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长链非编码 RNA(lncRNA)小核仁 RNA 宿主基因 7(SNHG7)通过海绵吸附 miRNA-381 促进乳腺癌的进展。

Long non-coding RNA (lncRNA) small nucleolar RNA host gene 7 (SNHG7) promotes breast cancer progression by sponging miRNA-381.

机构信息

College of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Aug;23(15):6588-6595. doi: 10.26355/eurrev_201908_18545.

Abstract

OBJECTIVE

The abnormal expression of lncRNA small nucleolar RNA host gene 7 (SNHG7) has been found in various kinds of cancers but its expression and role in breast cancer are unknown. We conducted this study to identify the expression, the function, and to underline the mechanism of SNHG7 in breast cancer.

PATIENTS AND METHODS

The expression of SNHG7 was evaluated in clinical breast cancer tissues and adjacent normal tissues by qPCR assays. The expression was also detected in breast cancer cell lines and normal cell line. CCK8 assays were used to determine the biological functions of SNHG7 on breast cancer cells' proliferation. The transwell assays were applied for the exploration of the effects of SNHG7 on breast cancer cells' invasion. The direct target of SNHG7 was predicted by bioinformatics algorithm and verified by the Luciferase reporter assays.

RESULTS

SNHG7 was found to be significantly upregulated in breast cancer tissues when compared with normal tissues. Breast cancer cell lines showed higher levels of SNHG7 than normal breast epithelial cell line. The knockdown of SNHG7 by siRNA could remarkably repress breast cancer cell proliferation and invasion. Moreover, miRNA-381 was newly confirmed as a direct target of SNHG7 and it mediated the suppressing effects of SNHG7 on breast cancer cells.

CONCLUSIONS

SNHG7 was significantly upregulated in breast cancer and acted as an oncogene to promote breast cancer cell proliferation and invasion by directly sponging miRNA-381.

摘要

目的

长链非编码 RNA 小核仁 RNA 宿主基因 7(SNHG7)的异常表达已在多种癌症中被发现,但它在乳腺癌中的表达和作用尚不清楚。我们进行这项研究旨在确定 SNHG7 在乳腺癌中的表达、功能和作用机制。

患者和方法

通过 qPCR 检测临床乳腺癌组织和相邻正常组织中 SNHG7 的表达。还检测了乳腺癌细胞系和正常细胞系中的表达。CCK8 测定用于确定 SNHG7 对乳腺癌细胞增殖的生物学功能。Transwell 测定用于研究 SNHG7 对乳腺癌细胞侵袭的影响。通过生物信息学算法预测 SNHG7 的直接靶标,并通过荧光素酶报告测定验证。

结果

与正常组织相比,SNHG7 在乳腺癌组织中明显上调。乳腺癌细胞系中的 SNHG7 水平高于正常乳腺上皮细胞系。通过 siRNA 敲低 SNHG7 可显著抑制乳腺癌细胞的增殖和侵袭。此外,miRNA-381 被新确认为 SNHG7 的直接靶标,它介导了 SNHG7 对乳腺癌细胞的抑制作用。

结论

SNHG7 在乳腺癌中明显上调,通过直接海绵吸附 miRNA-381,作为癌基因促进乳腺癌细胞增殖和侵袭。

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