含66的CircRNA coil - coil结构域上调lim同源结构域基因2通过Sponing miR-129-5p促进胃癌进展

IF 2.9 4区 医学 Q1 Medicine Journal of biomedical nanotechnology Pub Date : 2023-09-01 DOI:10.1166/jbn.2023.3662
Mingzhi Cai, Qiuxian Chen, Lisheng Cai, Yuqin Sun, Wenshan Zhang
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引用次数: 0

摘要

胃癌的死亡率不断上升,但早期诊断和治疗方法仍然有限。CircRNAs能够与miRNA结合,对多种癌症发挥治疗作用。本研究旨在探讨circ-CCDC66在GC中的作用机制。采用qRT-PCR和Western blot检测CCDC66、miR-129-5p、LHX2 mRNA及蛋白的表达。流式细胞术和Western blot检测细胞凋亡。采用双荧光素酶报告基因法验证miR-129-5p与CCDC66或LHX2的结合位点。采用Transwell法和细胞计数试剂盒8 (CCK-8)检测细胞增殖能力、迁移或侵袭能力。与正常组织相比,GC组织中CCDC66表达明显升高,miR-129-5p表达明显降低。敲低circ-CCDC66可改变胃癌细胞的恶性行为。MiR-129-5p抑制剂改变下调的circ-CCDC66对胃癌细胞恶性行为的影响。LHX2与miR-129-5p结合,circ-CCDC66调节LHX2表达,通过miR-129-5p参与GC进展。以上结果提示,CCDC66可通过抑制miR-129-5p调节LHX2表达,促进胃癌进展,可能为胃癌治疗提供关键策略。
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CircRNA Coiled-Coil Domain Containing 66 Up-Regulates LIM-Homeodomain Gene 2 to Promote Gastric Cancer Progression via Sponing miR-129-5p
The death rate from gastric cancer (GC) is increasing while the methods of early diagnosis and treatment of GC are still limited. CircRNAs have ability to bind with miRNA to exert therapeutic action on kinds of cancers. The purpose of this study was to explore the action mechanism of circ-CCDC66 in GC. CCDC66, miR-129-5p and LHX2 mRNA and protein expression were examine by qRT-PCR and Western blot. Flow cytometry and Western blot were used to identify cells apoptosis. Dual-luciferase reporter assay was applied to verified the binding site that miR-129-5p and CCDC66 or LHX2. Transwell assay and cell account kit 8 (CCK-8) were used to examined cells proliferation ability, migration or invasion ability. Compared with normal tissues, CCDC66 expression was obviously higher and miR-129-5p expression was significantly lower in GC tissues. Knockdown circ-CCDC66 changed malignant behavior of GC cells. MiR-129-5p inhibitor changed the effect of down-regulated circ-CCDC66 on malignant behavior of gastric cancer cells. LHX2 was bond with miR-129-5p, and circ-CCDC66 regulated LHX2 expression to participated in GC progression via miR-129-5p. All the findings suggested that CCDC66 could adjust LHX2 expression to promote GC progression through restraining miR-129-5p, which may provide a key strategy for GC therapy.
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CiteScore
4.30
自引率
17.20%
发文量
145
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2.3 months
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