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长链非编码RNA SLC16A1-AS1通过靶向miR-515-5p调控丝裂原活化蛋白激酶激酶激酶9(MAP3K9)的表达,参与结直肠癌的发生和发展。

LncRNA SLC16A1-AS1 participates in the initiation and progression of colorectal cancer by regulating MAP3K9 expression through targeting miR-515-5p.

作者信息

Xu Wanxing, Bi Suzhen, Xing Meichun

机构信息

Department of Laboratory Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine Shanghai 201620, China.

Precision Research Center for Refractory Diseases, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine Shanghai 201620, China.

出版信息

Am J Cancer Res. 2024 Nov 25;14(11):5539-5550. doi: 10.62347/ABOI7514. eCollection 2024.

Abstract

OBJECTIVE

To investigate the role of long non-coding RNA (lncRNA) SLC16A1-AS1 in the initiation and progression of colorectal cancer (CRC).

METHODS

Cell viability was tested using Cell Counting Kit-8 (CCK-8). Cell invasion and migration were evaluated using Transwell assays, and apoptosis was determined by flow cytometry. Gene expression was tested by qRT-PCR or Western blot. The targeting relationship between miR-515-5p and MAP3K9 was verified using bioinformatics tools, RNA immunoprecipitation (RIP) experiments, and dual-luciferase reporter assays.

RESULTS

Both lncRNA SLC16A1-AS1 and MAP3K9 were upregulated in CRC cells, while miR-515-5p expression was downregulated. Overexpression of miR-515-5p and silencing of lncRNA SLC16A1-AS1 inhibited CRC cell proliferation, suppressed cell invasion and migration, and promoted cell apoptosis. The targeting relationship between lncRNA SLC16A1-AS1 and miR-515-5p, as well as between MAP3K9 and miR-515-5p, were confirmed by bioinformatics, RIP assays, and luciferase reporter assays.

CONCLUSION

lncRNA SLC16A1-AS1 contributes to the initiation and progression of CRC by modulating miR-515-5p to regulate MAP3K9 expression, providing potential insights for CRC treatment.

摘要

目的

探讨长链非编码RNA(lncRNA)SLC16A1-AS1在结直肠癌(CRC)发生发展中的作用。

方法

使用细胞计数试剂盒-8(CCK-8)检测细胞活力。采用Transwell实验评估细胞侵袭和迁移能力,通过流式细胞术检测细胞凋亡情况。采用qRT-PCR或蛋白质免疫印迹法检测基因表达。利用生物信息学工具、RNA免疫沉淀(RIP)实验和双荧光素酶报告基因检测验证miR-515-5p与MAP3K9之间的靶向关系。

结果

lncRNA SLC16A1-AS1和MAP3K9在CRC细胞中均上调,而miR-515-5p表达下调。miR-515-5p过表达和lncRNA SLC16A1-AS1沉默可抑制CRC细胞增殖,抑制细胞侵袭和迁移,并促进细胞凋亡。通过生物信息学、RIP实验和荧光素酶报告基因检测证实了lncRNA SLC16A1-AS1与miR-515-5p以及MAP3K9与miR-515-5p之间的靶向关系。

结论

lncRNA SLC16A1-AS1通过调控miR-515-5p来调节MAP3K9表达,从而促进CRC的发生发展,为CRC治疗提供了潜在的见解。

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