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sChemNET: a deep learning framework for predicting small molecules targeting microRNA function

delete2024-10-23
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OA
AI
D
Diego Galeano *
I
Imrat
J
Jeffrey Haltom
C
Chaylen Andolino
A
Aliza Yousey
V
Victoria Zaksas
S
Saswati Das
S
Stephen B. Baylin
D
Douglas C. Wallace
F
Frank J. Slack
F
Francisco J. Enguita
E
Eve Syrkin Wurtele
D
Dorothy Teegarden
R
Robert Meller
D
Daniel Cifuentes
A
Afshin Beheshti
DOI:10.1038/s41467-024-49813-wdelete
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Abstract

Abstract

En 中文
MicroRNAs (miRNAs) have been implicated in human disorders, from cancers to infectious diseases. Targeting miRNAs or their target genes with small molecules offers opportunities to modulate dysregulated cellular processes linked to diseases. Yet, predicting small molecules associated with miRNAs remains challenging due to the small size of small molecule-miRNA datasets. Herein, we develop a generalized deep learning framework, sChemNET, for predicting small molecules affecting miRNA bioactivity based on chemical structure and sequence information. sChemNET overcomes the limitation of sparse chemical information by an objective function that allows the neural network to learn chemical space from a large body of chemical structures yet unknown to affect miRNAs. We experimentally validated small molecules predicted to act on miR-451 or its targets and tested their role in erythrocyte maturation during zebrafish embryogenesis. We also tested small molecules targeting the miR-181 network and other miRNAs using in-vitro and in-vivo experiments. We demonstrate that our machine-learning framework can predict bioactive small molecules targeting miRNAs or their targets in humans and other mammalian organisms. Here the authors developed and experimentally validated sChemNET, a deep learning framework to predict small molecules affecting microRNA function based on chemical structure and sequence data. sChemNET predicts bioactive small molecules on the basis of sparse chemical datasets.
Keywords:
NONCODING RNAS
BREAST-CANCER
EXPRESSION
MIGRATION
INVASION
PROLIFERATION
DYSREGULATION
ACTIVATION
CARCINOMA
MIR-451
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Journal

Nature Communications cover
Nature Communications
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15.7
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Citations:
91.2W

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I
indiana university system
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B
boston university
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U
university of pennsylvania
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Harvard Medical School
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pennsylvania medicine
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