Evidence map›Paper›PMID 37250146›Full record

ArticleMedComm2023

Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR-1236/HER2 signaling pathway.

Aiqun Liu, Baohong Jiang, Cailu Song, Qizhi Zhong, Yufan Mo, Ruiqin Yang, Ciyu Chen, Cheng Peng, Fu Peng, Hailin Tang

Open access · goldAbstract read
In one paragraph

Article in MedComm, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
8.6field-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

40 citing papers in PubMed, 56 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

10 authors at 5 institutions in 1 country.

Aiqun LiuDepartment of Neurology School of Clinical Medicine  the First Affiliated Hospital of Guangdong Pharmaceutical University Guangzhou China.
Baohong JiangDepartment of Pharmacy, the First Affiliated Hospital, Hengyang Medical School University of South China Hengyang China.
Cailu SongState Key Laboratory of Oncology in South China Sun Yat-sen University Cancer Center Guangzhou China.
Qizhi ZhongDepartment of Neurology School of Clinical Medicine  the First Affiliated Hospital of Guangdong Pharmaceutical University Guangzhou China.
Yufan MoDepartment of Neurology School of Clinical Medicine  the First Affiliated Hospital of Guangdong Pharmaceutical University Guangzhou China.
Ruiqin YangDepartment of Neurology School of Clinical Medicine  the First Affiliated Hospital of Guangdong Pharmaceutical University Guangzhou China.
Ciyu ChenDepartment of Neurology School of Clinical Medicine  the First Affiliated Hospital of Guangdong Pharmaceutical University Guangzhou China.
Cheng PengState Key Laboratory of Southwestern Chinese Medicine Resources Chengdu University of Traditional Chinese Medicine Chengdu China.
Fu PengWest China School of Pharmacy Sichuan University Chengdu China.
Hailin TangState Key Laboratory of Oncology in South China Sun Yat-sen University Cancer Center Guangzhou China.ORCID https://orcid.org/0000-0002-3206-782X
First Affiliated Hospital of Guangdong Pharmaceutical University · CNSun Yat-sen University · CNChengdu University of Traditional Chinese Medicine · CNFirst Affiliated Hospital of University of South China · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the central nervous system diseases, glioma is one of the most common malignancies around the world. Despite the recent improvements in therapies for glioma, the prognosis of some high-risk glioma remains poor. In glioma, isoliquiritigenin (ISL) is reported to have antioxidative and antitumor activities. However, the potential mechanisms between ISL and circle RNAs (circRNAs) in the glioma tumorigenesis process have not yet been reported. Here, we treated glioma cells with ISL, and circRNA expression levels were detected. Circ0030018 was found significantly downregulated by ISL. Therefore, we explored circ0030018 expression profiles and functions in glioma, finding that circ0030018 was evidently overexpressed in glioma cell lines. Colony formation, CCK-8, and transwell assay made clear that circ0030018 silencing dramatically cut down glioma growth and invasion. Moreover, ROS level was detected to find that circ0030018 silence remarkably enhanced cell oxidative stress in glioma. Mechanism studies were conducted to investigate the underlying basis of circ0030018 function in glioma, unveiling that circ0030018 realized its functions partially through the miR-1236/HER2 signaling in glioma. In conclusion, our study investigated the roles and mechanisms of the ISL on the circ0030018/miR-1236/HER2 pathway in glioma tumorigenesis and progression. Circ0030018 could act as the prospective biologic signature or therapeutic target for glioma.

Indexed as

circ0030018gliomaHER2isoliquiritigeninmiR‐1236

Identifiers

PMID37250146
PMCPMC10220153
OpenAlexW4378575606

What OpenQuestion holds

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LicenceCC BY
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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.