Evidence map›Paper›PMID 26565624›Full record

ArticlePloS one2015

HOXB1 Is a Tumor Suppressor Gene Regulated by miR-3175 in Glioma.

Liang Han, Dehua Liu, Zhaohui Li, Nan Tian, Ziwu Han, Guang Wang, Yao Fu, Zhigang Guo, Zifeng Zhu, Chao Du and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  10. MicroRNA signatures associated with lymph node metastasis in intramucosal gastric cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
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  19. The Epigenomics of Pituitary Adenoma.Frontiers in endocrinology · 2019
    Review
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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

11 authors at 3 institutions in 1 country.

Liang HanDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Dehua LiuDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Zhaohui LiDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Nan TianDepartment of Cell Biology, College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Ziwu HanDepartment of Cell Biology, College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Guang WangDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Yao FuDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Zhigang GuoDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Zifeng ZhuDepartment of Interventional Therapy, the First Hospital of Jilin University, Changchun, Jilin, China.
Chao DuDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Yu TianDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Jilin University · CNUnion Hospital · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The HOXB1 gene plays a critical role as an oncogene in diverse tumors. However, the functional role of HOXB1 and the mechanism regulating HOXB1 expression in glioma are not fully understood. A preliminary bioinformatics analysis showed that HOXB1 is ectopically expressed in glioma, and that HOXB1 is a possible target of miR-3175. In this study, we investigated the function of HOXB1 and the relationship between HOXB1 and miR-3175 in glioma. We show that HOXB1 expression is significantly downregulated in glioma tissues and cell lines, and that its expression may be closely associated with the degree of malignancy. Reduced HOXB1 expression promoted the proliferation and invasion of glioma cells, and inhibited their apoptosis in vitro, and the downregulation of HOXB1 was also associated with worse survival in glioma patients. More importantly, HOXB1 was shown experimentally to be a direct target of miR-3175 in this study. The downregulated expression of miR-3175 inhibited cell proliferation and invasion, and promoted apoptosis in glioma. The oncogenicity induced by low HOXB1 expression was prevented by an miR-3175 inhibitor in glioma cells. Our results suggest that HOXB1 functions as a tumor suppressor, regulated by miR-3175 in glioma. These results clarify the pathogenesis of glioma and offer a potential target for its treatment.

Indexed as

Gene Expression Regulation, NeoplasticGenes, Tumor SuppressorApoptosisBrainBrain NeoplasmsCell Line, TumorCell ProliferationGliomaHomeodomain ProteinsHumansMicroRNAsNeoplasm InvasivenessPrognosisRNA InterferenceRNA, Small InterferingHomeodomain ProteinsHOXB1 homeodomain proteinMicroRNAsMIRN3175 microRNA, humanRNA, Small Interfering

Identifiers

PMID26565624
PMCPMC4643923
OpenAlexW2255145384

What OpenQuestion holds

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Registered trials

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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.