Evidence map›Paper›PMID 29752431›Full record

ArticleCell death & disease2018

DDB2 represses ovarian cancer cell dedifferentiation by suppressing ALDH1A1.

Tiantian Cui, Amit Kumar Srivastava, Chunhua Han, Dayong Wu, Nissar Wani, Lu Liu, Zhiqin Gao, Meihua Qu, Ning Zou, Xiaoli Zhang and 8 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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  9. Article
  10. Targeting ovarian cancer stem cells: a new way out.Stem cell research & therapy · 2023
    Review
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  12. 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

18 authors at 7 institutions in 2 countries.

Tiantian CuiDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Amit Kumar SrivastavaDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Chunhua HanDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Dayong WuDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Nissar WaniDepartment of Pathology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Lu LiuDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Zhiqin GaoDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Meihua QuDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Ning ZouDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Xiaoli ZhangCenter for Biostatistics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Ping YiDepartment of Obstetrics and Gynecology, Daping Hospital, The Third Military Medical University, 40042, Chongqing, China.
Jianhua YuDepartment of Internal Medicine, Division of Hematology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Erica H BellDepartment of Radiation Oncology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Shyh-Ming YangNational Center for Advancing Translational Science, National Institutes of Health, Rockville, MD, 20850, USA.
David J MaloneyNational Center for Advancing Translational Science, National Institutes of Health, Rockville, MD, 20850, USA.
Yanfang ZhengOncology Center, Zhujiang Hospital, Southern Medical University, 510282, Guangdong, Guangzhou, China.
Altaf A WaniDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Qi-En WangDepartment of Radiology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA. wang.771@osu.edu.
The Ohio State University · USWeifang Medical University · CNZhujiang Hospital · CNDaping Hospital · CNHubei Cancer Hospital · CNNational Center for Advancing Translational Sciences · USNational Institutes of Health · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
Averting recurrent and resistant ovarian tumorsR01CA211175 · NCI · OHIO STATE UNIVERSITY · PI WANG, QIEN · 2017 to 2021
$2.3M
Overcoming Barriers of Virotherapy by Next-Generation oHSV Expressing E-CadherinR01NS106170 · NINDS · OHIO STATE UNIVERSITY · PI YU, JIANHUA · 2018 to 2023
$1.9M
Role of DDB2 in chemotherapeutic agents-induced apoptosis and platinum resistanceR01CA151248 · NCI · OHIO STATE UNIVERSITY · PI WANG, QIEN · 2011 to 2014
$990k
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA151248NCI NIH HHS R01 CA211175NINDS NIH HHS R01 NS106170
6 · The paper itself

Abstract

Cancer stem cells (CSCs), representing the root of many solid tumors including ovarian cancer, have been implicated in disease recurrence, metastasis, and therapeutic resistance. Our previous study has demonstrated that the CSC subpopulation in ovarian cancer can be limited by DNA damage-binding protein 2 (DDB2). Here, we demonstrated that the ovarian CSC subpopulation can be maintained via cancer cell dedifferentiation, and DDB2 is able to suppress this non-CSC-to-CSC conversion by repression of ALDH1A1 transcription. Mechanistically, DDB2 binds to the ALDH1A1 gene promoter, facilitating the enrichment of histone H3K27me3, and competing with the transcription factor C/EBPβ for binding to this region, eventually inhibiting the promoter activity of the ALDH1A1 gene. The de-repression of ALDH1A1 expression contributes to DDB2 silencing-augmented non-CSC-to-CSC conversion and expansion of the CSC subpopulation. We further showed that treatment with a selective ALDH1A1 inhibitor blocked DDB2 silencing-induced expansion of CSCs, and halted orthotopic xenograft tumor growth. Together, our data demonstrate that DDB2, functioning as a transcription repressor, can abrogate ovarian CSC properties by downregulating ALDH1A1 expression.

Indexed as

Cell DedifferentiationGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGene SilencingAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyCell Line, TumorDNA-Binding ProteinsFemaleHumansNeoplasm ProteinsNeoplastic Stem CellsOvarian NeoplasmsPromoter Regions, GeneticRetinal DehydrogenaseAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, humanDDB2 protein, humanDNA-Binding ProteinsNeoplasm ProteinsRetinal Dehydrogenase

Identifiers

PMID29752431
PMCPMC5948213
OpenAlexW2801001438

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.