Evidence map›Paper›PMID 31444154›Full record

ArticleCancer research2019

ZBTB7A Mediates the Transcriptional Repression Activity of the Androgen Receptor in Prostate Cancer.

Dong Han, Sujun Chen, Wanting Han, Shuai Gao, Jude N Owiredu, Muqing Li, Steven P Balk, Housheng Hansen He, Changmeng Cai

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 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
2.4field-weighted citation impact, top 10% 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, 36 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

9 authors at 3 institutions in 2 countries.

Dong Han *Center for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts.ORCID 0000-0002-2173-3647
Sujun Chen *Princess Margaret Cancer Center/University Health Network, Toronto, Ontario, Canada.
Wanting Han *Center for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts.ORCID 0000-0002-2173-3647
Shuai GaoCenter for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts.
Jude N OwireduCenter for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts.
Muqing LiCenter for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts.
Steven P BalkBeth Israel Deaconess Medical Center, Boston, Massachusetts.
Housheng Hansen HePrincess Margaret Cancer Center/University Health Network, Toronto, Ontario, Canada. changmeng.cai@umb.edu hansenhe@uhnresearch.ca.
Changmeng CaiCenter for Personalized Cancer Therapy, University of Massachusetts Boston, Boston, Massachusetts. changmeng.cai@umb.edu hansenhe@uhnresearch.ca.
University of Massachusetts Boston · USUniversity of Toronto · CABeth Israel Deaconess Medical Center · US

Funding

Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
Study the Mechanism of Retinoblastoma Protein Mediated Androgen Receptor Transcriptional Repression Activity on DNA ReplicationR01CA211350 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI CAI, CHANGMENG · 2017 to 2021
$1.7M
Molecular basis of androgen receptor mediated gene transcriptional repressionR00CA166507 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI CAI, CHANGMENG · 2015 to 2017
$726k
NCI NIH HHS P01 CA163227NCI NIH HHS R00 CA166507NCI NIH HHS R01 CA211350
6 · The paper itself

Abstract

Loss of expression of context-specific tumor suppressors is a critical event that facilitates the development of prostate cancer. Zinc finger and BTB domain containing transcriptional repressors, such as ZBTB7A and ZBTB16, have been recently identified as tumor suppressors that play important roles in preventing prostate cancer progression. In this study, we used combined ChIP-seq and RNA-seq analyses of prostate cancer cells to identify direct ZBTB7A-repressed genes, which are enriched for transcriptional targets of E2F, and identified that the androgen receptor (AR) played a critical role in the transcriptional suppression of these E2F targets. AR recruitment of the retinoblastoma protein (Rb) was required to strengthen the E2F-Rb transcriptional repression complex. In addition, ZBTB7A was rapidly recruited to the E2F-Rb binding sites by AR and negatively regulated the transcriptional activity of E2F1 on DNA replication genes. Finally, ZBTB7A suppressed the growth of castration-resistant prostate cancer (CRPC)

Indexed as

Transcription, GeneticAdenocarcinomaBinding SitesCell Line, TumorDNA-Binding ProteinsDNA ReplicationE2F1 Transcription FactorHumansMaleNeoplasm ProteinsProstatic NeoplasmsProtein TransportReceptors, AndrogenRecurrenceRetinoblastoma ProteinRNA InterferenceAR protein, humanDNA-Binding ProteinsE2F1 protein, humanE2F1 Transcription FactorNeoplasm ProteinsReceptors, AndrogenRetinoblastoma ProteinTestosteroneTranscription FactorsZBTB7A protein, human

Identifiers

PMID31444154
PMCPMC6801099
OpenAlexW2969441845

What OpenQuestion holds

Textmetadata
LicenceTDM
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.