Evidence map›Paper›PMID 31833203›Full record

ArticleEMBO reports2020

Arginine methylation-dependent LSD1 stability promotes invasion and metastasis of breast cancer.

Jiwei Liu, Jingxin Feng, Lili Li, Luyao Lin, Jiafei Ji, Cong Lin, Lingxia Liu, Na Zhang, Dandan Duan, Zhongwei Li and 3 more

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

79 citing papers in PubMed, 125 citations in OpenAlex.

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19 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 1 country.

Jiwei LiuThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.
Jingxin FengThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.ORCID 0000-0003-0677-2792
Lili LiKey Laboratory of Cancer Prevention and Therapy, Department of Bone and Soft Tissue Oncology, National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Luyao LinThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.
Jiafei JiThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.
Cong LinThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.
Lingxia LiuThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.
Na ZhangThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.
Dandan DuanThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.
Zhongwei LiThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.
Baiqu HuangThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.ORCID 0000-0001-8968-9796
Yu ZhangThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, China.ORCID 0000-0002-3702-6541
Jun LuThe Institute of Genetics and Cytology, Northeast Normal University, Changchun, China.ORCID 0000-0002-9141-6786
Northeast Normal University · CNTianjin Medical University Cancer Institute and Hospital · CN

Funding

National Natural Science Foundation of China 31570718National Natural Science Foundation of China 31571317National Natural Science Foundation of China 31770825National Natural Science Foundation of China 31771335National Natural Science Foundation of China 31870765Science and Technology Development Project of Jilin Province 20180101232JCScience and Technology Development Project of Jilin Province 20180101234JC
6 · The paper itself

Abstract

Histone lysine demethylase 1 (LSD1), the first identified histone demethylase, is overexpressed in multiple tumor types, including breast cancer. However, the mechanisms that cause LSD1 dysregulation in breast cancer remain largely unclear. Here, we report that protein arginine methyltransferase 4 (PRMT4 or CARM1) dimethylates LSD1 at R838, which promotes the binding of the deubiquitinase USP7, resulting in the deubiquitination and stabilization of LSD1. Moreover, CARM1- and USP7-dependent LSD1 stabilization plays a key role in repressing E-cadherin and activating vimentin transcription through promoter H3K4me2 and H3K9me2 demethylation, respectively, which promotes invasion and metastasis of breast cancer cells. Consistently, LSD1 arginine methylation levels correlate with tumor grade in human malignant breast carcinoma samples. Our findings unveil a unique mechanism controlling LSD1 stability by arginine methylation, also highlighting the role of the CARM1-USP7-LSD1 axis in breast cancer progression.

Indexed as

Breast NeoplasmsArginineCell Line, TumorHistone DemethylasesHumansMethylationProtein Processing, Post-TranslationalUbiquitin-Specific Peptidase 7ArginineHistone DemethylasesUbiquitin-Specific Peptidase 7USP7 protein, humanarginine methylationbreast cancerCARM1LSD1metastasis

Identifiers

PMID31833203
PMCPMC7001506
OpenAlexW2996737346

What OpenQuestion holds

Textmetadata
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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.