenceBinding SitesCarcinoma, Squamous CellCell Cycle CheckpointsCell Line, TumorCell ProliferationDown-RegulationGene ExpressionHumansMice, NudeMicroRNAs3' Untranslated RegionsCXCR4 protein, humanMicroRNAsMIRN92 microRNA, humanReceptors, CXCR4

Identifiers

PMID24141785
OpenAlexW2009627966

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.