Evidence map›Paper›PMID 29752436›Full record

ArticleCell death & disease2018

FOXM1 contributes to taxane resistance by regulating UHRF1-controlled cancer cell stemness.

Bowen Yuan, Youhong Liu, Xiaohui Yu, Linglong Yin, Yuchong Peng, Yingxue Gao, Qianling Zhu, Tuoyu Cao, Yinke Yang, Xuegong Fan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 57 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 2 institutions in 1 country.

Bowen YuanCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Youhong LiuCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Xiaohui YuCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Linglong YinCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Yuchong PengCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Yingxue GaoCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Qianling ZhuCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Tuoyu CaoCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China.
Yinke YangShenzhen BioScien Pharmaceutical Co. Ltd., Shenzhen, Guangdong, China.
Xuegong FanHunan Key Laboratory of Viral Hepatitis, Xiangya Hospital, Central South University, Xiangya, China.
Xiong LiCenter for Molecular Medicine, Xiangya Hospital, Central South University, Xiangya, China. lixiongxiangya@csu.edu.cn.ORCID 0000-0001-6147-1090
Central South University · CNShenzhen Bioeasy Biotechnology (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapy-induced expansion of cancer stem cells (CSCs) has been identified as one of the most critical factors contributing to therapeutic resistance, but the mechanisms of this adaptation are not fully understood. UHRF1 is a key epigenetic regulator responsible for therapeutic resistance, and controls the self-renewal of stem cells. In the present study, taxane-resistant cancer cells were established and stem-like cancer cells were expanded. UHRF1 was overexpressed in the taxane-resistant cancer cells, which maintained CSC characteristics. UHRF1 depletion overcame taxane resistance in vitro and in vivo. Additionally, FOXM1 has been reported to play a role in therapeutic resistance and the self-renewal of CSCs. FOXM1 and UHRF1 are highly correlated in prostate cancer tissues and cells, FOXM1 regulates CSCs by regulating uhrf1 gene transcription in an E2F-independent manner, and FOXM1 protein directly binds to the FKH motifs at the uhrf1 gene promoter. This present study clarified a novel mechanism by which FOXM1 controls CSCs and taxane resistance through a UHRF1-mediated signaling pathway, and validated FOXM1 and UHRF1 as two potential therapeutic targets to overcome taxane resistance.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBridged-Ring CompoundsCCAAT-Enhancer-Binding ProteinsCell Line, TumorDocetaxelDrug Resistance, NeoplasmForkhead Box Protein M1HEK293 CellsHumansMaleMice, Inbred BALB CMice, NudeNeoplastic Stem CellsPhenotypePromoter Regions, GeneticBridged-Ring CompoundsCCAAT-Enhancer-Binding ProteinsDocetaxelForkhead Box Protein M1taxaneTaxoidsUbiquitin-Protein LigasesUHRF1 protein, human

Identifiers

PMID29752436
PMCPMC5948215
OpenAlexW2799715163

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.