Screening for Synergistic Reagents With Pazopanib Against Osteosarcoma Using a Compound Library

• Published in: Anticancer research Vol. 44; no. 3; p. 1071
• Main Authors: Yada, Yuki, Asanuma, Kunihiro, Kakimto, Takuya, Okuno, Kazuma, Okamoto, Takayuki, Iino, Takahiro, Nakamura, Tomoki, Sudo, Akihiro
• Format: Journal Article
• Language: English
• Published: Greece 01-03-2024
• Subjects: Animals; Apoptosis; Bone Neoplasms - drug therapy; Cell Line, Tumor; Cell Proliferation; Humans; Indazoles - pharmacology; Mice; Osteosarcoma - drug therapy; Proto-Oncogene Proteins c-akt; Pyrimidines; Sulfonamides; ALK; ROS-1; crizotinib; c-KIT; C-Met; Pazopanib; osteosarcoma; platelet-derived growth factor receptor (PDGF); vascular endothelial growth factor receptor (VEGFR)
• ISSN: 1791-7530
• DOI: 10.21873/anticanres.16902

Osteosarcoma (OS) is the most common malignant bone tumor. As the same agents have been in use since the mid-1970s, new therapeutic approaches are needed to improve prognosis. Pazopanib (PZP) has already demonstrated marked antitumor activity clinically and can be effective in patients with metastatic OS. We investigated the combination treatment of candidate agents with PZP and examined effects on tumor growth using an in vivo model.
A library of 324 compounds was used. MG63 OS cells were treated with PZP and each compound. Cell viability was measured. The antiproliferative effects of compound combination on four OS cell lines was tested. Cell signaling was evaluated by western blot analysis. In vivo antitumor testing was performed using 143B-bearing mice.
The screening process identified crizotinib (CRZ) as the most effective drug for combination with PZP. The combination of PZP and CRZ demonstrated effects compared to control or single therapy. Cell signal investigation showed that dual therapy down-regulated c-MYC, p-AKT, p-STAT3, p-cyclin D1 and survivin and up-regulated cleaved caspase-3 and cleaved PARP compared to control or single therapy. In vivo analysis showed dual therapy achieved synergic effects for tumor growth compared to control or single-treatment groups. No significant difference in the change in body weight was observed among groups.
Combined use of PZP and CRZ offers synergic anti-tumor effects against OS, inducing apoptosis in vitro and in vivo by down-regulating AKT and STAT3. Our data suggest that these agents can be used for patients clinically.