Evidence map›Paper›PMID 29402932›Full record

ArticleNature communications2018

BMI1 regulates androgen receptor in prostate cancer independently of the polycomb repressive complex 1.

Sen Zhu, Dongyu Zhao, Lin Yan, Weihua Jiang, Jung-Sun Kim, Bingnan Gu, Qipeng Liu, Rui Wang, Bo Xia, Jonathan C Zhao and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Dual-Targeting CSC Therapy: Acid-Responsive Cisplatin/CaCOPharmaceuticals (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. The transcription factor BMI1 increases hypoxic signaling in oral cavity epithelia.Biochimica et biophysica acta. Molecular basis of disease · 2024
    Article
  13. Review
  14. Article
  15. The crosstalk between ubiquitination and endocrine therapy.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Critical Roles of Polycomb Repressive Complexes in Transcription and Cancer.International journal of molecular sciences · 2022
    Review
  20. Review
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

19 authors at 6 institutions in 4 countries.

Sen ZhuCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Dongyu ZhaoCenter for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Lin YanCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Weihua JiangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Jung-Sun KimCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Bingnan GuCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Qipeng LiuCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Rui WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Bo XiaCenter for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Jonathan C ZhaoDivision of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Gang SongDepartment of Urology, Peking University First Hospital, Institute of Urology, Peking University, Beijing, 100034, China.
Wenyi MiDepartment of Epigenetics and Molecular Carcinogenesis, Division of Basic Science Research, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0002-7453-051X
Rong-Fu WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Xiaobing ShiDepartment of Epigenetics and Molecular Carcinogenesis, Division of Basic Science Research, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0001-5242-8189
Hung-Ming LamDepartment of Urology, University of Washington, Seattle, WA, 98195, USA.
Xuesen DongVancouver Prostate Centre, Vancouver General Hospital, Vancouver, BC, V6H 3Z6, Canada.
Jindan YuDivision of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Kaifu ChenCenter for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, TX, 77030, USA. kchen2@houstonmethodist.org.
Qi CaoCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX, 77030, USA. qcao@houstonmethodist.org.ORCID http://orcid.org/0000-0002-5140-3681
Houston Methodist · USNorthwestern University · USThe University of Texas MD Anderson Cancer Center · USMacau University of Science and Technology · MOPeking University · CNUniversity of British Columbia · CA

Funding

The inhibitory network between EZH2 and PARP1 in triple-negative breast cancerR01CA208257 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CAO, QI · 2017 to 2022
$1.8M
Genomics and bioinformatics analysis to understand castration-resistant prostate cancerR50CA211271 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHAO, CHANGSHENG · 2016 to 2020
$701k
NCI NIH HHS R01 CA208257NCI NIH HHS R50 CA211271
6 · The paper itself

Abstract

BMI1, a polycomb group (PcG) protein, plays a critical role in epigenetic regulation of cell differentiation and proliferation, and cancer stem cell self-renewal. BMI1 is upregulated in multiple types of cancer, including prostate cancer. As a key component of polycomb repressive complex 1 (PRC1), BMI1 exerts its oncogenic functions by enhancing the enzymatic activities of RING1B to ubiquitinate histone H2A at lysine 119 and repress gene transcription. Here, we report a PRC1-independent role of BMI1 that is critical for castration-resistant prostate cancer (CRPC) progression. BMI1 binds the androgen receptor (AR) and prevents MDM2-mediated AR protein degradation, resulting in sustained AR signaling in prostate cancer cells. More importantly, we demonstrate that targeting BMI1 effectively inhibits tumor growth of xenografts that have developed resistance to surgical castration and enzalutamide treatment. These results suggest that blocking BMI1 alone or in combination with anti-AR therapy can be more efficient to suppress prostate tumor growth.

Indexed as

AdenocarcinomaAnimalsAntineoplastic Agents, HormonalBenzamidesCell Line, TumorCell ProliferationDisease ProgressionHistonesHumansMaleMiceMice, SCIDNeoplasm TransplantationNitrilesOrchiectomyPhenylthiohydantoinAntineoplastic Agents, HormonalBenzamidesBMI1 protein, humanenzalutamideHistonesMDM2 protein, humanNitrilesPhenylthiohydantoinPolycomb Repressive Complex 1Proto-Oncogene Proteins c-mdm2Receptors, AndrogenRNF2 protein, human

Identifiers

PMID29402932
PMCPMC5799368
OpenAlexW2783562181

What OpenQuestion holds

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Registered trials

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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.