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长链非编码 RNA CBR3 反义 RNA 1 在结直肠癌中下调,并抑制 miR-29a 介导的细胞迁移和侵袭。

Long Non-coding RNA CBR3 Antisense RNA 1 is Downregulated in Colorectal Cancer and Inhibits miR-29a-Mediated Cell Migration and Invasion.

机构信息

Department of Gastroenterology, EZhou Central Hospital, No. 9, Wenxing Road, Echeng District, Ezhou, 436000, Hubei, People's Republic of China.

出版信息

Mol Biotechnol. 2022 Jul;64(7):773-779. doi: 10.1007/s12033-021-00444-2. Epub 2022 Feb 2.

Abstract

Although CBR3 Antisense RNA 1 (CBR3-AS1) has been characterized as an oncogenic long non-coding RNA (lncRNA) in several cancers, a recent study reported the downregulation of CBR3-AS1 in colorectal cancer (CRC). Therefore, we analyzed its role in CRC. CBR3-AS1 and microRNA-29a (miR-29a) expression in tissue samples from CRC patients were analyzed by RT-qPCR. The interaction between CBR3-AS1 and miR-29a was predicted by IntaRNA and validated by RNA pull-down assay. The location of CBR3-AS1 was analyzed by nuclear fractionation assay. CBR3-AS1 overexpression was performed to analyze its role in miR-29a expression. The roles of CBR3-AS1 and miR-29a in CRC cell migration and invasion were analyzed by Transwell assay. CBR3-AS1 was downregulated, and miR-29a was upregulated in CRC. CBR3-AS1 and miR-29a directly interacted with each other. CBR3-AS1 was localized in both nucleus and cytoplasm fractions. CBR3-AS1 overexpression failed to alter miR-29a expression but reduced its enhancing effects on cell invasion and migration. CBR3-AS1 is downregulated in CRC and inhibits miR-29a-mediated cell migration and invasion by sponging miR-29a.

摘要

尽管 CBR3 反义 RNA1(CBR3-AS1)已被证实为多种癌症中的致癌长非编码 RNA(lncRNA),但最近的一项研究报告称其在结直肠癌(CRC)中下调。因此,我们分析了其在 CRC 中的作用。通过 RT-qPCR 分析了 CRC 患者组织样本中的 CBR3-AS1 和 microRNA-29a(miR-29a)表达。通过 IntaRNA 预测 CBR3-AS1 和 miR-29a 之间的相互作用,并通过 RNA 下拉测定验证。通过核分馏测定分析 CBR3-AS1 的位置。通过转染 CBR3-AS1 过表达来分析其对 miR-29a 表达的作用。通过 Transwell 测定分析 CBR3-AS1 和 miR-29a 在 CRC 细胞迁移和侵袭中的作用。CRC 中 CBR3-AS1 下调,miR-29a 上调。CBR3-AS1 和 miR-29a 直接相互作用。CBR3-AS1 定位于核和胞质部分。CBR3-AS1 过表达未能改变 miR-29a 的表达,但降低了其对细胞侵袭和迁移的增强作用。CBR3-AS1 在 CRC 中下调,并通过海绵吸附 miR-29a 抑制 miR-29a 介导的细胞迁移和侵袭。

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