Jingpeng Wang, Shuyuan Li, Gaofeng Zhang, Huihua Han
{"title":"七氟醚通过hsa_circ_0000231介导的miR-622抑制结直肠癌的恶性进展。","authors":"Jingpeng Wang, Shuyuan Li, Gaofeng Zhang, Huihua Han","doi":"10.1186/s40709-021-00145-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Sevoflurane (Sev), a commonly used volatile anesthetic, has been reported to inhibit the process of colorectal cancer (CRC). Circular RNAs (circRNAs) are revealed to participate in the pathogenesis of CRC. This study aims to reveal the mechanism of hsa_circ_0000231 in Sev-mediated CRC progression.</p><p><strong>Methods: </strong>The expression of hsa_circ_0000231 and microRNA-622 (miR-622) was detected by quantitative real-time polymerase chain reaction (qRT-PCR). Protein level was determined by western blot analysis. Cell proliferation was investigated by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), cell colony formation and DNA content quantitation assays. Cell apoptosis was detected by Annexin V-fluorescein isothiocyanate and propidium iodide double staining and caspase 3 activity assays. Cell migration and invasion were investigated by wound-healing and transwell invasion assays, respectively. The putative relationship between hsa_circ_0000231 and miR-622 was predicted by circular RNA Interactome online database, and identified by dual-luciferase reporter and RNA immunoprecipitation assays. The impacts of hsa_circ_0000231 on Sev-mediated tumor formation in vivo were presented by in vivo assay.</p><p><strong>Results: </strong>Hsa_circ_0000231 expression was upregulated, while miR-622 was downregulated in CRC tissues and cells compared with control groups. Sev treatment decreased hsa_circ_0000231 expression, but increased miR-622 expression in CRC cells. Sev treatment suppressed cell proliferation, migration and invasion, and induced cell apoptosis. Hsa_circ_0000231 overexpression restored Sev-mediated CRC progression in vitro. Additionally, hsa_circ_0000231 acted as a sponge of miR-622, and miR-622 inhibitors reversed the impacts of hsa_circ_0000231 silencing on CRC process. Furthermore, Sev treatment inhibited tumor growth by regulating hsa_circ_0000231 in vivo.</p><p><strong>Conclusion: </strong>Hsa_circ_0000231 attenuated Sev-aroused repression impacts on CRC development by sponging miR-622. This findings may provide an appropriate anesthetic protocol for CRC sufferers undergoing surgery.</p>","PeriodicalId":50251,"journal":{"name":"Journal of Biological Research-Thessaloniki","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2021-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s40709-021-00145-6","citationCount":"8","resultStr":"{\"title\":\"Sevoflurane inhibits malignant progression of colorectal cancer via hsa_circ_0000231-mediated miR-622.\",\"authors\":\"Jingpeng Wang, Shuyuan Li, Gaofeng Zhang, Huihua Han\",\"doi\":\"10.1186/s40709-021-00145-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Sevoflurane (Sev), a commonly used volatile anesthetic, has been reported to inhibit the process of colorectal cancer (CRC). Circular RNAs (circRNAs) are revealed to participate in the pathogenesis of CRC. This study aims to reveal the mechanism of hsa_circ_0000231 in Sev-mediated CRC progression.</p><p><strong>Methods: </strong>The expression of hsa_circ_0000231 and microRNA-622 (miR-622) was detected by quantitative real-time polymerase chain reaction (qRT-PCR). Protein level was determined by western blot analysis. Cell proliferation was investigated by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), cell colony formation and DNA content quantitation assays. Cell apoptosis was detected by Annexin V-fluorescein isothiocyanate and propidium iodide double staining and caspase 3 activity assays. Cell migration and invasion were investigated by wound-healing and transwell invasion assays, respectively. The putative relationship between hsa_circ_0000231 and miR-622 was predicted by circular RNA Interactome online database, and identified by dual-luciferase reporter and RNA immunoprecipitation assays. The impacts of hsa_circ_0000231 on Sev-mediated tumor formation in vivo were presented by in vivo assay.