Identification and validation of differentially expressed disulfidptosis-related genes in hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is one of the most common cardiovascular diseases with no effective treatment due to its complex pathogenesis. A novel cell death, disulfidptosis, has been extensively studied in the cancer field but rarely in cardiovascular diseases. This study revealed the potential relationship between disulfidptosis and hypertrophic cardiomyopathy and put forward a predictive model containing disulfidptosis-associated genes (DRGs) of GYS1, MYH10, PDMIL1, SLC3A2, CAPZB, showing excellent performance by SVM machine learning model. The results were further validated by western blot, RNA sequencing and immunohistochemistry in a TAC mice model. In addition, resveratrol was selected as a therapeutic drug targeting core genes using the CTD database. In summary, this study provides new perspectives for exploring disulfidptosis-related biomarkers and potential therapeutic targets for hypertrophic cardiomyopathy.

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Publication Details

Journal
Molecular Medicine
Published
2024-12-19
DOI
https://doi.org/10.1186/s10020-024-01024-1
Citations
2
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.47

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article

Identification and validation of differentially expressed disulfidptosis-related genes in hypertrophic cardiomyopathy

Xulong Ding, Yiyao Zeng, Yafeng Zhou, Tong Shao et al.
2 citations
Molecular Medicine
RNA modifications and cancer
0.47
article

Identification and validation of differentially expressed disulfidptosis-related genes in hypertrophic cardiomyopathy

Xulong Ding, Yiyao Zeng, Yafeng Zhou, Tong Shao, Hailong Zhang, Runze Zhao, Xin Tan, Peng Zhou, Huimin Fan, Shuai Xu, Jili Fan, Xiaohong Bo, Yangjun Fu
article en
2 citations

Abstract

Hypertrophic cardiomyopathy (HCM) is one of the most common cardiovascular diseases with no effective treatment due to its complex pathogenesis. A novel cell death, disulfidptosis, has been extensively studied in the cancer field but rarely in cardiovascular diseases. This study revealed the potential relationship between disulfidptosis and hypertrophic cardiomyopathy and put forward a predictive model containing disulfidptosis-associated genes (DRGs) of GYS1, MYH10, PDMIL1, SLC3A2, CAPZB, showing excellent performance by SVM machine learning model. The results were further validated by western blot, RNA sequencing and immunohistochemistry in a TAC mice model. In addition, resveratrol was selected as a therapeutic drug targeting core genes using the CTD database. In summary, this study provides new perspectives for exploring disulfidptosis-related biomarkers and potential therapeutic targets for hypertrophic cardiomyopathy.

Molecular MedicineVol. 30(1)
Soochow University (CN), Second Affiliated Hospital of Soochow University (CN), First Affiliated Hospital of Soochow University (CN), Third People's Hospital of Hefei (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province
Good health and well-being
Openalex Percentile: Top 33%
RNA modifications and cancer
0.47
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