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


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.

SUBMITTER: Liu J 

PROVIDER: S-EPMC7001506 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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

Liu Jiwei J   Feng Jingxin J   Li Lili L   Lin Luyao L   Ji Jiafei J   Lin Cong C   Liu Lingxia L   Zhang Na N   Duan Dandan D   Li Zhongwei Z   Huang Baiqu B   Zhang Yu Y   Lu Jun J  

EMBO reports 20191212 2


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  ...[more]

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