Evidence map›Paper›PMID 33579899›Full record

ArticleOncogenesis2021

miR-18a promotes glioblastoma development by down-regulating ALOXE3-mediated ferroptotic and anti-migration activities.

Xinzhi Yang, Jiangang Liu, Chenci Wang, Kenneth King-Yip Cheng, Hongchao Xu, Qingzhong Li, Tian Hua, Xue Jiang, Lili Sheng, Jie Mao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
8.8field-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

54 citing papers in PubMed, 78 citations in OpenAlex.

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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 4 institutions in 2 countries.

Xinzhi Yang *Department of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Jiangang Liu *Department of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Chenci WangSchool of Graduate Studies, Wannan Medical College, Wuhu, Anhui, China.
Kenneth King-Yip ChengDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Hongchao XuDepartment of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Qingzhong LiDepartment of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Tian HuaDepartment of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Xue JiangJoint Laboratory of Guangdong and Hong Kong on Metabolic Diseases, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Lili ShengResearch Center for Cancer, Wannan Medical College, Wuhu, Anhui, China.
Jie MaoDepartment of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China. myw921@yahoo.com.ORCID http://orcid.org/0000-0001-6082-9732
Zhuohao LiuDepartment of Neurosurgery, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, China. lchouhoo@gmail.com.ORCID http://orcid.org/0000-0003-2487-3140
Third Affiliated Hospital of Southern Medical University · CNWannan Medical College · CNGuangdong Pharmaceutical University · CNHong Kong Polytechnic University · HK

Funding

China Postdoctoral Science Foundation 2019M663000National Science Foundation of China | Young Scientists Fund 81900801Shenzhen Science and Technology Innovation Commission 20190805151748954
6 · The paper itself

Abstract

The development of glioblastoma (GBM) is typically accompanied by marked changes in lipid metabolism. Oxylipins and their catalyzed enzymes lipoxygenases (LOXs) have been shown to participate in the development of cancers via multiple pathways, while the understanding of LOXs in GBM remains enigmatic. Thus, we aimed to explore the expression and functional roles of LOXs in the development of GBM. Here we showed that ALOXE3 was markedly down-regulated in human GBM. Knockdown of ALOXE3 in GBM cells fostered the orthotopic tumor growth and shortened lifespan in mice. ALOXE3 deficiency rendered GBM cells resistant to p53-SLC7A11 dependent ferroptosis, promoting GBM cell survival. Mechanistically, miR-18a directly targeted ALOXE3 and suppressed its expression and functions in GBM cells. Furthermore, ALOXE3 silencing promoted 12-hydroxyeicosatetraenoic acids (12-HETE) secretion from GBM cells, in turn, 12-HETE enhanced migration of GBM cells by activating G

Identifiers

PMID33579899
PMCPMC7881152
OpenAlexW3129079324

What OpenQuestion holds

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Read underepoch 390

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.