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miR-495-3p 通过下调结直肠癌中的 HMGB1 来抑制细胞增殖和迁移。

miR-495-3p depresses cell proliferation and migration by downregulating HMGB1 in colorectal cancer.

机构信息

Department of Oncology, The First Affiliated Hospital of Wannan Medical College, Wuhu, 241002, China.

Department of Clinical Medicine, Wannan Medical College, Wuhu, 241002, China.

出版信息

World J Surg Oncol. 2022 Mar 30;20(1):101. doi: 10.1186/s12957-022-02500-w.

DOI:10.1186/s12957-022-02500-w
PMID:35354479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8966301/
Abstract

BACKGROUND

MicroRNAs play an important role in the genesis and progression of tumours, including colorectal cancer (CRC), which has a high morbidity and mortality rate. In this research, the role of miR-495-3p and HMGB1 in CRC was investigated.

METHODS

We performed qRT-PCR to detect the expression of miR-495-3p in colorectal cancer tissues and cell lines. Functional experiments, such as CCK-8, EdU, Transwell and apoptosis assays, were conducted to explore the effects of miR-495-3p on the proliferation, migration and apoptosis of CRC cells in vitro. Then, database prediction, dual-luciferase reporter gene assays and functional experiments verified the role of the miR-495-3p target gene HMGB1 in CRC. Finally, rescue experiments were performed to investigate whether overexpression of HMGB1 could reverse the inhibitory effect of miR-495-3p on CRC cell proliferation in vivo and in vitro.

RESULTS

miR-495-3p was downregulated in colorectal cancer tissues and cell lines, inhibited the proliferation and migration of colorectal cancer cells and promoted cell apoptosis. Database prediction and dual-luciferase reporter gene assays showed that HMGB1 was the downstream target gene of miR-495-3p. We finally demonstrated that miR-495-3p inhibited CRC cell proliferation by targeting HMGB1 in vitro and in vivo.

CONCLUSION

Our research shows that miR-495-3p inhibits the progression of colorectal cancer by downregulating the expression of HMGB1, which indicates that miR-495-3p may become a potential therapeutic target for colorectal cancer.

摘要

背景

微小 RNA 在肿瘤的发生和发展中起着重要作用,包括结直肠癌(CRC),其发病率和死亡率都很高。在这项研究中,研究了 miR-495-3p 和 HMGB1 在 CRC 中的作用。

方法

我们通过 qRT-PCR 检测结直肠癌组织和细胞系中 miR-495-3p 的表达。进行 CCK-8、EdU、Transwell 和凋亡实验等功能实验,以研究 miR-495-3p 对 CRC 细胞体外增殖、迁移和凋亡的影响。然后,通过数据库预测、双荧光素酶报告基因实验和功能实验验证了 miR-495-3p 靶基因 HMGB1 在 CRC 中的作用。最后,进行了挽救实验,以研究 HMGB1 的过表达是否可以逆转 miR-495-3p 对 CRC 细胞在体内和体外增殖的抑制作用。

结果

miR-495-3p 在结直肠癌组织和细胞系中下调,抑制结直肠癌细胞的增殖和迁移,促进细胞凋亡。数据库预测和双荧光素酶报告基因实验表明,HMGB1 是 miR-495-3p 的下游靶基因。我们最终证明 miR-495-3p 通过靶向 HMGB1 在体外和体内抑制 CRC 细胞增殖。

结论

我们的研究表明,miR-495-3p 通过下调 HMGB1 的表达抑制结直肠癌的进展,这表明 miR-495-3p 可能成为结直肠癌的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/369184c51489/12957_2022_2500_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/3c11497a5b54/12957_2022_2500_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/cd1388a3f5eb/12957_2022_2500_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/e551329c48b5/12957_2022_2500_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/369184c51489/12957_2022_2500_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/3c11497a5b54/12957_2022_2500_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/cd1388a3f5eb/12957_2022_2500_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/e551329c48b5/12957_2022_2500_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d8/8966301/369184c51489/12957_2022_2500_Fig5_HTML.jpg

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