Evidence map›Paper›PMID 28144039›Full record

ArticleScientific reports2017

Role of KCNB1 in the prognosis of gliomas and autophagy modulation.

Hao-Yuan Wang, Wen Wang, Yan-Wei Liu, Ming-Yang Li, Ting-Yu Liang, Ji-Ye Li, Hui-Min Hu, Yang Lu, Chen Yao, Yong-Yi Ye and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
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  3. Ion Channels in Cancer: Orchestrators of Electrical Signaling and Cellular Crosstalk.Reviews of physiology, biochemistry and pharmacology · 2022
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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

12 authors at 5 institutions in 1 country.

Hao-Yuan WangDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Wen WangChinese Glioma Cooperative Group (CGCG), Beijing, China.
Yan-Wei LiuBeijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Ming-Yang LiBeijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Ting-Yu LiangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Ji-Ye LiBeijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Hui-Min HuBeijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Yang LuDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Chen YaoDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yong-Yi YeDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yong-Zhi WangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China. wyz232@163.com.
Shi-Zhong ZhangDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China. shizhong_zh@163.com.
Capital Medical University · CNSouthern Medical University · CNBeijing Institute of Neurosurgery · CNSecond Affiliated Hospital of Soochow University · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence suggests that ion channel genes play an important role in the progression of gliomas. However, the mechanisms by which ion channel genes influence the progression of glioma are not fully understood. We identified KCNB1 as a novel ion gene, associated with malignant progression and favorable overall survival (OS) and progression-free survival (PFS) in glioma patients from three datasets (CGGA, GSE16011 and REMBRANDT). Moreover, we characterized a novel function of autophagy induction accompanied by increased apoptosis and reduced proliferation and invasion of glioma cells for KCNB1. KEGG pathway analysis and in vitro studies suggested that the ERK pathway is involved in KCNB1-mediated regulation of autophagy, which was confirmed by inhibition of KCNB1-induced autophagy by using a selective ERK1/2 inhibitor (U0126) or siERK1/2. In vivo studies showed that KCNB1 induced autophagy while inhibiting tumor growth and increasing survival. Overall, our studies define KCNB1 as a novel prognostic factor for gliomas that exerts its tumor suppressive function through autophagy induction.

Indexed as

AutophagyApoptosisBrain NeoplasmsButadienesCell Line, TumorDatasets as TopicDisease-Free SurvivalGliomaHumansMAP Kinase Signaling SystemNeoplasm InvasivenessNitrilesPrognosisShab Potassium ChannelsButadienesKCNB1 protein, humanNitrilesShab Potassium ChannelsU 0126

Identifiers

PMID28144039
PMCPMC5428316
OpenAlexW2582377050

What OpenQuestion holds

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LicenceCC BY
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.