Veys Clément, Boulouard Flavie, Benmoussa Abderrahim, Jammes Manon, Brotin Emilie, Rédini Françoise, Poulain Laurent, Gruchy Nicolas, Denoyelle Christophe, Legendre Florence, Galera Philippe
Normandie Univ., UNICAEN, BIOTARGEN, Caen, France.
Department of Genetics, Normandy Center for Genomic and Personalized Medicine, Caen University Hospital, Caen, France.
Front Oncol. 2023 Aug 31;13:1220459. doi: 10.3389/fonc.2023.1220459. eCollection 2023.
Chondrosarcomas and osteosarcomas are malignant bone tumors with a poor prognosis when unresectable or metastasized. Moreover, radiotherapy and chemotherapy could be ineffective. MiRNAs represent an alternative therapeutic approach. Based on high-throughput functional screening, we identified four miRNAs with a potential antiproliferative effect on SW1353 chondrosarcoma cells. Individual functional validations were then performed in SW1353 cells, as well as in three osteosarcoma cell lines. The antiproliferative and cytotoxic effects of miRNAs were evaluated in comparison with a positive control, miR-342-5p. The cytotoxic effect of four selected miRNAs was not confirmed on SW1353 cells, but we unambiguously revealed that miR-4270 had a potent cytotoxic effect on HOS and MG-63 osteosarcoma cell lines, but not on SaOS-2 cell line. Furthermore, like miR-342-5p, miR-4270 induced apoptosis in these two cell lines. In addition, we provided the first report of Bcl-xL as a direct target of miR-4270. MiR-4270 also decreased the expression of the anti-apoptotic protein Mcl-1, and increased the expression of the pro-apoptotic protein Bak. Our findings demonstrated that miR-4270 has tumor suppressive activity in osteosarcoma cells, particularly through Bcl-xL downregulation.
软骨肉瘤和骨肉瘤是恶性骨肿瘤,当无法切除或发生转移时预后较差。此外,放疗和化疗可能无效。微小RNA(miRNA)代表了一种替代治疗方法。基于高通量功能筛选,我们鉴定出四种对SW1353软骨肉瘤细胞具有潜在抗增殖作用的miRNA。然后在SW1353细胞以及三种骨肉瘤细胞系中进行了个体功能验证。与阳性对照miR-342-5p相比,评估了miRNA的抗增殖和细胞毒性作用。在SW1353细胞上未证实四种选定miRNA的细胞毒性作用,但我们明确发现miR-4270对HOS和MG-63骨肉瘤细胞系具有强大的细胞毒性作用,但对SaOS-2细胞系没有作用。此外,与miR-342-5p一样,miR-4270在这两种细胞系中诱导细胞凋亡。此外,我们首次报道了Bcl-xL是miR-4270的直接靶点。miR-4270还降低了抗凋亡蛋白Mcl-1的表达,并增加了促凋亡蛋白Bak的表达。我们的研究结果表明,miR-4270在骨肉瘤细胞中具有肿瘤抑制活性,特别是通过下调Bcl-xL实现的。