Evidence map›Paper›PMID 33482772›Full record

ArticleBMC cancer2021

4'-O-Methylbroussochalcone B as a novel tubulin polymerization inhibitor suppressed the proliferation and migration of acute myeloid leukaemia cells.

Ziying Liu, Changshui Wang, Yali Wang, Lei Wang, Yueyuan Zhang, Genquan Yan

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 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

6 authors at 2 institutions in 1 country.

Ziying LiuDepartment of pediatrics, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, China.
Changshui WangDepartment of Clinical & Translational Medicine, Jining Life Science Center, Jining, China.
Yali WangDepartment of Clinical & Translational Medicine, Jining Life Science Center, Jining, China.
Lei WangDepartment of Clinical & Translational Medicine, Jining Life Science Center, Jining, China.
Yueyuan ZhangDepartment of Clinical & Translational Medicine, Jining Life Science Center, Jining, China.
Genquan YanDepartment of pharmacy, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. GQYanSdF1254368@163.com.
Affiliated Hospital of Jining Medical University · CNShandong First Medical University · CN

Funding

Natural Science Foundation of Shandong Province ZR2016HQ21
6 · The paper itself

Abstract

backgroundRecent years, survival rates of human with high-risk acute myeloid leukaemia (AML) have not raised substantially. This research aimed to investigate the role of 4'-O-Methylbroussochalcone B, for the treatment of human AML.

methodsFirstly, we evaluated the effects of six chalcones on AML cells activity by MTT assay. Immunofluorescence staining, tubulin polymerization assay and N,N'-ethylenebis (iodoacetamide) (EBI) competition assay were performed on ML-2 cells. Transwell and apoptosis assay were also utilized in ML-2 cells and OCI-AML5 cells. The expressions of migration-related proteins, apoptosis-related proteins and Wnt/β-catenin pathway were detected by Western Blot.

resultsThe results found six chalcones exhibited the anti-proliferative activity against different AML cell lines. Based on the results of immunofluorescence staining, tubulin polymerization assay and EBI competition assay, 4'-O-Methylbroussochalcone B was discovered to be a novel colchicine site tubulin polymerization inhibitor. 4'-O-Methylbroussochalcone B could induce apoptosis, inhibit proliferation and migration of ML-2 cells and OCI-AML5 cells. The cells were arrested in the G2-M phase by the treatment of 4'-O-Methylbroussochalcone B. In addition, 4'-O-Methylbroussochalcone B regulated MAPK and Wnt/β-catenin pathways in AML cells.

conclusion4'-O-Methylbroussochalcone B might inhibit proliferation and migration of the AML cells by MAPK and Wnt/β-catenin pathways as a tubulin polymerization inhibitor. It is promising for 4'-O-Methylbroussochalcone B to become a new drug to treat AML.

Indexed as

Cell MovementCell ProliferationAntineoplastic Agents, PhytogenicApoptosisChalconeChalconesFabaceaeHumansLeukemia, Myeloid, AcutePlant ExtractsPolymerizationSeedsTubulinTubulin ModulatorsTumor Cells, CulturedWnt Signaling Pathway4'-O-methylbroussochalcone BAntineoplastic Agents, PhytogenicChalconeChalconesPlant ExtractsTubulinTubulin Modulators4′-O-Methylbroussochalcone BAcute myeloid leukaemiaColchicineMigrationTubulin polymerization inhibitor

Identifiers

PMID33482772
PMCPMC7825173
OpenAlexW3122916849

What Socratic holds

Textmetadata
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 Socratic graph.