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LncRNA ZFAS1/miR-589 regulates the PTEN/PI3K/AKT signal pathway in the proliferation, invasion and migration of breast cancer cells

机译:LncRNA ZFAS1/miR-589 调控乳腺癌细胞增殖、侵袭和迁移中的 PTEN/PI3K/AKT 信号通路

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摘要

Breast cancer (BC) is a common clinical disease and the second leading cause of cancer death in women. Long noncoding RNA (lncRNA) and microRNA (miRNA) are reported to be involved in the development of BC. The present study aimed to investigate whether LncRNA ZFAS1 could regulate the proliferation, invasion and migration of breast cancer cells by targeting miR-589 through PTEN/PI3K/AKT signal pathway. The expression of ZFAS1 and miR-589 in BC cells and transfection effects were determined by RT-qPCR analysis. The abilities of proliferation, colony formation, invasion and migration of breast cancer cells were analyzed by CCK-8 assay, colony formation assay, transwell assay and wound healing assay respectively. The expression of MMP2, MMP9, Bcl2, Bax, cleaved caspase3, PTEN, p-PI3K, p-AKT, PI3K and AKT was detected by Western blot. The flow cytometry analysis was used to detect cell apoptosis. As a result, ZFAS1 expression was increased and miR-589 expression was decreased in BC cells. And, miR-589 was demonstrated to be a target of ZFAS1. ZFAS1 overexpression could inhibit the proliferation, colony formation, invasion and migration of BC cells while miR-589 overexpression could reverse the changes. In addition, ZFAS1 overexpression suppressed the expression of PI3K/AKT signal pathway by activating the PTEN expression while miR-589 overexpression could reverse the changes. Moreover, PTEN is one of the gene targets of miR-589. In conclusion, this study indicated that ZFAS1 inhibited the proliferation, invasion and migration of breast cancer cells by targeting miR-589 through regulating the PTEN/PI3K/AKT signal pathway.
机译:乳腺癌 (BC) 是一种常见的临床疾病,也是女性癌症死亡的第二大原因。据报道,长链非编码 RNA (lncRNA) 和 microRNA (miRNA) 参与 BC 的发育。本研究旨在探讨LncRNA ZFAS1是否通过PTEN/PI3K/AKT信号通路靶向miR-589来调节乳腺癌细胞的增殖、侵袭和迁移。通过RT-qPCR分析测定ZFAS1和miR-589在BC细胞中的表达和转染效应。采用CCK-8法、集落形成法、transwell法和伤口愈合法分别分析乳腺癌细胞的增殖、集落形成、侵袭和迁移能力。Western blot检测MMP2、MMP9、Bcl2、Bax、裂解半胱天冬酶3、PTEN、p-PI3K、p-AKT、PI3K和AKT的表达。流式细胞术分析检测细胞凋亡。结果,BC细胞中ZFAS1表达增加,miR-589表达降低。而且,miR-589 被证明是 ZFAS1 的靶标。ZFAS1过表达可抑制BC细胞的增殖、集落形成、侵袭和迁移,而miR-589过表达可逆转其变化。此外,ZFAS1过表达通过激活PTEN表达抑制PI3K/AKT信号通路的表达,而miR-589过表达可以逆转其变化。此外,PTEN是miR-589的基因靶标之一。综上所述,ZFAS1通过调节PTEN/PI3K/AKT信号通路靶向miR-589,抑制乳腺癌细胞的增殖、侵袭和迁移。

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