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A Chemical Genomics Approach to Drug Reprofiling in Oncology: Antipsychotic Drug Risperidone as a Potential Adenocarcinoma Treatment
- Publication Year :
- 2017
- Publisher :
- Elsevier, 2017.
-
Abstract
- Drug reprofiling is emerging as an effective paradigm for discovery of cancer treatments. Herein, an antipsychotic drug is immobilised using the Magic Tag® chemical genomics tool and screened against a T7 bacteriophage displayed library of polypeptides from Drosophila melanogaster, as a whole genome model, to uncover an interaction with a section of 17-β-HSD10, a proposed prostate cancer target. A computational study and enzyme inhibition assay with full length human 17-β-HSD10 identifies risperidone as a drug reprofiling candidate. When formulated with rumenic acid, risperidone slows proliferation of PC3 prostate cancer cells in vitro and retards PC3 prostate cancer tumour growth in vivo in xenografts in mice, presenting an opportunity to reprofile risperidone as a cancer treatment.
- Subjects :
- Male
0301 basic medicine
Cancer Research
Time Factors
17-Hydroxysteroid Dehydrogenases
Protein Conformation
Pharmacology
Prostate cancer
0302 clinical medicine
Bacteriophage T7
Linoleic Acids, Conjugated
QD
Molecular Targeted Therapy
Enzyme Inhibitors
media_common
3-Hydroxyacyl CoA Dehydrogenases
Genomics
Risperidone
Tumor Burden
Molecular Docking Simulation
Drug repositioning
Drosophila melanogaster
Oncology
030220 oncology & carcinogenesis
Adenocarcinoma
Antipsychotic Agents
medicine.drug
Drug
RM
Drug Compounding
media_common.quotation_subject
Mice, Nude
Antineoplastic Agents
RS
Structure-Activity Relationship
03 medical and health sciences
Cell Line, Tumor
medicine
Animals
Humans
Cell Proliferation
Gene Library
Dose-Response Relationship, Drug
Cell growth
business.industry
Drug Repositioning
Prostatic Neoplasms
Cancer
medicine.disease
Xenograft Model Antitumor Assays
030104 developmental biology
business
Subjects
Details
- Language :
- English
- ISSN :
- 03043835
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....0a0cb2e78f5d86faed414b36368ad130