Evidence map›Paper›PMID 33093476›Full record

ArticleCell death & disease2020

BET degrader inhibits tumor progression and stem-like cell growth via Wnt/β-catenin signaling repression in glioma cells.

Tao Tian, Tongqi Guo, Wei Zhen, Jianjun Zou, Fuyong Li

Abstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Targeting BRD4-A Promising Therapeutic Option for Glioblastoma?International journal of molecular sciences · 2026
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  15. Integrating network pharmacology and Mendelian randomization to explore potential targets of matrine against ovarian cancer.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
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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

5 authors.

Tao TianDepartment of Oncology, Shandong Zaozhuang Municipal Hospital, Zaozhuang City, Shandong Province, China.
Tongqi GuoDepartment of Neurosurgery, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province), Shenyang, Liaoning Province, China.
Wei ZhenDepartment of Neurosurgery, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province), Shenyang, Liaoning Province, China.
Jianjun ZouDepartment of Neurosurgery, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province), Shenyang, Liaoning Province, China.
Fuyong LiDepartment of Neurosurgery, The People's Hospital of China Medical University (The People's Hospital of Liaoning Province), Shenyang, Liaoning Province, China. Lifuyong126@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on their histological appearance, gliomas are a very common primary tumor type of the brain and are classified into grades, Grade I to Grade IV, of the World Health Organization. Treatment failure is due to the cancer stem cells (CSC) phenotype maintenance and self-renewal. BET degraders such as ZBC260 represents a novel class of BET inhibitors that act by inducing BET proteins degradation. This study explores the mode of action and effects of ZBC260 in vivo and in vitro against glioma. By inhibiting cell proliferation and inducting cell cycle arrest, the fact that glioma cell lines show sensitivity to ZBC260. Notably, ZBC260 targeted glioma without side effects in vivo. In addition, the stem cell-like properties of glioma cells were inhibited upon ZBC260 treatment. When the mechanism was examined, our findings indicated that Wnt/β-catenin pathway repression is required for ZBC260-induced stem cell-like properties and tumor growth suppression. In conclusion, the growth of tumors and stem cell-like properties were inhibited by ZBC260 via Wnt/β-catenin repression, which suggests ZBC260 as a potential therapeutic agent for glioma.

Indexed as

Wnt Signaling PathwayAnimalsApoptosisbeta CateninBromodomain Containing ProteinsCarcinogenesisCell CycleCell Line, TumorCell ProliferationCell SurvivalCell Transformation, NeoplasticGene Expression Regulation, NeoplasticGliomaHumansMiceNeoplastic Stem Cellsbeta Cateninbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsProteinsWnt Proteins

Identifiers

PMID33093476
PMCPMC7582157

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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.