ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells

Abstract Identifying novel targets for molecular radiosensitization is critical for improving the efficacy of colorectal cancer (CRC) radiotherapy. Alpha-thalassemia/mental retardation X-linked (ATRX), a member of the SWI/SNF-like chromatin remodeling protein family, functions in the maintenance of...

Full description

Saved in:
Bibliographic Details
Main Authors: Lijing Qin, Geng Tang, Ruirui Gui, Yanming Yang, Li Wang, Weiqiang Xu, Hongyuan Tian, Lei Yu, Xiangshan Yang, Zhicheng Wang
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-024-85085-6
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841559741752410112
author Lijing Qin
Geng Tang
Ruirui Gui
Yanming Yang
Li Wang
Weiqiang Xu
Hongyuan Tian
Lei Yu
Xiangshan Yang
Zhicheng Wang
author_facet Lijing Qin
Geng Tang
Ruirui Gui
Yanming Yang
Li Wang
Weiqiang Xu
Hongyuan Tian
Lei Yu
Xiangshan Yang
Zhicheng Wang
author_sort Lijing Qin
collection DOAJ
description Abstract Identifying novel targets for molecular radiosensitization is critical for improving the efficacy of colorectal cancer (CRC) radiotherapy. Alpha-thalassemia/mental retardation X-linked (ATRX), a member of the SWI/SNF-like chromatin remodeling protein family, functions in the maintenance of genomic integrity and the regulation of apoptosis and senescence. However, whether ATRX is directly involved in the radiosensitivity of CRC remains unclear. Our results showed that silencing ATRX increased the radiosensitivity of HCT116 CRC cells, which was further strengthened when p53 was depleted. To explore the potential mechanism, we focused on the impact of the ionizing radiation (IR)-induced DNA damage response (DDR), apoptosis, and senescence and the activation of the Daxx/MDM2/p53 pathway caused by ATRX loss. The results showed that IR induced DNA damage and G2/M arrest after depleting ATRX, especially in p53-depleted HCT116 cells, and inhibited ATM/Chk2 pathway activation, indicating that ATRX loss leads to failure of triggering the ATM/Chk2 pathway. Accordingly, ATRX loss promotes cell apoptosis and attenuates cell senescence. Interestingly, our results indicate that ATRX loss upregulates p53 function via the Daxx/MDM2 pathway to mediate radiosensitivity. Thus, ATRX may represent a novel radiosensitizing target for CRC, particularly p53-deficient CRC.
format Article
id doaj-art-718fa7dcfdf1403794054d628faade76
institution Kabale University
issn 2045-2322
language English
publishDate 2025-01-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-718fa7dcfdf1403794054d628faade762025-01-05T12:16:01ZengNature PortfolioScientific Reports2045-23222025-01-0115111110.1038/s41598-024-85085-6ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cellsLijing Qin0Geng Tang1Ruirui Gui2Yanming Yang3Li Wang4Weiqiang Xu5Hongyuan Tian6Lei Yu7Xiangshan Yang8Zhicheng Wang9NHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityDepartment of Radiotherapy, Second hospital of Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityDepartment of Radiotherapy, Second hospital of Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityNHC Key Laboratory of Radiobiology (Jilin University), School of Public Health, Jilin UniversityAbstract Identifying novel targets for molecular radiosensitization is critical for improving the efficacy of colorectal cancer (CRC) radiotherapy. Alpha-thalassemia/mental retardation X-linked (ATRX), a member of the SWI/SNF-like chromatin remodeling protein family, functions in the maintenance of genomic integrity and the regulation of apoptosis and senescence. However, whether ATRX is directly involved in the radiosensitivity of CRC remains unclear. Our results showed that silencing ATRX increased the radiosensitivity of HCT116 CRC cells, which was further strengthened when p53 was depleted. To explore the potential mechanism, we focused on the impact of the ionizing radiation (IR)-induced DNA damage response (DDR), apoptosis, and senescence and the activation of the Daxx/MDM2/p53 pathway caused by ATRX loss. The results showed that IR induced DNA damage and G2/M arrest after depleting ATRX, especially in p53-depleted HCT116 cells, and inhibited ATM/Chk2 pathway activation, indicating that ATRX loss leads to failure of triggering the ATM/Chk2 pathway. Accordingly, ATRX loss promotes cell apoptosis and attenuates cell senescence. Interestingly, our results indicate that ATRX loss upregulates p53 function via the Daxx/MDM2 pathway to mediate radiosensitivity. Thus, ATRX may represent a novel radiosensitizing target for CRC, particularly p53-deficient CRC.https://doi.org/10.1038/s41598-024-85085-6ATRXRadiosensitivityDNA damage responseDaxx/MDM2/p53 pathwayColorectal cancer
spellingShingle Lijing Qin
Geng Tang
Ruirui Gui
Yanming Yang
Li Wang
Weiqiang Xu
Hongyuan Tian
Lei Yu
Xiangshan Yang
Zhicheng Wang
ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
Scientific Reports
ATRX
Radiosensitivity
DNA damage response
Daxx/MDM2/p53 pathway
Colorectal cancer
title ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
title_full ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
title_fullStr ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
title_full_unstemmed ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
title_short ATRX loss inhibits DDR to strengthen radio-sensitization in p53-deficent HCT116 cells
title_sort atrx loss inhibits ddr to strengthen radio sensitization in p53 deficent hct116 cells
topic ATRX
Radiosensitivity
DNA damage response
Daxx/MDM2/p53 pathway
Colorectal cancer
url https://doi.org/10.1038/s41598-024-85085-6
work_keys_str_mv AT lijingqin atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT gengtang atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT ruiruigui atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT yanmingyang atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT liwang atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT weiqiangxu atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT hongyuantian atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT leiyu atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT xiangshanyang atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells
AT zhichengwang atrxlossinhibitsddrtostrengthenradiosensitizationinp53deficenthct116cells