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miR-29a-3p 通过抑制 CDC42BPA mRNA 表达抑制结直肠癌细胞系的迁移和侵袭。

Inhibition of cell migration and invasion by miR‑29a‑3p in a colorectal cancer cell line through suppression of CDC42BPA mRNA expression.

机构信息

Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia.

Department of Surgery, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia.

出版信息

Oncol Rep. 2017 Dec;38(6):3554-3566. doi: 10.3892/or.2017.6037. Epub 2017 Oct 16.

Abstract

The objective of this study was to determine the effect of miR‑29a‑3p inhibitor on the migration and invasion of colorectal cancer cell lines (CRC) and the underlying molecular mechanisms. miR‑29a‑3p was detected using reverse transcription-quantitative polymerase chain reaction (RT‑qPCR) in the CRC cell lines HCT11, CaCo2, HT29, SW480 and SW620. An invasive subpopulation designated SW480‑7 was derived from the parental cell line, detected by Transwell and Transwell Matrigel assays. Cytoskeleton Regulators RT2 profiler PCR array and western blot analysis were utilized to identify the alterations in expression of downstream mRNAs. siRNA against CDC42BPA was transfected into SW480‑7 and effects on cell migration and invasion were investigated. Data obtained showed that miR‑29a‑3p was detected in these five CRC cell lines. miR‑29a‑3p inhibitor had no effect on viability but stimulated cell migration and invasion of SW480‑7 cells. In contrast, miR‑29a‑3p mimic suppressed cell migration and invasion. TargetScan miRBD and DIANA were employed to identify the potential direct target genes of miR‑29a‑3p in the Cytoskeleton Regulators RT2-Profiler PCR array. Cytoskeleton Regulators RT2-Profiler PCR array data showed that 3 out of the 5 predicted targets genes, CDC42BPA (2.33-fold), BAIAP2 (1.79-fold) and TIAM1 (1.77-fold), in the array were upregulated by miR‑29a‑3p. A significant increase in expression IQGAP2, PHLDB2, SSH1 mRNAs and downregulation of PAK1 mRNA was also detected with miR‑29a‑3p inhibition. Increase in CDC42BPA, SSH1 and IQGAP2 mRNA expression correlated with increased protein level in miR‑29a‑3p transfected SW-480-7 cells. Silencing of CDC42BPA (an enhancer of cell motility) partially abolished miR‑29a‑3p inhibitor-induced stimulation of cell migration and invasion. miR‑29a‑3p expression in stage II and III CRC is relatively lower than that of stage I CRC. However, the data need to be interpreted with caution due to the small sample size. In conclusion, inhibition of miR‑29a‑3p stimulates SW480‑7 cell migration and invasion and downstream expression IQGAP2, PHLDB2, SSH1 mRNAs are upregulated whilst PAK1 mRNA is downregulated. Silencing of CDC42BPA expression partially reduces miR29a‑3p inhibitor-induced migration and invasion of SW480‑7 cells.

摘要

本研究旨在探讨 miR-29a-3p 抑制剂对结直肠癌细胞系(CRC)迁移和侵袭的影响及其潜在的分子机制。采用逆转录定量聚合酶链反应(RT-qPCR)检测 CRC 细胞系 HCT11、CaCo2、HT29、SW480 和 SW620 中 miR-29a-3p 的表达。通过 Transwell 和 Transwell Matrigel 测定,从亲本细胞系中分离出侵袭性亚群 SW480-7。细胞骨架调节剂 RT2 探针 PCR 阵列和 Western blot 分析用于鉴定下游 mRNA 表达的变化。将靶向 CDC42BPA 的 siRNA 转染至 SW480-7 细胞中,研究其对细胞迁移和侵袭的影响。结果显示,在这 5 种 CRC 细胞系中均检测到 miR-29a-3p。miR-29a-3p 抑制剂对 SW480-7 细胞的活力没有影响,但能刺激细胞迁移和侵袭。相反,miR-29a-3p 模拟物抑制细胞迁移和侵袭。采用 TargetScan miRBD 和 DIANA 对 Cytoskeleton Regulators RT2-Profiler PCR 阵列中的 miR-29a-3p 的潜在直接靶基因进行鉴定。Cytoskeleton Regulators RT2-Profiler PCR 阵列数据显示,在预测的 5 个靶基因中,有 3 个(CDC42BPA 为 2.33 倍,BAIAP2 为 1.79 倍,TIAM1 为 1.77 倍)的基因在 miR-29a-3p 作用下表达上调。还检测到 IQGAP2、PHLDB2 和 SSH1 mRNA 的表达显著增加,PAK1 mRNA 的表达下调。miR-29a-3p 抑制作用还导致 PHLDB2、SSH1 和 IQGAP2 mRNA 的表达增加,与转染 miR-29a-3p 的 SW-480-7 细胞中蛋白水平的增加相关。CDC42BPA(一种增强细胞运动的因子)的沉默部分消除了 miR-29a-3p 抑制剂诱导的细胞迁移和侵袭的刺激作用。在 II 期和 III 期 CRC 中 miR-29a-3p 的表达水平相对低于 I 期 CRC,但由于样本量较小,数据需谨慎解释。综上所述,miR-29a-3p 的抑制作用可刺激 SW480-7 细胞的迁移和侵袭,下游表达的 IQGAP2、PHLDB2、SSH1 mRNA 上调,而 PAK1 mRNA 下调。CDC42BPA 表达的沉默部分减少了 miR29a-3p 抑制剂诱导的 SW480-7 细胞的迁移和侵袭。

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