Circular RNA hsa_circ_0005939 Regulates UHRF1BP1L Expression by Targeting miR-4693-3p to Promote Colorectal Cancer Progression.

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hua Ge, Yan Yan, Haomin Wang, Jun Bian, Zhilong Deng, Xian Su, Kaiyuan Luo, Jianfeng Bin
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Abstract

Introduction: Colorectal cancer (CRC) is the second most common and fatal cancer in China. circRNAs are different expressed between tumor and non-tumor tissues, and they are proved to be correlated with tumorigenesis and cancer progression.

Objective: We aimed to explore the biological and molecular function of hsa_circ_0005939 in CRC.

Methods: We collected and compared ten CRC tissues and four noncancerous tissues and performed circRNA sequencing. We investigated the hsa_circ_0005939 expression in fresh tissues from CRC and adjacent tissues by qPCR. Meanwhile, functional roles of hsa_circ_0005939 in CRC cells were explored by CCK-8, colony formation, wounding healing, cell apoptosis and western blot assays. RNA-FISH was used to confirm the cellular distribution of hsa_circ_0005939. Bioinformatic prediction and luciferase reporter assay were used to determine the mechanisms of hsa_circ_0005939.

Results: Our results indicated that hsa_circ_0005939 was up-regulated in CRC tissues and cells. Up-regulation of hsa_circ_0005939 was associated with the occurrence and the number of lymph node metastasis of CRC. Hsa_circ_0005939 down-regulation inhibited cell proliferation, increased cell apoptosis and caused G2 phase arrest of CRC cells. Mechanistically, luciferase assay revealed that hsa_circ_0005939 acts as a molecular sponge for miR-4693-3p and then enhanced Ubiquitin Like With PHD And Ring Finger Domains 1 binding protein 1 like (UHRF1BP1L) expression.

Conclusion: Our findings indicated an oncogenic role of hsa_circ_0005939 in CRC, and it enhanced malignant phenotypes of CRC cells through miR-4693-3p/UHRF1BP1L axis. Our study may offer promising biomarkers and therapeutic targets for CRC.

环状 RNA hsa_circ_0005939 通过靶向 miR-4693-3p 来调控 UHRF1BP1L 的表达,从而促进结直肠癌的进展。
导读:大肠癌(CRC)是中国第二大常见和致命癌症:circRNAs在肿瘤组织和非肿瘤组织中的表达不同,被证实与肿瘤的发生和发展相关:目的:探讨 hsa_circ_0005939 在 CRC 中的生物学和分子功能:方法:我们收集并比较了 10 例 CRC 组织和 4 例非癌组织,并进行了 circRNA 测序。通过 qPCR 方法检测了 hsa_circ_0005939 在 CRC 和邻近组织新鲜组织中的表达。同时,通过CCK-8、菌落形成、创伤愈合、细胞凋亡和Western印迹检测,探讨了hsa_circ_0005939在CRC细胞中的功能作用。RNA-FISH 被用来确认 hsa_circ_0005939 在细胞中的分布。通过生物信息学预测和荧光素酶报告实验确定了 hsa_circ_0005939 的作用机制:结果表明,hsa_circ_0005939在CRC组织和细胞中上调。hsa_circ_0005939的上调与CRC淋巴结转移的发生和数量有关。下调 Hsa_circ_0005939 可抑制 CRC 细胞增殖、增加细胞凋亡并导致 G2 期停滞。荧光素酶分析表明,hsa_circ_0005939可作为miR-4693-3p的分子海绵,进而增强泛素结合蛋白1(Ubiquitin Like With PHD And Ring Finger Domains 1 binding protein 1 like,UHRF1BP1L)的表达:我们的研究结果表明,hsa_circ_0005939 在 CRC 中具有致癌作用,它通过 miR-4693-3p/UHRF1BP1L 轴增强了 CRC 细胞的恶性表型。我们的研究可能会为 CRC 提供有前景的生物标记物和治疗靶点。
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来源期刊
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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