Department of Orthopedic Disease and Oncology Surgery, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Department of Orthopedics, Fourth Affiliated Hospital of Anhui Medical University, Hefei, China.
Bosn J Basic Med Sci. 2021 Apr 1;21(2):163-173. doi: 10.17305/bjbms.2020.4485.
The transforming growth factor alpha (TGFA) gene is involved in the proliferation and metastasis of various tumors, but its role in cell sensitivity to cisplatin chemotherapy is unclear. In this study, we investigated the mechanism underlying inhibitory effects of cisplatin on growth and proliferation of osteosarcoma cells. Osteosarcoma and normal skeletal muscle tissues were collected from 26 patients by biopsy. TGFA was silenced or overexpressed in Saos-2 osteosarcoma cells by transfection with TGFA-shRNA or TGFA ORF clone, respectively. MiR-376c was inhibited or overexpressed by transfection of Saos-2 cells with miR-376c sponge or miR-376c mimics, respectively. Cell growth was analyzed by MTT assay and cell proliferation by BrdU assay. MiR-376c and TGFA mRNA expression was detected by quantitative reverse transcription PCR and TGFA protein expression by Western blot. The target relationship between miR-376c and TGFA was assessed by luciferase reporter assay. Both in osteosarcoma tissues and Saos-2 cells, miR-376c expression was significantly decreased and TGFA mRNA expression was significantly increased compared with control. Transfection of Saos-2 cells with TGFA-shRNA silenced TGFA expression and significantly inhibited cell growth and proliferation. TGFA mRNA and protein expression in Saos-2 cells significantly decreased with increasing cisplatin concentrations (2.5-10 mg/L). Transfection with TGFA ORF clone reversed the inhibitory effects of cisplatin on Saos-2 cell proliferation. Compared with cisplatin (10 mg/L) treatment alone, the combined treatment with cisplatin and miR-376c mimics inhibited the proliferation of Saos-2 cells more significantly. MiR-376c suppressed TGFA expression by directly interacting with its 3' UTR region. Overall, cisplatin inhibited the proliferation of Saos-2 cells by upregulating miR-376c and downregulating TGFA expression.
转化生长因子α(TGFA)基因参与多种肿瘤的增殖和转移,但它在细胞对顺铂化疗敏感性中的作用尚不清楚。在本研究中,我们研究了顺铂抑制骨肉瘤细胞生长和增殖的机制。通过活检从 26 名患者中收集骨肉瘤和正常骨骼肌组织。分别通过 TGFA-shRNA 或 TGFA ORF 克隆转染沉默或过表达 Saos-2 骨肉瘤细胞中的 TGFA。分别通过转染 Saos-2 细胞 miR-376c 海绵或 miR-376c 模拟物抑制或过表达 miR-376c。通过 MTT 分析检测细胞生长,通过 BrdU 分析检测细胞增殖。通过定量逆转录 PCR 检测 miR-376c 和 TGFA mRNA 表达,通过 Western blot 检测 TGFA 蛋白表达。通过荧光素酶报告测定评估 miR-376c 和 TGFA 之间的靶关系。与对照组相比,骨肉瘤组织和 Saos-2 细胞中的 miR-376c 表达明显降低,TGFA mRNA 表达明显升高。转染 Saos-2 细胞的 TGFA-shRNA 沉默 TGFA 表达并显著抑制细胞生长和增殖。随着顺铂浓度(2.5-10 mg/L)的增加,Saos-2 细胞中 TGFA mRNA 和蛋白表达显著降低。转染 TGFA ORF 克隆逆转了顺铂对 Saos-2 细胞增殖的抑制作用。与单独顺铂(10 mg/L)处理相比,顺铂和 miR-376c 模拟物联合处理更显著地抑制了 Saos-2 细胞的增殖。miR-376c 通过直接与其 3'UTR 区域相互作用抑制 TGFA 表达。总的来说,顺铂通过上调 miR-376c 和下调 TGFA 表达抑制 Saos-2 细胞的增殖。