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首页> 外文期刊>European review for medical and pharmacological sciences. >MiR-340-5p is a potential prognostic indicator of colorectal cancer and modulates ANXA3
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MiR-340-5p is a potential prognostic indicator of colorectal cancer and modulates ANXA3

机译:MiR-340-5p是结直肠癌的潜在预后指标,可调节ANXA3

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OBJECTIVE: MicroRNAs (miRNAs) are increasingly recognized as oncogenes or tumor suppressors in colorectal cancer (CRC). The aim of this study was to explore the expression and functions of miR-340-5p in CRC. PATIENTS AND METHODS: The expression of miR-340-5p in CRC tissues and cell lines was detected by quantitative RT-PCR. Associations of miR-340-5p expression with clinicopathological factors and overall survival (OS) and progression-free survival (PFS) were statistically evaluated. Luciferase assay, RT-PCR, and Western blot were performed to verify the precise target of miR-340-5p. MTT assay, colony formation and transwell assay were performed to determine the proliferation, migration and invasion, respectively. RESULTS: Our results showed that miR-340-5p was significantly down-regulated in CRC tissues and cell lines, and was associated with histological grade (p=0.020), lymph nodes metastasis (p=0.003) and TNM stage (p=0.007). Furthermore, Kaplan-Meier and log-rank tests revealed that patients with low expression of miR-340-5p had a shorter OS (p=0.0110) and PFS (p=0.0032) than those with high expression of miR-340-5p. We further validated Annexin A3 (ANXA3) was a direct target of miR-340-5p in CRC. The functional assay showed that up-regulation of miR-340-5p or down-regulation of ANXA3 can both inhibit CRC cell proliferation, migration, and invasion. Besides, the re-expression of ANXA3 reversed the miR-340-5p induced suppression of cell proliferation, migration and invasion. CONCLUSIONS: Our data demonstrated that miR-340-5p exerted its tumor-suppressive function by directly targeting ANXA3 in CRC, suggesting that miR-340-5p might represent a novel prognostic biomarker and therapeutic target for CRC.
机译:目的:MicroRNA(miRNA)在大肠癌(CRC)中被越来越多地认为是癌基因或抑癌基因。这项研究的目的是探索miR-340-5p在CRC中的表达和功能。病人和方法:通过定量RT-PCR检测miR-340-5p在CRC组织和细胞系中的表达。对miR-340-5p表达与临床病理因素以及总生存期(OS)和无进展生存期(PFS)的关联进行统计评估。进行荧光素酶测定,RT-PCR和蛋白质印迹以验证miR-340-5p的精确靶标。进行MTT测定,菌落形成和transwell测定,分别测定增殖,迁移和侵袭。结果:我们的结果表明,miR-340-5p在CRC组织和细胞系中显着下调,并与组织学分级(p = 0.020),淋巴结转移(p = 0.003)和TNM分期(p = 0.007)相关)。此外,Kaplan-Meier和对数秩检验显示,与miR-340-5p高表达患者相比,miR-340-5p低表达患者的OS(p = 0.0110)和PFS(p = 0.0032)较短。我们进一步证实膜联蛋白A3(ANXA3)是CRC中miR-340-5p的直接靶标。功能测定表明,miR-340-5p的上调或ANXA3的下调均可以抑制CRC细胞的增殖,迁移和侵袭。此外,ANXA3的重新表达逆转了miR-340-5p诱导的细胞增殖,迁移和侵袭抑制。结论:我们的数据表明,miR-340-5p通过直接靶向CRC中的ANXA3发挥其肿瘤抑制功能,表明miR-340-5p可能代表了CRC的新型预后生物标志物和治疗靶标。

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