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miR-29 和 STAT3 在骨肉瘤中的表达及其对骨肉瘤细胞增殖调控的影响。

Expression of miR-29 and STAT3 in osteosarcoma and its effect on proliferation regulation of osteosarcoma cells.

机构信息

Department of Orthopedics, the Fifth Hospital of Wuhan, Wuhan, Hubei, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Sep;23(17):7275-7282. doi: 10.26355/eurrev_201909_18832.

Abstract

OBJECTIVE

STAT3 has been shown to be involved in the occurrence, progression, and resistance of various tumors. The abnormal expression of miR-29 is associated with the pathogenesis of osteosarcoma. The bioinformatics analysis showed a targeting relationship between miR-29 and STAT3 3'-UTR. This study investigated whether miR-29 regulates the STAT3 expression and affects the proliferation and apoptosis of osteosarcoma cells.

PATIENTS AND METHODS

The tumor tissues of osteosarcoma patients were collected, and the adjacent tissues were used as controls to detect the expression of miR-29 and STAT3. The Dual-Luciferase Gene Reporter Assay validated the regulatory relationship between miR-29 and STAT3. The expression of miR-29 and STAT3 in normal osteoblasts hFOB1.19, osteosarcoma SJSA-1, and MG-63 was measured. SJSA-1 cells were divided into miR-NC group and miR-29 mimic group. Cell apoptosis and proliferation were detected by flow cytometry.

RESULTS

Compared with adjacent tissues, miR-29 expression was decreased, and STAT3 expression was increased in osteosarcoma. There was a targeted regulation relationship between miR-29 and STAT3. Compared with hFOB1.19 cells, miR-29 expression in osteosarcoma SJSA-1 and MG-63 cells was decreased, with increased STAT3 expression. The transfection of miR-29 mimic significantly decreased the expression of STAT3 and p-STAT3 in SJSA-1 cells, inhibited cell proliferation, and increased cell apoptosis.

CONCLUSIONS

Decreased miR-29 expression plays a role in the increase of the STAT3 expression and in the promotion of the pathogenesis of osteosarcoma. Increasing the expression of miR-29 can inhibit the proliferation of osteosarcoma cells and promote apoptosis by decreasing STAT3 expression.

摘要

目的

STAT3 已被证明参与多种肿瘤的发生、进展和耐药。miR-29 的异常表达与骨肉瘤的发病机制有关。生物信息学分析显示 miR-29 与 STAT3 3'-UTR 之间存在靶向关系。本研究探讨了 miR-29 是否调节 STAT3 表达并影响骨肉瘤细胞的增殖和凋亡。

患者和方法

收集骨肉瘤患者的肿瘤组织,以相邻组织作为对照,检测 miR-29 和 STAT3 的表达。双荧光素酶基因报告实验验证了 miR-29 和 STAT3 之间的调控关系。检测正常成骨细胞 hFOB1.19、骨肉瘤 SJSA-1 和 MG-63 中 miR-29 和 STAT3 的表达。将 SJSA-1 细胞分为 miR-NC 组和 miR-29 模拟物组。通过流式细胞术检测细胞凋亡和增殖。

结果

与相邻组织相比,骨肉瘤中 miR-29 表达降低,STAT3 表达升高。miR-29 与 STAT3 之间存在靶向调控关系。与 hFOB1.19 细胞相比,骨肉瘤 SJSA-1 和 MG-63 细胞中 miR-29 表达降低,STAT3 表达升高。miR-29 模拟物转染后,SJSA-1 细胞中 STAT3 和 p-STAT3 的表达明显降低,细胞增殖受到抑制,细胞凋亡增加。

结论

miR-29 表达降低在 STAT3 表达增加和促进骨肉瘤发病机制中起作用。增加 miR-29 的表达可以通过降低 STAT3 表达抑制骨肉瘤细胞的增殖并促进凋亡。

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