Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma

Ferroptosis is a newly characterized form of iron-dependent non-apoptotic cell death, which is closely associated with cancer progression. However, the functions and mechanisms in regulation of escaping from ferroptosis during hepatocellular carcinoma (HCC) progression remain unknown. In this study,...

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Main Authors: Hang Zhai, Sisi Zhong, Runxin Wu, Zhaohong Mo, Shiyang Zheng, Jinhua Xue, Hongyu Meng, Maosheng Liu, Xianyu Chen, Guangquan Zhang, Xiyan Zheng, Fei Du, Ruixi Li, Boxuan Zhou
Format: Article
Language:English
Published: Taylor & Francis Group 2023-12-01
Series:Epigenetics
Subjects:
Online Access:http://dx.doi.org/10.1080/15592294.2023.2192438
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author Hang Zhai
Sisi Zhong
Runxin Wu
Zhaohong Mo
Shiyang Zheng
Jinhua Xue
Hongyu Meng
Maosheng Liu
Xianyu Chen
Guangquan Zhang
Xiyan Zheng
Fei Du
Ruixi Li
Boxuan Zhou
author_facet Hang Zhai
Sisi Zhong
Runxin Wu
Zhaohong Mo
Shiyang Zheng
Jinhua Xue
Hongyu Meng
Maosheng Liu
Xianyu Chen
Guangquan Zhang
Xiyan Zheng
Fei Du
Ruixi Li
Boxuan Zhou
author_sort Hang Zhai
collection DOAJ
description Ferroptosis is a newly characterized form of iron-dependent non-apoptotic cell death, which is closely associated with cancer progression. However, the functions and mechanisms in regulation of escaping from ferroptosis during hepatocellular carcinoma (HCC) progression remain unknown. In this study, we reported that the RNA binding motif single stranded interacting protein 1 (RBMS1) participated in HCC development,and functioned as a regulator of ferroptosis. Clinically, the downregulation of RBMS1 occurred in HCC tissues, and low RBMS1 expression was associated with worse HCC patients survival. Mechanistically, RBMS1 overexpression inhibited HCC cell growth by attenuating the expression of glutathione peroxidase 4 (GPX4)and further facilitated ferroptosis in vitro and in vivo. More importantly, a novel circIDE (hsa_circ_0000251) was identified to elevate RBMS1 expression via sponging miR-19b-3p in HCC cells. Collectively, our findings established circIDE/miR-19b-3p/RBMS1 axis as a regulator of ferroptosis, which could be a promising therapeutic target and prognostic factor.
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spelling doaj.art-5b4b6bcfd6724c0abf96217f2db533422023-09-21T13:23:13ZengTaylor & Francis GroupEpigenetics1559-22941559-23082023-12-0118110.1080/15592294.2023.21924382192438Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinomaHang Zhai0Sisi Zhong1Runxin Wu2Zhaohong Mo3Shiyang Zheng4Jinhua Xue5Hongyu Meng6Maosheng Liu7Xianyu Chen8Guangquan Zhang9Xiyan Zheng10Fei Du11Ruixi Li12Boxuan Zhou13The First Affiliated Hospital of Gannan Medical UniversityThe First Affiliated Hospital of Gannan Medical UniversitySun Yat-sen UniversitySun Yat-sen UniversityCancer Center of Guangzhou Medical Universitythe School of Basic Medical Sciences of Gannan Medical UniversitySun Yat-sen Universitythe First Affiliated Hospital of Gannan Medical UniversitySun Yat-sen UniversitySun Yat-sen UniversitySun Yat-sen UniversitySun Yat-sen UniversitySun Yat-sen UniversitySun Yat-sen UniversityFerroptosis is a newly characterized form of iron-dependent non-apoptotic cell death, which is closely associated with cancer progression. However, the functions and mechanisms in regulation of escaping from ferroptosis during hepatocellular carcinoma (HCC) progression remain unknown. In this study, we reported that the RNA binding motif single stranded interacting protein 1 (RBMS1) participated in HCC development,and functioned as a regulator of ferroptosis. Clinically, the downregulation of RBMS1 occurred in HCC tissues, and low RBMS1 expression was associated with worse HCC patients survival. Mechanistically, RBMS1 overexpression inhibited HCC cell growth by attenuating the expression of glutathione peroxidase 4 (GPX4)and further facilitated ferroptosis in vitro and in vivo. More importantly, a novel circIDE (hsa_circ_0000251) was identified to elevate RBMS1 expression via sponging miR-19b-3p in HCC cells. Collectively, our findings established circIDE/miR-19b-3p/RBMS1 axis as a regulator of ferroptosis, which could be a promising therapeutic target and prognostic factor.http://dx.doi.org/10.1080/15592294.2023.2192438circrnaferroptosisrna binding protein
spellingShingle Hang Zhai
Sisi Zhong
Runxin Wu
Zhaohong Mo
Shiyang Zheng
Jinhua Xue
Hongyu Meng
Maosheng Liu
Xianyu Chen
Guangquan Zhang
Xiyan Zheng
Fei Du
Ruixi Li
Boxuan Zhou
Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
Epigenetics
circrna
ferroptosis
rna binding protein
title Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
title_full Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
title_fullStr Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
title_full_unstemmed Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
title_short Suppressing circIDE/miR-19b-3p/RBMS1 axis exhibits promoting-tumour activity through upregulating GPX4 to diminish ferroptosis in hepatocellular carcinoma
title_sort suppressing circide mir 19b 3p rbms1 axis exhibits promoting tumour activity through upregulating gpx4 to diminish ferroptosis in hepatocellular carcinoma
topic circrna
ferroptosis
rna binding protein
url http://dx.doi.org/10.1080/15592294.2023.2192438
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