</p><p><strong>Results: </strong>Hsa_circ_0000231 expression was upregulated, while miR-622 was downregulated in CRC tissues and cells compared with control groups. Sev treatment decreased hsa_circ_0000231 expression, but increased miR-622 expression in CRC cells. Sev treatment suppressed cell proliferation, migration and invasion, and induced cell apoptosis. Hsa_circ_0000231 overexpression restored Sev-mediated CRC progression in vitro. Additionally, hsa_circ_0000231 acted as a sponge of miR-622, and miR-622 inhibitors reversed the impacts of hsa_circ_0000231 silencing on CRC process. Furthermore, Sev treatment inhibited tumor growth by regulating hsa_circ_0000231 in vivo.</p><p><strong>Conclusion: </strong>Hsa_circ_0000231 attenuated Sev-aroused repression impacts on CRC development by sponging miR-622. 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引用次数: 8
摘要
背景:七氟醚(Sev)是一种常用的挥发性麻醉剂,据报道可抑制结直肠癌(CRC)的发生。环状rna (circRNAs)被发现参与CRC的发病机制。本研究旨在揭示hsa_circ_0000231在sev介导的CRC进展中的机制。方法:采用实时荧光定量聚合酶链式反应(qRT-PCR)检测hsa_circ_0000231和microRNA-622 (miR-622)的表达。western blot检测蛋白水平。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)、细胞集落形成和DNA含量测定法观察细胞增殖情况。采用Annexin v -异硫氰酸荧光素和碘化丙啶双染色法和caspase 3活性测定法检测细胞凋亡。细胞迁移和侵袭分别通过创面愈合和跨井侵袭试验进行研究。hsa_circ_0000231和miR-622之间的推定关系通过环状RNA Interactome在线数据库预测,并通过双荧光素酶报告基因和RNA免疫沉淀试验进行鉴定。通过体内实验研究hsa_circ_0000231对sev介导的肿瘤形成的影响。结果:与对照组相比,Hsa_circ_0000231在结直肠癌组织和细胞中表达上调,miR-622表达下调。Sev处理降低了hsa_circ_0000231的表达,但增加了CRC细胞中miR-622的表达。Sev处理抑制细胞增殖、迁移和侵袭,诱导细胞凋亡。Hsa_circ_0000231过表达恢复了sev介导的CRC体外进展。此外,hsa_circ_0000231作为miR-622的海绵,miR-622抑制剂逆转了hsa_circ_0000231沉默对CRC过程的影响。此外,Sev治疗通过调节体内hsa_circ_0000231抑制肿瘤生长。结论:Hsa_circ_0000231通过海绵化miR-622减弱了sev引起的抑制对结直肠癌发展的影响。这一发现可能为接受手术的结直肠癌患者提供合适的麻醉方案。
Sevoflurane inhibits malignant progression of colorectal cancer via hsa_circ_0000231-mediated miR-622.
Background: Sevoflurane (Sev), a commonly used volatile anesthetic, has been reported to inhibit the process of colorectal cancer (CRC). Circular RNAs (circRNAs) are revealed to participate in the pathogenesis of CRC. This study aims to reveal the mechanism of hsa_circ_0000231 in Sev-mediated CRC progression.
Methods: The expression of hsa_circ_0000231 and microRNA-622 (miR-622) was detected by quantitative real-time polymerase chain reaction (qRT-PCR). Protein level was determined by western blot analysis. Cell proliferation was investigated by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), cell colony formation and DNA content quantitation assays. Cell apoptosis was detected by Annexin V-fluorescein isothiocyanate and propidium iodide double staining and caspase 3 activity assays. Cell migration and invasion were investigated by wound-healing and transwell invasion assays, respectively. The putative relationship between hsa_circ_0000231 and miR-622 was predicted by circular RNA Interactome online database, and identified by dual-luciferase reporter and RNA immunoprecipitation assays. The impacts of hsa_circ_0000231 on Sev-mediated tumor formation in vivo were presented by in vivo assay.
Results: Hsa_circ_0000231 expression was upregulated, while miR-622 was downregulated in CRC tissues and cells compared with control groups. Sev treatment decreased hsa_circ_0000231 expression, but increased miR-622 expression in CRC cells. Sev treatment suppressed cell proliferation, migration and invasion, and induced cell apoptosis. Hsa_circ_0000231 overexpression restored Sev-mediated CRC progression in vitro. Additionally, hsa_circ_0000231 acted as a sponge of miR-622, and miR-622 inhibitors reversed the impacts of hsa_circ_0000231 silencing on CRC process. Furthermore, Sev treatment inhibited tumor growth by regulating hsa_circ_0000231 in vivo.
Conclusion: Hsa_circ_0000231 attenuated Sev-aroused repression impacts on CRC development by sponging miR-622. This findings may provide an appropriate anesthetic protocol for CRC sufferers undergoing surgery.
期刊介绍:
Journal of Biological Research-Thessaloniki is a peer-reviewed, open access, international journal that publishes articles providing novel insights into the major fields of biology.
Topics covered in Journal of Biological Research-Thessaloniki include, but are not limited to: molecular biology, cytology, genetics, evolutionary biology, morphology, development and differentiation, taxonomy, bioinformatics, physiology, marine biology, behaviour, ecology and conservation.