hsa-mir-145-5p调控结直肠癌中msln表达的作用

IF 2.6 4区 医学 Q3 CELL BIOLOGY Analytical Cellular Pathology Pub Date : 2022-01-01 DOI:10.1155/2022/5587084
Junhua Li, Bulin Baila, Tian Xiang Xu, Jiang Song, Su Rina, Ji Wu, Tegexibaiyin Wang
{"title":"hsa-mir-145-5p调控结直肠癌中msln表达的作用","authors":"Junhua Li,&nbsp;Bulin Baila,&nbsp;Tian Xiang Xu,&nbsp;Jiang Song,&nbsp;Su Rina,&nbsp;Ji Wu,&nbsp;Tegexibaiyin Wang","doi":"10.1155/2022/5587084","DOIUrl":null,"url":null,"abstract":"<p><p>Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contributed with the prognosis of CRC. Microarray technology was used, and 179 miRNAs were screened out with significantly altered expression in CRC tissues compared with adjacent tissues. The expression of mir-145-5p in tumor tissues was 3.48 times lower than that in normal tissues. Using bioinformatics technology and network resource prediction, we found that mir-145-5p had a potential target gene relationship with <i>msln</i> gene. Then, qRT-PCR was used to validate the expression level of mir-145-5p and <i>msln</i> mRNA in CRC and paracancerous tissues. The results showed that <i>msln</i> mRNA was higher than in normal tissues, while mir-145-5p was lower, with statistically significant difference (<i>P</i> < 0.01, <i>n</i> = 3). Furthermore, the expression of msln protein in CRC and normal colorectal tissues was detected by protein mass spectrometry (MRM) (<i>n</i> = 3) and immunohistochemistry in a total case of 30 colorectal cancer tissues and normal tissues. Result showed that the positive expression of msln in CRC was higher than that in normal colorectal tissues, 1.38<i>e</i>-6 and 1.89<i>e</i>-6, respectively (<i>P</i> < 0.01, <i>n</i> = 3). Furthermore, in 48 h RTCA real-time monitoring experiment, mir-145-5p showed inhibitory effect on the proliferation of colo320 cells stimulated by msln. This study demonstrated that <i>msln</i> is a target gene of mir-145-5p in CRC. Besides, mir-145-5p negatively regulates the proliferation of CRC colo320 cells through downregulating <i>msln</i> gene expression in CRC colo320 cells.</p>","PeriodicalId":49326,"journal":{"name":"Analytical Cellular Pathology","volume":"2022 ","pages":"5587084"},"PeriodicalIF":2.6000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941573/pdf/","citationCount":"1","resultStr":"{\"title\":\"Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma.\",\"authors\":\"Junhua Li,&nbsp;Bulin Baila,&nbsp;Tian Xiang Xu,&nbsp;Jiang Song,&nbsp;Su Rina,&nbsp;Ji Wu,&nbsp;Tegexibaiyin Wang\",\"doi\":\"10.1155/2022/5587084\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contributed with the prognosis of CRC. Microarray technology was used, and 179 miRNAs were screened out with significantly altered expression in CRC tissues compared with adjacent tissues. The expression of mir-145-5p in tumor tissues was 3.48 times lower than that in normal tissues. Using bioinformatics technology and network resource prediction, we found that mir-145-5p had a potential target gene relationship with <i>msln</i> gene. Then, qRT-PCR was used to validate the expression level of mir-145-5p and <i>msln</i> mRNA in CRC and paracancerous tissues. The results showed that <i>msln</i> mRNA was higher than in normal tissues, while mir-145-5p was lower, with statistically significant difference (<i>P</i> < 0.01, <i>n</i> = 3). Furthermore, the expression of msln protein in CRC and normal colorectal tissues was detected by protein mass spectrometry (MRM) (<i>n</i> = 3) and immunohistochemistry in a total case of 30 colorectal cancer tissues and normal tissues. Result showed that the positive expression of msln in CRC was higher than that in normal colorectal tissues, 1.38<i>e</i>-6 and 1.89<i>e</i>-6, respectively (<i>P</i> < 0.01, <i>n</i> = 3). Furthermore, in 48 h RTCA real-time monitoring experiment, mir-145-5p showed inhibitory effect on the proliferation of colo320 cells stimulated by msln. This study demonstrated that <i>msln</i> is a target gene of mir-145-5p in CRC. Besides, mir-145-5p negatively regulates the proliferation of CRC colo320 cells through downregulating <i>msln</i> gene expression in CRC colo320 cells.</p>\",\"PeriodicalId\":49326,\"journal\":{\"name\":\"Analytical Cellular Pathology\",\"volume\":\"2022 \",\"pages\":\"5587084\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941573/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Cellular Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/2022/5587084\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Cellular Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2022/5587084","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

