1. Computational Drug Repositioning Identifies Potentially Active Therapies for Chordoma
- Author
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Shaan M. Raza, Visweswaran Ravikumar, Hadley E. Sheppard, Jonathan D. Breshears, Shreyaskumar Patel, Jeffrey I. Traylor, Charles Y. Lin, and Franco DeMonte
- Subjects
musculoskeletal diseases ,medicine.medical_treatment ,Antineoplastic Agents ,Bone Neoplasms ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Chordoma ,Animals ,Humans ,Medicine ,Computer Simulation ,030304 developmental biology ,0303 health sciences ,Chemotherapy ,business.industry ,Venetoclax ,Drug Repositioning ,medicine.disease ,Skull Base Chordoma ,Drug repositioning ,chemistry ,030220 oncology & carcinogenesis ,Pharmacogenomics ,Cancer research ,Cytarabine ,Surgery ,Neurology (clinical) ,business ,Toxicogenomics ,medicine.drug - Abstract
Background Chordomas are aggressive bone tumors that often recur despite maximal resection and adjuvant radiation. To date there are no Food and Drug Administration (FDA)-approved chemotherapies. Computational drug repositioning is an expanding approach to identify pharmacotherapies for clinical trials. Objective To identify FDA-approved compounds for repurposing in chordoma. Methods Previously identified highly differentially expressed genes from chordoma tissue samples at our institution were compared with pharmacogenomic interactions in the Comparative Toxicogenomics Database (CTD) using ksRepo, a drug-repositioning platform. Compounds selected by ksRepo were then validated in CH22 and UM-Chor1 human chordoma cells in Vitro. Results A total of 13 chemical compounds were identified in silico from the CTD, and 6 were selected for preclinical validation in human chordoma cell lines based on their clinical relevance. Of these, 3 identified drugs are FDA-approved chemotherapies for other malignancies (cisplatin, cytarabine, and lucanthone). Cytarabine, a deoxyribonucleic acid polymerase inhibitor approved for the treatment of various leukemias, exhibited a significant concentration-dependent effect against CH22 and UM-Chor1 cells when compared to positive (THZ1) and negative (venetoclax) controls. Tretinoin exhibited a significant concentration-dependent cytotoxic effect in CH22, sacral chordoma-derived cell lines but to a much lesser extent in UM-Chor1, a cell line derived from skull base chordoma. Conclusion Cytarabine administration reduces the viability of human chordoma cells. The equally effective reduction in viability seen with tretinoin seems to be cell line dependent. Based on our findings, we recommend the evaluation of cytarabine and tretinoin in an expanded set of human chordoma cell lines and animal models.
- Published
- 2020