SSL-VQ: vector-quantized variational autoencoders for semi-supervised prediction of therapeutic targets across diverse diseases

Motivation Identifying effective therapeutic targets poses a challenge in drug discovery, especially for uncharacterized diseases without known therapeutic targets (e.g. rare diseases, intractable diseases). Results This study presents a novel machine learning approach using multimodal vector-quanti...

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Vydáno v:Bioinformatics (Oxford, England) Ročník 41; číslo 2
Hlavní autoři: Namba, Satoko, Li, Chen, Yuyama Otani, Noriko, Yamanishi, Yoshihiro
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Oxford University Press 04.02.2025
Témata:
Autoencoder
Computational Biology - methods
Disease - genetics
Drug Discovery - methods
Humans
Original Paper
Supervised Machine Learning
ISSN:1367-4811, 1367-4803, 1367-4811
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Shrnutí:Motivation Identifying effective therapeutic targets poses a challenge in drug discovery, especially for uncharacterized diseases without known therapeutic targets (e.g. rare diseases, intractable diseases). Results This study presents a novel machine learning approach using multimodal vector-quantized variational autoencoders (VQ-VAEs) for predicting therapeutic target molecules across diseases. To address the lack of known therapeutic target–disease associations, we incorporate the information on uncharacterized diseases without known targets or uncharacterized proteins without known indications (applicable diseases) in the semi-supervised learning (SSL) framework. The method integrates disease-specific and protein perturbation profiles with genetic perturbations (e.g. gene knockdowns and gene overexpressions) at the transcriptome level. Cross-cell representation learning, facilitated by VQ-VAEs, was performed to extract informative features from protein perturbation profiles across diverse human cell types. Concurrently, cross-disease representation learning was performed, leveraging VQ-VAE, to extract informative features reflecting disease states from disease-specific profiles. The model’s applicability to uncharacterized diseases or proteins is enhanced by considering the consistency between disease-specific and patient-specific signatures. The efficacy of the method is demonstrated across three practical scenarios for 79 diseases: target repositioning for target–disease pairs, new target prediction for uncharacterized diseases, and new indication prediction for uncharacterized proteins. This method is expected to be valuable for identifying therapeutic targets across various diseases. Availability and implementation Code: github.com/YamanishiLab/SSL-VQ and Data: 10.5281/zenodo.14644837.
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ISSN:1367-4811
1367-4803
1367-4811
DOI:10.1093/bioinformatics/btaf039