Evidence map›Paper›PMID 31477833›Full record

ArticleOncogene2019

The role of microRNA-148a and downstream DLGAP1 on the molecular regulation and tumor progression on human glioblastoma.

Yue Li, Weiguo Li, Xiaomin Zeng, Xuemei Tang, Shan Zhang, Feiya Zhong, Xiangni Peng, Yang Zhong, Thomas J Rosol, Xiyun Deng and 3 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Article
  9. Regulation of Pyroptosis by ncRNA: A Novel Research Direction.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Article
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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

13 authors at 7 institutions in 3 countries.

Yue Li *Department of Pathology and Pathophysiology, Hunan Normal University School of Medicine, Changsha, 410013, China.
Weiguo Li *Department of Statistics, College of Mathematics and Computer Science, Hunan Normal University, Changsha, 410081, China.ORCID http://orcid.org/0000-0002-9345-580X
Xiaomin ZengDepartment of Epidemiology and Health Statistics, Public Health School, Central South University, Changsha, 410078, China.
Xuemei TangDepartment of Pathology and Pathophysiology, Hunan Normal University School of Medicine, Changsha, 410013, China.
Shan ZhangDepartment of Pathology and Pathophysiology, Hunan Normal University School of Medicine, Changsha, 410013, China.
Feiya ZhongDepartment of Genetics, College of Life Science, Wuhan University, Wuhan, 430072, China.
Xiangni PengDepartment of Information and Computing Science, School of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, China.
Yang ZhongDepartment of Information and Computing Science, School of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, China.
Thomas J RosolDepartment of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, 45701, USA.
Xiyun DengDepartment of Pathology and Pathophysiology, Hunan Normal University School of Medicine, Changsha, 410013, China.
Zhonghua LiuDepartment of Biochemistry and Molecular Biology, College of Life Science, Hunan Normal University, Changsha, 410081, China. liuzh@hunnu.edu.cn.
Sihua PengKey Laboratory of Exploration and Utilization of Aquatic Genetic Resources (Shanghai Ocean University), Ministry of Education, Shanghai, 201306, China. shpeng@shou.edu.cn.
Xiaoning PengDepartment of Pathology and Pathophysiology, Hunan Normal University School of Medicine, Changsha, 410013, China. pxiaoning@hunnu.edu.cn.
Hunan Normal University · CNJishou University · CNCentral South University · CNMinistry of Agriculture · FJOhio University · USWuhan University · CNXiangtan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common malignant primary brain tumor in adults. Currently, the prognosis of the patients with GBM is very poor and new molecular targets and treatment strategies are urgently needed to combat it. MicroRNA-148a (miR-148a) has been shown to be dysregulated in certain tumor types. However, the role of miR-148a in the pathogenesis of GBM is not fully understood. Here we comprehensively analyzed the roles of miR-148a, downstream DLGAP1, and their molecular pathways in GBM. We showed that miR-148a promote the proliferation and growth of GBM cells both in vitro and in vivo, and also induced the migration, invasion, and EMT (epithelial-mesenchymal transition) program of GBM cells by directly targeting DLGAP1. Furthermore, we identified 31 new miR-148a targets and found that miR-148a function was mainly involved in the cell adhesion signaling pathway and was associated with nervous system diseases. Our findings provide a new mechanism for miR-148a-mediated GBM cell invasion and reveal previously unreported targets of miR-148a as well as novel miR-148a-mediated regulatory networks in GBM. These results increase the understanding of the role of miR-148a in GBM and may lead to novel therapeutic strategies for GBM.

Indexed as

AnimalsBrain NeoplasmsCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGlioblastomaHeterograftsHumansMiceMicroRNAsNeoplasm InvasivenessSAP90-PSD95 Associated ProteinsDLGAP1 protein, humanMicroRNAsMIRN148 microRNA, humanSAP90-PSD95 Associated Proteins

Identifiers

PMID31477833
OpenAlexW2970672244

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.