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miRNA-621 通过靶向 SIX4 抑制非小细胞肺癌的恶性进展。

MiRNA-621 inhibits the malignant progression of non-small cell lung cancer via targeting SIX4.

机构信息

Department of Thoracic Surgery, Shengzhou Renmin Hospital, Shengzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Jun;23(11):4807-4814. doi: 10.26355/eurrev_201906_18066.

Abstract

OBJECTIVE

To clarify the role of microRNA-621 (miRNA-621)/SIX4 axis in regulating the malignant progression of non-small cell lung cancer (NSCLC) and the potential mechanism.

PATIENTS AND METHODS

MiRNA-621 expression in NSCLC tissues and paracancerous tissues (n=50) was examined by quantitative Real-time polymerase chain reaction (qRT-PCR). We further analyzed the correlation between miRNA-621 expression and pathological indexes of NSCLC patients. By transfection of miRNA-621 mimics, its expression was upregulated. Regulatory effects of miRNA-621 on proliferation and apoptosis of H1299 and SPC-A1 cells were evaluated by cell counting kit-8 (CCK-8), 5-Ethynyl-2'- deoxyuridine (EdU) assay and flow cytometry, respectively. Finally, the potential mechanism of miRNA-621 in regulating target gene SIX4 was explored by Western blot and rescue experiments.

RESULTS

MiRNA-621 was lowly expressed in NSCLC tissues relative to paracancerous tissues. NSCLC patients with low-level miRNA-621 were expected to have a worse clinical grade and shorter overall survival compared with those with a high level. Transfection of miRNA-621 mimics in H1299 and SPC-A1 cells markedly suppressed proliferation, but induced apoptosis. SIX4 was found to be highly expressed in NSCLC and negatively regulated by miRNA-621. MiRNA-621 overexpression could downregulate protein levels of SIX4, CD31, Ki-67, c-Myc, MMP-2 and MMP-9 in H1299 and SPC-A1 cells. Overexpression of SIX4 partially reversed the role of miRNA-621 in the malignant progression of NSCLC.

CONCLUSIONS

MiRNA-621 is closely related to pathological grade and poor prognosis of NSCLC. Besides, miRNA-621 can inhibit the malignant progression of NSCLC by regulating SIX4 expression.

摘要

目的

阐明微小 RNA-621(miRNA-621)/SIX4 轴在调控非小细胞肺癌(NSCLC)恶性进展中的作用及潜在机制。

患者与方法

采用实时定量聚合酶链反应(qRT-PCR)检测 NSCLC 组织及癌旁组织中 miRNA-621 的表达情况,进一步分析 miRNA-621 表达与 NSCLC 患者病理指标的相关性。通过转染 miRNA-621 模拟物上调其表达,采用细胞计数试剂盒-8(CCK-8)、5-乙炔基-2'-脱氧尿苷(EdU)实验和流式细胞术分别评估 miRNA-621 对 H1299 和 SPC-A1 细胞增殖和凋亡的调控作用,最后通过 Western blot 和挽救实验探讨 miRNA-621 调控靶基因 SIX4 的潜在机制。

结果

miRNA-621 在 NSCLC 组织中相对低表达,且 NSCLC 患者中低水平 miRNA-621 与较差的临床分级和较短的总生存期相关。转染 miRNA-621 模拟物可显著抑制 H1299 和 SPC-A1 细胞的增殖,但诱导细胞凋亡。SIX4 在 NSCLC 中高表达,并受 miRNA-621 的负调控。miRNA-621 过表达可下调 H1299 和 SPC-A1 细胞中 SIX4、CD31、Ki-67、c-Myc、MMP-2 和 MMP-9 的蛋白水平。过表达 SIX4 可部分逆转 miRNA-621 在 NSCLC 恶性进展中的作用。

结论

miRNA-621 与 NSCLC 的病理分级和不良预后密切相关,此外,miRNA-621 可通过调节 SIX4 表达抑制 NSCLC 的恶性进展。

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