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长链非编码RNA CTBP1-DT作为调节结直肠癌细胞功能的潜在治疗靶点的研究。

Research on lncRNA CTBP1-DT as a potential therapeutic target to regulate cell function in colorectal cancer.

作者信息

Fan Ruizhi, Xu Teng, Kuang Yuting

机构信息

Department of Gastrointestinal Surgery, The First Affiliated Hospital of Soochow University, No.188, Shizi Street, Suzhou, 215006, Jiangsu, China.

Department of Gastrointestinal Surgery, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China.

出版信息

Discov Oncol. 2024 Jun 12;15(1):225. doi: 10.1007/s12672-024-01085-y.


DOI:10.1007/s12672-024-01085-y
PMID:38864997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11169288/
Abstract

BACKGROUND: Colorectal cancer, which originates from the human colon or rectum, is one of the leading causes of death worldwide. Timely diagnosis and interventional therapy can significantly improve the prognostic survival of colorectal cancer patients, making regular screening and early detection essential. AIM: To investigate the regulatory function of lncRNA CTBP1-DT (CTBP1-DT) on colorectal cancer cells and to assess its diagnostic significance. METHODS: A total of 102 patients with colorectal cancer and 92 healthy individuals were selected. The levels of CTBP1-DT and microRNA-30a-5p (miR-30a-5p) in serum and cell samples of the above subjects were compared by RT-qPCR. The effects of CTBP1-DT and miR-30a-5p dysregulation on the biological functions of colorectal cancer cells were analyzed via CCK-8, flow cytometry and Transwell assays. In addition, the ability of CTBP1-DT and miR-30a-5p to early identify colorectal cancer patients was determined through ROC curve. RESULTS: Serum CTBP1-DT was elevated in patients with colorectal cancer, which was obviously higher than in healthy controls. The expression of serum miR-30a-5p was downregulated in colorectal cancer. Both CTBP1-DT and miR-30a-5p have the value of distinguishing colorectal cancer, and the combined diagnostic ability is higher. Knockdown of CTBP1-DT directly targeted miR-30a-5p to repress cell activity and metastatic ability, whereas deregulation of miR-30a-5p eliminated the above inhibitory effects. CONCLUSION: Overexpression of CTBP1-DT has a certain application potential in the diagnosis of colorectal cancer and may be a therapeutic target for colorectal cancer.

摘要

背景:结直肠癌起源于人类结肠或直肠,是全球主要的死亡原因之一。及时诊断和介入治疗可显著提高结直肠癌患者的预后生存率,因此定期筛查和早期发现至关重要。 目的:探讨长链非编码RNA CTBP1-DT(CTBP1-DT)对结直肠癌细胞的调控作用,并评估其诊断意义。 方法:选取102例结直肠癌患者和92例健康个体。采用RT-qPCR比较上述受试者血清和细胞样本中CTBP1-DT和微小RNA-30a-5p(miR-30a-5p)的水平。通过CCK-8、流式细胞术和Transwell实验分析CTBP1-DT和miR-30a-5p失调对结直肠癌细胞生物学功能的影响。此外,通过ROC曲线确定CTBP1-DT和miR-30a-5p早期识别结直肠癌患者的能力。 结果:结直肠癌患者血清CTBP1-DT升高,明显高于健康对照组。结直肠癌患者血清miR-30a-5p表达下调。CTBP1-DT和miR-30a-5p均具有区分结直肠癌的价值,联合诊断能力更高。敲低CTBP1-DT直接靶向miR-30a-5p以抑制细胞活性和转移能力,而miR-30a-5p失调则消除了上述抑制作用。 结论:CTBP1-DT的过表达在结直肠癌诊断中具有一定的应用潜力,可能是结直肠癌的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/f7ca85479377/12672_2024_1085_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/6e0c3aba0cdd/12672_2024_1085_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/f49922bf516c/12672_2024_1085_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/f7ca85479377/12672_2024_1085_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/6e0c3aba0cdd/12672_2024_1085_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/f49922bf516c/12672_2024_1085_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4422/11169288/f7ca85479377/12672_2024_1085_Fig3_HTML.jpg

相似文献

[1]
Research on lncRNA CTBP1-DT as a potential therapeutic target to regulate cell function in colorectal cancer.

Discov Oncol. 2024-6-12

[2]
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[3]
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[4]
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[6]
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Int J Mol Sci. 2020-10-3

[7]
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J Cell Mol Med. 2019-3-25

[8]
MiR-30a-5p Suppresses Tumor Metastasis of Human Colorectal Cancer by Targeting ITGB3.

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[9]
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Oncol Lett. 2021-4

[10]
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本文引用的文献

[1]
Sparassis latifolia and exercise training as complementary medicine mitigated the 5-fluorouracil potent side effects in mice with colorectal cancer: bioinformatics approaches, novel monitoring pathological metrics, screening signatures, and innovative management tactic.

Cancer Cell Int. 2024-4-18

[2]
Identify CTBP1-DT as an immunological biomarker that promotes lipid synthesis and apoptosis resistance in KIRC.

Gene. 2024-7-1

[3]
Unveiling the role of miR-137-3p/miR-296-5p/SERPINA3 signaling in colorectal cancer progression: integrative analysis of gene expression profiles and in vitro studies.

BMC Med Genomics. 2023-12-12

[4]
Types of Cell Death from a Molecular Perspective.

Biology (Basel). 2023-11-13

[5]
System biology analysis to develop diagnostic biomarkers, monitoring pathological indexes, and novel therapeutic approaches for immune targeting based on maggot bioactive compounds and polyphenolic cocktails in mice with gastric cancer.

Environ Res. 2023-12-1

[6]
The DDUP protein encoded by the DNA damage-induced CTBP1-DT lncRNA confers cisplatin resistance in ovarian cancer.

Cell Death Dis. 2023-8-26

[7]
Natural Products Treat Colorectal Cancer by Regulating miRNA.

Pharmaceuticals (Basel). 2023-8-9

[8]
CSK-mediated signalling by integrins in cancer.

Front Cell Dev Biol. 2023-7-7

[9]
MiR-30a-5p Enhances Cisplatin Sensitivity by Downregulating RIF1 in Ovarian Cancer.

Ann Clin Lab Sci. 2023-5

[10]
Retrospective efficacy analysis of olaparib combined with bevacizumab in the treatment of advanced colorectal cancer.

World J Gastrointest Surg. 2023-5-27

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