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Mini Rev Med Chem. 2024;24(18):1685-1700. doi: 10.2174/0113895575284780240327103039.
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Biological roles of SLC16A1-AS1 lncRNA and its clinical impacts in tumors.SLC16A1-AS1长链非编码RNA的生物学作用及其在肿瘤中的临床影响
Cancer Cell Int. 2024 Mar 30;24(1):122. doi: 10.1186/s12935-024-03285-6.
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Colorectal Cancer: From Risk Factors to Oncogenesis.结直肠癌:从风险因素到致癌机制。
Medicina (Kaunas). 2023 Sep 12;59(9):1646. doi: 10.3390/medicina59091646.
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Circular RNA PGPEP1 induces colorectal cancer malignancy and immune escape.环状 RNA PGPEP1 诱导结直肠癌细胞恶性转化和免疫逃逸。
Cell Cycle. 2023 Jul-Aug;22(14-16):1743-1758. doi: 10.1080/15384101.2023.2225923. Epub 2023 Jul 9.
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MAPKAPK5-AS1/miR-515-5p/CAB39 Axis Contributes to Non-small Cell Lung Cancer Cell Proliferation and Migration.MAPKAPK5-AS1/miR-515-5p/CAB39 轴促进非小细胞肺癌细胞的增殖和迁移。
Mol Biotechnol. 2023 Nov;65(11):1887-1897. doi: 10.1007/s12033-023-00654-w. Epub 2023 Mar 3.
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Deep top-down proteomics revealed significant proteoform-level differences between metastatic and nonmetastatic colorectal cancer cells.深度自上而下的蛋白质组学揭示了转移性和非转移性结直肠癌细胞之间在蛋白质水平上的显著差异。
Sci Adv. 2022 Dec 21;8(51):eabq6348. doi: 10.1126/sciadv.abq6348.
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Analysis of the subcellular location of lncRNA SLC16A1-AS1 and its interaction with premature miR-5088-5p in oral squamous cell carcinoma.口腔鳞状细胞癌中lncRNA SLC16A1-AS1的亚细胞定位及其与前体miR-5088-5p相互作用的分析
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Clinical management of metastatic colorectal cancer in the era of precision medicine.精准医学时代转移性结直肠癌的临床管理。
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Promoter methylation-regulated miR-148a-3p inhibits lung adenocarcinoma (LUAD) progression by targeting MAP3K9.启动子甲基化调控的miR-148a-3p通过靶向MAP3K9抑制肺腺癌(LUAD)进展。
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Overexpression of lncRNA SLC16A1-AS1 Suppresses the Growth and Metastasis of Breast Cancer the miR-552-5p/WIF1 Signaling Pathway.长链非编码RNA SLC16A1-AS1的过表达通过miR-552-5p/WIF1信号通路抑制乳腺癌的生长和转移。
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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.

DOI:10.62347/ABOI7514
PMID:39659936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11626282/
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。