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hsa_circRNA_103809 通过 miR-532-3p/FOXO4 轴调控结直肠癌细胞的增殖和迁移。

Hsa_circRNA_103809 regulated the cell proliferation and migration in colorectal cancer via miR-532-3p / FOXO4 axis.

机构信息

Department of General Surgery, The Affiliated Hospital of Nantong University, Nantong, Jiangsu, 226000, PR China.

Department of Emergency Surgery, The Affiliated Hospital of Nantong University, Nantong, Jiangsu, 226000, PR China.

出版信息

Biochem Biophys Res Commun. 2018 Oct 28;505(2):346-352. doi: 10.1016/j.bbrc.2018.09.073. Epub 2018 Sep 22.

Abstract

Circular RNAs(circRNAs) are a class of non-coding RNAs that are widely expressed in a variety of cell species. The role they play in cancers is poorly understood, especially in colorectal cancer (CRC). Hsa_circRNA_103809 (hsa_circ_0072088, circZFR)has been demonstrated to be lowly expressed in colorectal cancer tissues and is associated with stage and lymph node metastasis of cancer tissues. Real-time quantitative PCR (qRT-PCR) was used to verify the relationship of hsa_circRNA_103809 between colorectal cancer and paired adjacent tissue in clinical tissue samples. Then, the proliferative capacity, migration ability, cell cycle, and apoptosis were measured using wound-healing assay, CCK8, transwell assay, flow cytometry, and the like, when hsa_circRNA_103809 expression in SW620 and COCA-2. The qRT-PCR, western bolt and other experiments verify that the expression of hsa_circRNA_103809 can regulate the expression of miR-532-3P and FOXO4. Hsa_circRNA_103809 was found to be significantly down regulated in CRC tissues and cell lines and compared with paired adjacent non-tumorous tissues and normal FHC cells. Hsa_circRNA_103809 participates in the regulation of biological functions through the miR-532-3P/FOXO4 axis in the CRC. Hsa_circRNA_103809 may be a potential novel gene target for the diagnosis and treatment of CRC.

摘要

环状 RNA(circRNAs) 是一类广泛存在于多种细胞物种中的非编码 RNA。它们在癌症中的作用尚未得到充分理解,特别是在结直肠癌 (CRC) 中。研究表明,hsa_circRNA_103809 (hsa_circ_0072088, circZFR) 在结直肠癌组织中低表达,并与肿瘤组织的分期和淋巴结转移相关。实时定量 PCR (qRT-PCR) 用于验证临床组织样本中 hsa_circRNA_103809 与结直肠癌及其配对相邻组织之间的关系。然后,通过划痕愈合试验、CCK8、Transwell 试验、流式细胞术等方法测量 SW620 和 COCA-2 中 hsa_circRNA_103809 表达时的增殖能力、迁移能力、细胞周期和凋亡。qRT-PCR、western bolt 等实验验证了 hsa_circRNA_103809 表达可以调节 miR-532-3P 和 FOXO4 的表达。研究发现,hsa_circRNA_103809 在 CRC 组织和细胞系中明显下调,与配对的相邻非肿瘤组织和正常 FHC 细胞相比。hsa_circRNA_103809 通过 miR-532-3P/FOXO4 轴参与 CRC 中生物功能的调节。hsa_circRNA_103809 可能是 CRC 诊断和治疗的潜在新型基因靶点。

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