Department of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Department of Hepatobiliary Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
J Cell Physiol. 2020 Jul;235(7-8):5711-5721. doi: 10.1002/jcp.29506. Epub 2020 Jan 23.
Dysregulation of microRNAs (miRNAs) expression has been demonstrated in gastrointestinal stromal tumor (GIST). In this study, we aimed to determine the differential miRNAs expression in GISTs and explore the functional mechanism of differential miRNAs in GIST cells. We measured differential miRNAs in six pairs of GIST tissues and matched adjacent tissues through a high-throughput sequencing, which was confirmed in 64 pairs of GIST tissues and adjacent tissues by real-time polymerase chain reaction. We found that miR-4510 expression was significantly downregulated in GIST tissues compared to matched control tissues. Luciferase reporter assay identified apolipoprotein C-II (APOC2) as a direct target of miR-4510. Overexpression of miR-4510 inhibited the mRNA and protein expression of APOC2. In addition, overexpression of miR-4510 suppressed GIST cell proliferation, migration, and invasion. Overexpression of miR-4510 also inhibited the phosphorylation of AKT and ERK1/2, reduced the expression of matrix metallopeptidase 2 (MMP2) and MMP9. APOC2 knockdown mimicked the effect of miR-4510 overexpression. Further investigation confirmed that APOC2 was notably upregulated in GIST tissues compared to adjacent control tissues. These results suggested that miR-4510 downregulation could promote GIST progression, including growth, invasion, and metastasis, through increasing APOC2 expression.
miRNAs 表达失调已在胃肠道间质瘤(GIST)中得到证实。在这项研究中,我们旨在确定 GIST 中差异 miRNAs 的表达,并探索差异 miRNAs 在 GIST 细胞中的功能机制。我们通过高通量测序测量了六对 GIST 组织和配对的相邻组织中的差异 miRNAs,并用实时聚合酶链反应在 64 对 GIST 组织和相邻组织中进行了验证。我们发现 miR-4510 的表达在 GIST 组织中与匹配的对照组织相比明显下调。荧光素酶报告基因检测鉴定载脂蛋白 C-II(APOC2)为 miR-4510 的直接靶标。miR-4510 的过表达抑制了 APOC2 的 mRNA 和蛋白表达。此外,miR-4510 的过表达抑制了 GIST 细胞的增殖、迁移和侵袭。miR-4510 的过表达还抑制了 AKT 和 ERK1/2 的磷酸化,降低了基质金属蛋白酶 2(MMP2)和 MMP9 的表达。APOC2 的敲低模拟了 miR-4510 过表达的效果。进一步的研究证实,APOC2 在 GIST 组织中的表达明显高于相邻对照组织。这些结果表明,miR-4510 的下调可能通过增加 APOC2 的表达促进 GIST 的进展,包括生长、侵袭和转移。