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HIF-1α 通过调节 miR-210 促进乳腺癌 MCF-7 细胞的增殖和侵袭。

HIF-1α Promotes Breast Cancer Cell MCF-7 Proliferation and Invasion Through Regulating miR-210.

机构信息

Department of Surgical Oncology, Tangshan People's Hospital , Tangshan, China .

出版信息

Cancer Biother Radiopharm. 2017 Oct;32(8):297-301. doi: 10.1089/cbr.2017.2270.

Abstract

OBJECTIVE

Many malignant tumors grow in hypoxic condition, which is associated with tumor growth, invasion, and metastasis. MicroRNAs are of great significance in the development of multiple malignant tumors. This study cultured breast cancer cell MCF-7 under the condition of different concentrations of oxygen, to test cell proliferation and invasion, and detect miR-210 expression, aiming to analyze the influence of hypoxia on breast cancer cell behaviors as well as miR-210 expressions.

MATERIALS AND METHODS

Breast cancer cell MCF-7 was cultured under normoxia, hypoxia, or anaerobic conditions for 12, 24, or 48 hours. Cell proliferation was detected by MTT assay. Cell invasion and migration were tested by transwell assay. HIF-1α mRNA and miR-210 expressions were determined by real-time polymerase chain reaction.

RESULTS

MCF-7 cell proliferation was gradually increased following time extension (p < 0.05). MCF-7 cell exhibited higher proliferation, invasion, and migration activities in hypoxic and anaerobic groups compared with those in normoxic group during the same time period. HIF-1α mRNA and miR-210 were significantly upregulated in anaerobic group compared with those in other groups (p < 0.05). HIF-1α mRNA and miR-210 were obviously elevated at 12, 24, and 48 hours (p < 0.05).

CONCLUSION

MCF-7 cell proliferation was increased, invasion and migration were enhanced, with upregulated expression of HIF-1α mRNA and miR-210 in the hypoxic and anaerobic group following time extension.

摘要

目的

许多恶性肿瘤在缺氧条件下生长,这与肿瘤的生长、侵袭和转移有关。microRNAs 在多种恶性肿瘤的发生发展中具有重要意义。本研究在不同氧浓度条件下培养乳腺癌细胞 MCF-7,检测细胞增殖和侵袭,检测 miR-210 的表达,旨在分析缺氧对乳腺癌细胞行为以及 miR-210 表达的影响。

材料和方法

乳腺癌细胞 MCF-7 在常氧、缺氧或厌氧条件下培养 12、24 或 48 小时。MTT 法检测细胞增殖。Transwell 法检测细胞侵袭和迁移。实时聚合酶链反应检测 HIF-1α mRNA 和 miR-210 的表达。

结果

随着时间的延长,MCF-7 细胞的增殖逐渐增加(p<0.05)。与常氧组相比,在同一时间内,缺氧和厌氧组的 MCF-7 细胞增殖、侵袭和迁移活性更高。与其他组相比,厌氧组的 HIF-1α mRNA 和 miR-210 明显上调(p<0.05)。HIF-1α mRNA 和 miR-210 在 12、24 和 48 小时明显升高(p<0.05)。

结论

随着时间的延长,MCF-7 细胞增殖增加,侵袭和迁移增强,HIF-1α mRNA 和 miR-210 的表达上调。

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