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<p>CryAB, known as Alpha-B Crystallin, has also been shown to bind and increase the unfolding force of the filamentous protein. Mutation of <i>CryAB</i> at R120G causes serious cardiomyopathy but lacks ideal therapeutic drugs. In the present study, we constructed <i>CryAB</i> (R120G)-transgenic (TG) mice. One hundred and four differentially expressed genes (DEGs) in heart tissues of TG mice were screened through RNA sequencing. Gene ontology (GO) and KEGG pathway analyses highlighted enrichment in critical biological processes such as blood circulation regulation, contractile fiber formation, actin binding, thyroid hormone signaling, endocytosis, and alanine, aspartate, and glutamate metabolism. Protein-protein interaction (PPI) analysis pinpointed key hub genes, including DHTKD1, NKTR, SCN5A, CLCN1, RPA1, ACSF2, ACACB, TTC28, HSPA1B. By using Connectivity Map (CMap) analysis and transcriptome data, we identified phosphodiesterase (PDE) family as potential targets and several potential therapeutic candidates, with nortriptyline, torin-1, and cilostazol emerging as top candidates. Molecular docking simulations showed that Nortriptyline exhibited strong binding affinities with hub proteins, particularly SCN5A. These findings suggest promising new therapeutic strategies for CryAB(R120G)-related cardiomyopathy by targeting specific pathways and hub genes to mitigate cardiac dysfunction.</p>

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Comprehensive bioinformatic analysis identifies potential therapeutic drugs for CryAB (R120G)-related cardiomyopathy

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月30日

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  • Jiaqi Zheng,
  • Yuyang Liu,
  • Jie Wang,
  • Jiajia Hu,
  • Wei Qiu,
  • Ming Su

摘要

CryAB, known as Alpha-B Crystallin, has also been shown to bind and increase the unfolding force of the filamentous protein. Mutation of CryAB at R120G causes serious cardiomyopathy but lacks ideal therapeutic drugs. In the present study, we constructed CryAB (R120G)-transgenic (TG) mice. One hundred and four differentially expressed genes (DEGs) in heart tissues of TG mice were screened through RNA sequencing. Gene ontology (GO) and KEGG pathway analyses highlighted enrichment in critical biological processes such as blood circulation regulation, contractile fiber formation, actin binding, thyroid hormone signaling, endocytosis, and alanine, aspartate, and glutamate metabolism. Protein-protein interaction (PPI) analysis pinpointed key hub genes, including DHTKD1, NKTR, SCN5A, CLCN1, RPA1, ACSF2, ACACB, TTC28, HSPA1B. By using Connectivity Map (CMap) analysis and transcriptome data, we identified phosphodiesterase (PDE) family as potential targets and several potential therapeutic candidates, with nortriptyline, torin-1, and cilostazol emerging as top candidates. Molecular docking simulations showed that Nortriptyline exhibited strong binding affinities with hub proteins, particularly SCN5A. These findings suggest promising new therapeutic strategies for CryAB(R120G)-related cardiomyopathy by targeting specific pathways and hub genes to mitigate cardiac dysfunction.