Department of Orthopedic Surgery, Chiba Cancer Center, Chiba, Japan;
Laboratory of Oncogenomics, Chiba Cancer Center Research Institute, Chiba, Japan.
Anticancer Res. 2024 Mar;44(3):1045-1049. doi: 10.21873/anticanres.16899.
BACKGROUND/AIM: Osteosarcoma (OS) is a rare malignant tumor with a poor survival rate. Our previous study reported that auranofin (AUR), a thioredoxin reductase inhibitor, suppresses OS pulmonary metastases; however, the local progression of OS is not affected, in vivo. Nonetheless, the development of augmentation therapy with AUR to inhibit OS local progression remains challenging. Celecoxib (CE), an anti-inflammatory drug, potently enhances the therapeutic activity of AUR against colon cancer. Consequently, this study investigated the combined effects of AUR and CE on OS local progression and pulmonary metastases, in vivo.
C3H/HeSlc mice were implanted with the murine OS cell line, LM8. The mice were treated either with a vehicle control, AUR, or combination of AUR and CE (AUR-CE). The primary tumor size and weight were evaluated for the study duration and at resection, respectively. Hematoxylin and eosin and Ki-67 staining were performed to evaluate OS local progression and pulmonary metastases.
Mice in the AUR-CE group showed statistically significantly suppressed tumor sizes and weights at the time of excision compared with those in the vehicle. The mice in the AUR group did not show a statistically significant effect. Histopathological analysis of the primary tumor revealed a statistically significant decrease of the Ki-67-positive cells in the AUR-CE group compared with the vehicle group. Histopathological and quantitative analyses demonstrated that the AUR and AUR-CE groups had statistically significant reductions in the development of OS pulmonary metastases compared with the vehicle group.
The combination of AUR and CE significantly inhibited OS local progression and pulmonary metastases.
背景/目的:骨肉瘤(OS)是一种罕见的恶性肿瘤,存活率低。我们之前的研究报告称,硫氧还蛋白还原酶抑制剂金诺芬(AUR)可抑制 OS 肺转移;然而,OS 的局部进展不受影响。尽管如此,用 AUR 开发增强治疗以抑制 OS 局部进展仍然具有挑战性。塞来昔布(CE)是一种抗炎药,可强力增强 AUR 对结肠癌的治疗活性。因此,本研究探讨了 AUR 和 CE 联合对 OS 局部进展和肺转移的体内影响。
C3H/HeSlc 小鼠植入了小鼠骨肉瘤细胞系 LM8。小鼠分别用载体对照、AUR 或 AUR 和 CE 的组合(AUR-CE)治疗。在研究期间和切除时评估原发性肿瘤的大小和重量。进行苏木精和伊红以及 Ki-67 染色以评估 OS 局部进展和肺转移。
与载体组相比,AUR-CE 组的小鼠在切除时的肿瘤大小和重量均具有统计学显著抑制。AUR 组的小鼠没有表现出统计学显著的效果。对原发性肿瘤的组织病理学分析显示,AUR-CE 组的 Ki-67 阳性细胞明显少于载体组。组织病理学和定量分析表明,AUR 和 AUR-CE 组与载体组相比,OS 肺转移的发展明显减少。
AUR 和 CE 的联合显著抑制了 OS 的局部进展和肺转移。