Screening FDA-Approved Oncology Drugs with Three-Dimensional Spheroids Identifies Romidepsin as a Therapeutic Candidate for Osteosarcoma
Year: 2025
Type: article
Abstract: Osteosarcoma is the most common primary malignant bone tumor and predominantly affects adolescents and young adults. It is the third most common cause of cancer-related deaths among 9 to 24 year olds. Despite aggressive chemotherapeutic and surgical therapies, the survival rate is only 25% for patients with detectable lung metastases at diagnosis and only 70% in patients who present without detectable lung metastases. The poor prognosis is due to growth of metastases irrespective of whether they are initially large enough to detect clinically. It is therefore necessary to develop new methods to target the growth of lung micrometastases. An NCI panel of FDA-approved oncology drugs was therefore screened using three highly metastatic human osteosarcoma cell lines. To more closely approximate in vivo micrometastases, the screen used a three-dimensional multicellular in vitro osteosarcoma spheroid (sarcosphere) model. Among 13 hits from the initial screen, we identified the histone deacetylase inhibitor (HDI) romidepsin as the most promising inhibitor in secondary screens comparing effects on sarcospheres with clinically achievable levels and to effects on non-transformed cells. Romidepsin potency was evident with and without standard-of-care chemotherapeutics (MAP: methotrexate, adriamycin, and cisplatin) at romidepsin concentrations that are clinically achievable and did not affect non-transformed cells. Romidepsin also substantially outperformed the other three FDA-approved HDIs and eight HDIs in clinical trials. The effects of romidepsin were a transient cell cycle block at G2/M and cell death. Importantly, sarcospheres derived from ∼30% of human and 50% of canine patient samples responded to romidepsin at clinically tolerable concentrations (ED50s <70 nmol/L). SIGNIFICANCE: Our unbiased sarcosphere-based drug screen identified romidepsin as a promising candidate to repurpose for human and canine patients with metastatic osteosarcoma. This screening strategy allowed us to identify romidepsin-sensitive and -resistant patients. Sarcosphere-based screening may therefore be useful to identify patients most likely to respond clinically to romidepsin or other drugs.
Source: Cancer Research Communications
Authors: Emily E. Seiden, Spencer M. Richardson, Leah A. Everitt, Gabrielle J. Knafler, Alyssa L. Walker, Venetia A. Whiteside, Divya Pillutla, Shrey Ramnath, Gavin P. Kinsella, Piper A. Wilburn, James D. Buschbach, Deep A. Gandhi, M. Reza Saadatzadeh, L. Daniel Wurtz, Patrick J. Getty, Sheldon L. Padgett, Rance M. Gamblin, Michael O. Childress, Christopher M. Fulkerson, Maegan L. Capitano, Karen E. Pollok, Christopher D. Collier, Edward M. Greenfield
Institutions: Indiana University Indianapolis, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indiana University School of Medicine, University Hospitals of Cleveland, University Hospitals Cleveland Medical Center, Case Western Reserve University, Purdue University West Lafayette, Purdue University Institute for Cancer Research
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,550
Funders: U.S. Department of Defense, Orthopaedic Research and Education Foundation, Rally Foundation, International Max Planck Research School for Advanced Methods in Process and Systems Engineering, Scheme for Promotion of Academic and Research Collaboration, National Institutes of Health, Centers for Disease Control and Prevention, University of Texas MD Anderson Cancer Center, School of Medicine, Indiana University, Melvin and Bren Simon Cancer Center, Indiana University, National Cancer Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Center for Advancing Translational Sciences
Awards: G1628476732, G19765052, G2329068560, G556919504, G569920907, G7321284031, G8662318106, G9000025480, G9000212862, Comprehensive Musculoskeletal Training Program, Indiana Clinical and Translational Sciences Institute, Pediatric and Adult Translational Cancer Drug Discovery and Development Training Program (PACT-D3)
OpenAlex ID: W4414199713
