Identification of PIK3CG and SYK as Dual Therapeutic Targets in Parkinson's Disease Microglia via Single-Cell RNA Sequencing and Computational Drug Repurposing

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Autori principali: Ritschel, Glen Charles, Claude
Natura: Recurso digital
Pubblicazione: Zenodo 2026
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author Ritschel, Glen Charles
Claude
author_facet Ritschel, Glen Charles
Claude
contents <p>Provisional patent specification filed with the United States Patent and Trademark Office (USPTO) by Glen Charles Ritschel, Ritschel Research, Tega Cay, South Carolina (Micro-Entity; Application # 64/015,045; filed March 24, 2026). This specification discloses a computational drug repurposing method applied to single-cell RNA sequencing data from Parkinson's Disease patient substantia nigra (GSE157783; Smajić et al., Brain 2022; 40,452 cells; 11 PD donors). A single dominant microglial cluster (cluster 3; P2RY12⁺, CX3CR1⁺, CSF1R⁺) was identified, and differential expression analysis yielded 2,638 microglial-enriched genes. Seven ChEMBL-tractable targets were extracted (SYK, PIK3CG, CD86, CSF3R, CLEC7A, PTPRC, CX3CR1), and 8,793 unique compounds were screened and verified as NOVEL_ALL by USPTO prior art search. Top dual-target PIK3CG/SYK leads include APITOLISIB (CHEMBL1922094; final score 58.8), LESTAURTINIB (CHEMBL603469; 58.0), and FEDRATINIB (CHEMBL1287853; 42.8). A cross-disease SYK convergence signal was identified between this Parkinson's Disease dataset and an independent Alzheimer's Disease microglial dataset. Pipeline code: <a href="https://github.com/glenritschel/parkinsons-scrna">https://github.com/glenritschel/parkinsons-scrna</a></p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_19210175
institution Zenodo
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publishDate 2026
publisher Zenodo
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spellingShingle Identification of PIK3CG and SYK as Dual Therapeutic Targets in Parkinson's Disease Microglia via Single-Cell RNA Sequencing and Computational Drug Repurposing
Ritschel, Glen Charles
Claude
Parkinson's Disease
microglia
scRNA-seq
single-cell RNA sequencing
drug repurposing
PIK3CG
SYK
kinase inhibitor
neuroinflammation
substantia nigra
APITOLISIB
LESTAURTINIB
FEDRATINIB
computational biology
provisional patent
USPTO
ChEMBL
GSE157783
Ritschel Research
<p>Provisional patent specification filed with the United States Patent and Trademark Office (USPTO) by Glen Charles Ritschel, Ritschel Research, Tega Cay, South Carolina (Micro-Entity; Application # 64/015,045; filed March 24, 2026). This specification discloses a computational drug repurposing method applied to single-cell RNA sequencing data from Parkinson's Disease patient substantia nigra (GSE157783; Smajić et al., Brain 2022; 40,452 cells; 11 PD donors). A single dominant microglial cluster (cluster 3; P2RY12⁺, CX3CR1⁺, CSF1R⁺) was identified, and differential expression analysis yielded 2,638 microglial-enriched genes. Seven ChEMBL-tractable targets were extracted (SYK, PIK3CG, CD86, CSF3R, CLEC7A, PTPRC, CX3CR1), and 8,793 unique compounds were screened and verified as NOVEL_ALL by USPTO prior art search. Top dual-target PIK3CG/SYK leads include APITOLISIB (CHEMBL1922094; final score 58.8), LESTAURTINIB (CHEMBL603469; 58.0), and FEDRATINIB (CHEMBL1287853; 42.8). A cross-disease SYK convergence signal was identified between this Parkinson's Disease dataset and an independent Alzheimer's Disease microglial dataset. Pipeline code: <a href="https://github.com/glenritschel/parkinsons-scrna">https://github.com/glenritschel/parkinsons-scrna</a></p>
title Identification of PIK3CG and SYK as Dual Therapeutic Targets in Parkinson's Disease Microglia via Single-Cell RNA Sequencing and Computational Drug Repurposing
topic Parkinson's Disease
microglia
scRNA-seq
single-cell RNA sequencing
drug repurposing
PIK3CG
SYK
kinase inhibitor
neuroinflammation
substantia nigra
APITOLISIB
LESTAURTINIB
FEDRATINIB
computational biology
provisional patent
USPTO
ChEMBL
GSE157783
Ritschel Research
url https://doi.org/10.5281/zenodo.19210175