AntiCancer, Inc., San Diego, CA, U.S.A.
Department of Surgery, University of California, San Diego, CA, U.S.A.
Cancer Genomics Proteomics. 2020 May-Jun;17(3):217-223. doi: 10.21873/cgp.20182.
BACKGROUND/AIM: We have previously developed a novel bone-targeting platinum compound, 3Pt, and showed that it has strong inhibitory activity against osteosarcoma cells and orthotopic cell-line xenograft mouse models. In the present report, we compared the efficacy of 3Pt to cisplatinum (CDDP) in a CDDP-resistant relapsed osteosarcoma patient-derived orthotopic xenograft (PDOX) mouse model.
The tumor of a patient with osteosarcoma of the distal femur was treated with CDDP-based chemotherapy followed by surgery. The surgical specimen was used to establish a PDOX model. An osteosarcoma cell line was also established from the original patient tumor. Osteosarcoma cell viability was assessed with the WST-8 assay and the IC50 values were calculated. The PDOX models were randomized into three groups: untreated control, CDDP-treated group, and 3Pt-treated group. Tumor size and body weight were measured twice a week.
3Pt had a strong concentration-dependent cytocidal effect in vitro. The IC value of 3Pt was significantly lower than that of CDDP. On day 14 of the treatment, 3Pt caused a significantly greater tumor growth inhibition compared to the untreated control and CDDP-treated mice.
3Pt is a promising clinical candidate for the treatment of recalcitrant osteosarcoma.
背景/目的:我们之前开发了一种新型的骨靶向铂化合物 3Pt,并表明其对骨肉瘤细胞和原位细胞系异种移植小鼠模型具有很强的抑制活性。在本报告中,我们比较了 3Pt 与顺铂(CDDP)在 CDDP 耐药复发性骨肉瘤患者来源的原位异种移植(PDOX)小鼠模型中的疗效。
接受基于 CDDP 的化疗和手术治疗的远端股骨骨肉瘤患者的肿瘤。手术标本用于建立 PDOX 模型。还从原始患者肿瘤中建立了骨肉瘤细胞系。用 WST-8 法评估骨肉瘤细胞活力,并计算 IC50 值。PDOX 模型随机分为三组:未治疗对照组、CDDP 治疗组和 3Pt 治疗组。每周测量两次肿瘤大小和体重。
3Pt 在体外具有很强的浓度依赖性细胞杀伤作用。3Pt 的 IC 值明显低于 CDDP。在治疗的第 14 天,与未治疗对照组和 CDDP 治疗组相比,3Pt 导致肿瘤生长抑制明显更大。
3Pt 是治疗难治性骨肉瘤的有前途的临床候选药物。