Department of Cancer Biology, The University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Division of Hematology and Oncology, Children's Mercy Hospital, Kansas City, MO, 64108, USA.
Cell Death Dis. 2020 Feb 24;11(2):149. doi: 10.1038/s41419-020-2335-1.
Osteosarcoma (OS) is the most common primary bone tumor that primarily affects children and adolescents. Studies suggested that dysregulation JAK/STAT signaling promotes the development of OS. Cells treated with pimozide, a STAT5 inhibitor suppressed proliferation and colony formation and induced sub G0/G1 cell cycle arrest and apoptosis. There was a reduction in cyclin D1 and CDK2 expression and Rb phosphorylation, and activation of Caspase-3 and PARP cleavage. In addition, pimozide suppressed the formation of 3-dimensional osteospheres and growth of the cells in the Tumor in a Dish lung organoid system. Furthermore, there was a reduction in expression of cancer stem cell marker proteins DCLK1, CD44, CD133, Oct-4, and ABCG2. More importantly, it was the short form of DCLK1 that was upregulated in osteospheres, which was suppressed in response to pimozide. We further confirmed by flow cytometry a reduction in DCLK1+ cells. Moreover, pimozide inhibits the phosphorylation of STAT5, STAT3, and ERK in OS cells. Molecular docking studies suggest that pimozide interacts with STAT5A and STAT5B with binding energies of -8.4 and -6.4 Kcal/mol, respectively. Binding was confirmed by cellular thermal shift assay. To further understand the role of STAT5, we knocked down the two isoforms using specific siRNAs. While knockdown of the proteins did not affect the cells, knockdown of STAT5B reduced pimozide-induced necrosis and further enhanced late apoptosis. To determine the effect of pimozide on tumor growth in vivo, we administered pimozide intraperitoneally at a dose of 10 mg/kg BW every day for 21 days in mice carrying KHOS/NP tumor xenografts. Pimozide treatment significantly suppressed xenograft growth. Western blot and immunohistochemistry analyses also demonstrated significant inhibition of stem cell marker proteins. Together, these data suggest that pimozide treatment suppresses OS growth by targeting both proliferating cells and stem cells at least in part by inhibiting the STAT5 signaling pathway.
骨肉瘤(OS)是一种主要影响儿童和青少年的最常见原发性骨肿瘤。研究表明,JAK/STAT 信号通路的失调促进了 OS 的发展。用匹莫齐特(一种 STAT5 抑制剂)处理的细胞抑制了增殖和集落形成,并诱导了亚 G0/G1 细胞周期停滞和细胞凋亡。细胞周期蛋白 D1 和 CDK2 的表达以及 Rb 磷酸化减少,Caspase-3 和 PARP 切割被激活。此外,匹莫齐特抑制了三维成骨球体的形成和 Tumor in a Dish 肺类器官系统中细胞的生长。此外,癌症干细胞标记蛋白 DCLK1、CD44、CD133、Oct-4 和 ABCG2 的表达减少。更重要的是,在成骨球体中上调的是 DCLK1 的短形式,而该形式在匹莫齐特的作用下被抑制。我们通过流式细胞术进一步证实了 DCLK1+细胞的减少。此外,匹莫齐特抑制 OS 细胞中 STAT5、STAT3 和 ERK 的磷酸化。分子对接研究表明,匹莫齐特与 STAT5A 和 STAT5B 相互作用,结合能分别为-8.4 和-6.4 Kcal/mol。通过细胞热转移试验证实了结合。为了进一步了解 STAT5 的作用,我们使用特异性 siRNA 敲低了两种同工型。虽然蛋白的敲低不影响细胞,但 STAT5B 的敲低减少了匹莫齐特诱导的坏死,并进一步增强了晚期凋亡。为了确定匹莫齐特在体内对肿瘤生长的影响,我们在携带 KHOS/NP 肿瘤异种移植物的小鼠中每天腹膜内给予 10 mg/kg BW 的匹莫齐特 21 天。匹莫齐特治疗显著抑制了异种移植物的生长。Western blot 和免疫组化分析也表明干细胞标记蛋白的显著抑制。综上所述,这些数据表明,匹莫齐特通过至少部分抑制 STAT5 信号通路,抑制增殖细胞和干细胞,从而抑制 OS 的生长。