雄激素受体功能获得性突变的深度建模。

IF 2.8 4区 医学 Q3 CHEMISTRY, MEDICINAL
Jiaying You, Jane Foo, Nada Lallous, Artem Cherkasov
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引用次数: 0

摘要

雄激素受体(AR)途径抑制剂治疗前列腺癌(PCa)的效率正在下降,原因是人类雄激素受体(AR)发生功能获得性突变等耐药机制。因此,了解和预测这些突变对于制定有效的前列腺癌治疗策略至关重要。利用积累的临床相关AR突变数据和最新的深度建模技术,本研究旨在揭示和量化关键的AR突变与药物之间的关系。通过结合药物和突变基因序列的分子描述符,这项工作将这些特征表示为单一载体,并证明了它们在模拟AR突变对常规抗雄激素的反应方面的有效性。所开发的方法在预测AR突变体的功能获得行为方面达到80%以上的准确率,因此可以潜在地揭示突变药物对之间未知的激动剂/拮抗剂关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Modeling of Gain-of-Function Mutations on Androgen Receptor.

The efficiency of Androgen Receptor (AR) pathway inhibitors for prostate cancer (PCa) is on decline due to resistance mechanisms including the occurrence of gain-of-function mutations on human androgen receptor (AR). Hence, understanding and predicting such mutations is crucial for developing effective PCa treatment strategies. Leveraging accu- mulated data on clinically relevant AR mutants with recent advances in deep modeling techniques, this study aims to unveil and quantify critical AR mutation-drug relation- ships. By incorporating molecular descriptors for drugs and mutated genes sequences, this work represented these features as single vectors and demonstrates their effective- ness in modeling AR mutant responses to conventional antiandrogens. The developed approach achieves above 80% accuracy in predicting the gain-of-function behavior of AR mutants and therefore can potentially uncover unknown agonist/antagonist relationships among mutant-drug pairs.

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来源期刊
Molecular Informatics
Molecular Informatics CHEMISTRY, MEDICINAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.30
自引率
2.80%
发文量
70
审稿时长
3 months
期刊介绍: Molecular Informatics is a peer-reviewed, international forum for publication of high-quality, interdisciplinary research on all molecular aspects of bio/cheminformatics and computer-assisted molecular design. Molecular Informatics succeeded QSAR & Combinatorial Science in 2010. Molecular Informatics presents methodological innovations that will lead to a deeper understanding of ligand-receptor interactions, macromolecular complexes, molecular networks, design concepts and processes that demonstrate how ideas and design concepts lead to molecules with a desired structure or function, preferably including experimental validation. The journal''s scope includes but is not limited to the fields of drug discovery and chemical biology, protein and nucleic acid engineering and design, the design of nanomolecular structures, strategies for modeling of macromolecular assemblies, molecular networks and systems, pharmaco- and chemogenomics, computer-assisted screening strategies, as well as novel technologies for the de novo design of biologically active molecules. As a unique feature Molecular Informatics publishes so-called "Methods Corner" review-type articles which feature important technological concepts and advances within the scope of the journal.
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