Evidence map›Paper›PMID 28518151›Full record

ArticleCell death & disease2017

Disulfiram/copper selectively eradicates AML leukemia stem cells in vitro and in vivo by simultaneous induction of ROS-JNK and inhibition of NF-κB and Nrf2.

Bing Xu, Shiyun Wang, Rongwei Li, Kai Chen, Lingli He, Manman Deng, Vinodh Kannappan, Jie Zha, Huijuan Dong, Weiguang Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 142 citations in OpenAlex.

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  14. Involvement of copper in cell death and cancer.Apoptosis : an international journal on programmed cell death · 2025
    Review
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13 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Bing XuDepartment of Hematology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Shiyun WangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Rongwei LiDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Kai ChenDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Lingli HeDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Manman DengDepartment of Hematology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Vinodh KannappanResearch Institute in Healthcare Science, Faculty of Science and Engineering, University of Wolverhampton, Wolverhampton, UK.
Jie ZhaDepartment of Hematology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Huijuan DongDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Weiguang WangResearch Institute in Healthcare Science, Faculty of Science and Engineering, University of Wolverhampton, Wolverhampton, UK.
First Affiliated Hospital of Xiamen University · CNSouthern Medical University · CNNanfang Hospital · CNUniversity of Wolverhampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous malignancy. Despite the advances in past decades, the clinical outcomes of AML patients remain poor. Leukemia stem cells (LSCs) is the major cause of the recurrence of AML even after aggressive treatment making, promoting development of LSC-targeted agents is an urgent clinical need. Although the antitumor activity of disulfiram (DS), an approved anti-alcoholism drug, has been demonstrated in multiple types of tumors including hematological malignancies such as AML, it remains unknown whether this agent would also be able to target cancer stem cells like LSCs. Here, we report the in vitro and in vivo activity of DS in combination with copper (Cu) against CD34

Indexed as

AcetylcysteineADP-ribosyl Cyclase 1AdultAgedAnimalsAntigens, CD34ApoptosisCell Line, TumorCopperDisulfiramFemaleHumansIntracellular SpaceJNK Mitogen-Activated Protein KinasesLeukemia, Myeloid, AcuteMaleAcetylcysteineADP-ribosyl Cyclase 1Antigens, CD34CopperDisulfiramJNK Mitogen-Activated Protein KinasesNFE2L2 protein, humanNF-E2-Related Factor 2NF-kappa BReactive Oxygen Species

Identifiers

PMID28518151
PMCPMC5520701
OpenAlexW2615959728

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.