Evidence map›Paper›PMID 31636385›Full record

ArticleOncogene2020

HNF1B-mediated repression of SLUG is suppressed by EZH2 in aggressive prostate cancer.

Jianqing Wang, Chenxi He, Peng Gao, Siqing Wang, Ruitu Lv, Huihui Zhou, Qidong Zhou, Ke Zhang, Jian Sun, Caibin Fan and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 47 citations in OpenAlex.

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  19. Critical Roles of Polycomb Repressive Complexes in Transcription and Cancer.International journal of molecular sciences · 2022
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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

12 authors at 3 institutions in 3 countries.

Jianqing Wang *Department of Urology, The Affiliated Suzhou Hospital of Nanjing Medical University, 215002, Suzhou, Jiangsu, China. jqwang14@fudan.edu.cn.ORCID http://orcid.org/0000-0002-0709-9694
Chenxi He *Key Laboratory of Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Liver Cancer Institute, Zhongshan Hospital, Fudan University, 200032, Shanghai, China.
Peng Gao *Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Siqing WangKey Laboratory of Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Liver Cancer Institute, Zhongshan Hospital, Fudan University, 200032, Shanghai, China.
Ruitu LvKey Laboratory of Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Liver Cancer Institute, Zhongshan Hospital, Fudan University, 200032, Shanghai, China.
Huihui ZhouDepartment of pathology, Affiliated Yuhuangding Hospital of Qingdao University, 266071, Shandong, China.
Qidong ZhouDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Ke ZhangDepartment of Urology, The Affiliated Suzhou Hospital of Nanjing Medical University, 215002, Suzhou, Jiangsu, China.
Jian SunDepartment of Urology, The Affiliated Suzhou Hospital of Nanjing Medical University, 215002, Suzhou, Jiangsu, China.
Caibin FanDepartment of Urology, The Affiliated Suzhou Hospital of Nanjing Medical University, 215002, Suzhou, Jiangsu, China.
Guanxiong DingDepartment of Urology, Huashan Hospital, Fudan University, Shanghai, China. dingguanxiong1981@126.com.
Fei LanKey Laboratory of Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Liver Cancer Institute, Zhongshan Hospital, Fudan University, 200032, Shanghai, China. fei_lan@fudan.edu.cn.
Fudan University · CNSuzhou Municipal Hospital · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer is the most common malignancy in men in developed countries. Overexpression of enhancer of zeste homolog 2 (EZH2), the major histone H3 lysine 27 methyltransferase, has been connected to prostate cancer malignancy. However, its downstream genes and pathways have not been well established. Here, we show tumor suppressor Hepatocyte Nuclear Factor 1β (HNF1B) as a direct downstream target of EZH2. EZH2 binds HNF1B locus and suppresses HNF1B expression in prostate cancer cell lines, which is further supported by the reverse correlation between EZH2 and HNF1B expression in clinical samples. Consistently, restored HNF1B expression significantly suppresses EZH2-mediated overgrowth and EMT processes, including migration and invasion of prostate cancer cell lines. Mechanistically, we find that HNF1B primarily binds the promoters of thousands of target genes, and differentially regulates the expression of 876 genes. We also identify RBBP7/RbAP46 as a HNF1B interacting protein which is required for HNF1B-mediated repression of SLUG expression and EMT process. Importantly, we find that higher HNF1B expression strongly predicts better prognosis of prostate cancer, alone or together with lower EZH2 expression. Taken together, we have established a previously underappreciated axis of EZH2-HNF1B-SLUG in prostate cancer, and also provide evidence supporting HNF1B as a potential prognosis marker for metastatic prostate cancer.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorCell MovementCell ProliferationEnhancer of Zeste Homolog 2 ProteinHepatocyte Nuclear Factor 1-betaHumansMalePrognosisPromoter Regions, GeneticProstatic NeoplasmsSnail Family Transcription FactorsTumor Cells, CulturedBiomarkers, TumorEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHepatocyte Nuclear Factor 1-betaHNF1B protein, humanSNAI1 protein, humanSnail Family Transcription Factors

Identifiers

PMID31636385
PMCPMC7002300
OpenAlexW2980574182

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.