Evidence map›Paper›PMID 30918330›Full record

ArticleOncogene2019

Low doses of decitabine improve the chemotherapy efficacy against basal-like bladder cancer by targeting cancer stem cells.

Mingqing Wu, Lu Sheng, Maosheng Cheng, Haojie Zhang, Yizhou Jiang, Shuibin Lin, Yu Liang, Fengyu Zhu, Zhenqing Liu, Yingyin Zhang and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

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  17. The mStem cells international · 2020
    Article
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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

15 authors at 6 institutions in 2 countries.

Mingqing Wu *Department of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Lu Sheng *Department of Urology, Huadong Hospital, Fudan University, Shanghai, 200040, China.
Maosheng ChengDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Haojie ZhangDepartment of Urology, Huadong Hospital, Fudan University, Shanghai, 200040, China.
Yizhou JiangInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, 518060, China.
Shuibin LinCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Yu LiangDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Fengyu ZhuDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Zhenqing LiuLaboratory of Molecular Signaling, Division of Oral Biology and Medicine, School of Dentistry and Broad Stem Cell Research Center, UCLA, Los Angeles, CA, 90095, USA.
Yingyin ZhangDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Xiuhong ZhangDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Qian GaoDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China.
Demeng ChenCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China. chendm29@mail.sysu.edu.cn.
Jiong LiLaboratory of Molecular Signaling, Division of Oral Biology and Medicine, School of Dentistry and Broad Stem Cell Research Center, UCLA, Los Angeles, CA, 90095, USA. jli29@vcu.edu.
Yang LiDepartment of Genetics, School of Life Science, Anhui Medical University, Hefei, Anhui, 230031, China. liyang@ahmu.edu.cn.ORCID http://orcid.org/0000-0002-9725-8774
Anhui Medical University · CNFudan University · CNSun Yat-sen University · CNBroad Center · USShenzhen University · CNUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low dose treatment with the DNA methylation inhibitor decitabine has been shown to be applicable for the management of certain types of cancer. However, its antitumor effect and mechanisms are context dependent and its activity has never been systematically studied in bladder cancer treatment. We used mouse models, cultured cell lines and patient-derived xenografts to demonstrate that low dose decitabine treatment remarkably enhanced the effects of cisplatin and gemcitabine on basal-like bladder cancer both in vivo and in vitro. Genetic lineage tracing revealed that the stemness of a bladder cancer stem cell population was inhibited by decitabine treatment in mice. These effects were accompanied by decreases in genome-wide DNA methylation, gene re-expression, and changes in key cellular regulatory pathways such as STAT3 signaling. These results indicate that this DNA-demethylating reagent is a promising therapeutic approach for basal-like bladder cancer treatment.

Indexed as

AnimalsAntimetabolites, AntineoplasticCisplatinDecitabineDeoxycytidineDose-Response Relationship, DrugDrug Therapy, CombinationGemcitabineHumansMaleMiceNeoplastic Stem CellsUrinary Bladder NeoplasmsAntimetabolites, AntineoplasticCisplatinDecitabineDeoxycytidineGemcitabine

Identifiers

PMID30918330
OpenAlexW2922682839

What OpenQuestion holds

Textmetadata
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.