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微小 RNA-791 是甲状腺乳头状癌的独立预后因素,可抑制 PTC 细胞的增殖。

MicroRNA-791 is an independent prognostic factor of papillary thyroid carcinoma and inhibits the proliferation of PTC cells.

机构信息

Department of Surgery for Vascular Thyroid and Hernia, Xuzhou Central Hospital, Xuzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Sep;22(17):5562-5568. doi: 10.26355/eurrev_201809_15819.

Abstract

OBJECTIVE

To investigate the significance and possible mechanism of miR-791 in the pathogenesis of papillary thyroid carcinoma (PTC).

PATIENTS AND METHODS

The expression of miR-791 in 80 cases of thyroid carcinoma tissues and 80 cases of paracancerous tissues was detected by quantitative Real-time-polymerase chain reaction (qRT-PCR). After miR-791 mimics were transfected into thyroid cancer cells by liposome method, the cell proliferation was detected by Cell Counting Kit-8 (CCK-8) and 5-ethynyl-2'-deoxyuridine (EDU), respectively. Cell cycle was detected by flow cytometry.

RESULTS

The expression of miR-791 in thyroid cancer tissue was significantly lower than that of normal thyroid. The mir-719 expression is positively correlated with the prognosis of thyroid carcinoma. After transfection of miR-791 mimics, the proliferation ability of TPC-1 and HTH83 cells was weakened, and the cell cycle was blocked in the G0/G1 phase. Further study on the underlying mechanism found that after overexpression of miR-791, the expressions of Cyclin D1, CKD6 and CDK4 decreased significantly, while the expression of cyclin inhibitor P21 increased significantly.

CONCLUSIONS

MiR-791 is lowly expressed in thyroid cancer. MiR-791 may inhibit thyroid cancer cell proliferation by blocking thyroid cancer cells in G0/G1 phase, thus participating in the impediment of thyroid cancer development.

摘要

目的

探讨 miR-791 在甲状腺癌(PTC)发病机制中的意义和可能机制。

患者和方法

采用实时荧光定量聚合酶链反应(qRT-PCR)检测 80 例甲状腺癌组织和 80 例癌旁组织中 miR-791 的表达。采用脂质体法将 miR-791 模拟物转染入甲状腺癌细胞后,分别用细胞计数试剂盒(CCK-8)和 5-乙炔基-2'-脱氧尿苷(EDU)检测细胞增殖。用流式细胞术检测细胞周期。

结果

甲状腺癌组织中 miR-791 的表达明显低于正常甲状腺。mir-719 的表达与甲状腺癌的预后呈正相关。转染 miR-791 模拟物后,TPC-1 和 HTH83 细胞的增殖能力减弱,细胞周期被阻滞在 G0/G1 期。进一步的机制研究发现,过表达 miR-791 后,Cyclin D1、CKD6 和 CDK4 的表达明显下降,而细胞周期蛋白抑制剂 P21 的表达明显增加。

结论

miR-791 在甲状腺癌中低表达。miR-791 可能通过阻滞甲状腺癌细胞在 G0/G1 期来抑制甲状腺癌细胞增殖,从而参与甲状腺癌的发生发展。

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