结直肠癌(Colorectal cancer, CRC)是世界上最常见的胃肠道肿瘤之一,其发病率在包括中国在内的世界各国都呈上升趋势。近年来的研究数据显示,一些mirna在癌组织中存在差异表达,其表达与结直肠癌的预后密切相关。使用微阵列技术,筛选出179个在结直肠癌组织中与邻近组织相比表达显著改变的mirna。mir-145-5p在肿瘤组织中的表达比正常组织低3.48倍。利用生物信息学技术和网络资源预测,我们发现mir-145-5p与msln基因存在潜在的靶基因关系。然后采用qRT-PCR验证mir-145-5p和msln mRNA在结直肠癌和癌旁组织中的表达水平。结果显示,msln mRNA水平高于正常组织,mir-145-5p水平低于正常组织,差异有统计学意义(P < 0.01, n = 3)。此外,在共30例结直肠癌组织和正常组织中,采用蛋白质谱(MRM) (n = 3)和免疫组化检测msln蛋白在结直肠癌组织和正常组织中的表达。结果显示,msln在结直肠癌中的阳性表达高于正常结直肠癌组织,分别为1.38e-6和1.89e-6 (P < 0.01, n = 3)。此外,在48 h RTCA实时监测实验中,mir-145-5p对msln刺激的结肠320细胞增殖有抑制作用。本研究证实msln是CRC中mir-145-5p的靶基因。此外,mir-145-5p通过下调CRC col320细胞中msln基因的表达,负向调控CRC col320细胞的增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Effects of hsa-mir-145-5p on the Regulation of msln Expression in Colorectal Adenocarcinoma.

Colorectal cancer (CRC) is one of the most common gastrointestinal cancers in the world, and its incidence is increasing all over the world including China. In recent years, research data show that some miRNAs are differentially expressed in cancer tissues, and their expression is closely contributed with the prognosis of CRC. Microarray technology was used, and 179 miRNAs were screened out with significantly altered expression in CRC tissues compared with adjacent tissues. The expression of mir-145-5p in tumor tissues was 3.48 times lower than that in normal tissues. Using bioinformatics technology and network resource prediction, we found that mir-145-5p had a potential target gene relationship with msln gene. Then, qRT-PCR was used to validate the expression level of mir-145-5p and msln mRNA in CRC and paracancerous tissues. The results showed that msln mRNA was higher than in normal tissues, while mir-145-5p was lower, with statistically significant difference (P < 0.01, n = 3). Furthermore, the expression of msln protein in CRC and normal colorectal tissues was detected by protein mass spectrometry (MRM) (n = 3) and immunohistochemistry in a total case of 30 colorectal cancer tissues and normal tissues. Result showed that the positive expression of msln in CRC was higher than that in normal colorectal tissues, 1.38e-6 and 1.89e-6, respectively (P < 0.01, n = 3). Furthermore, in 48 h RTCA real-time monitoring experiment, mir-145-5p showed inhibitory effect on the proliferation of colo320 cells stimulated by msln. This study demonstrated that msln is a target gene of mir-145-5p in CRC. Besides, mir-145-5p negatively regulates the proliferation of CRC colo320 cells through downregulating msln gene expression in CRC colo320 cells.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Analytical Cellular Pathology
Analytical Cellular Pathology ONCOLOGY-CELL BIOLOGY
CiteScore
4.90
自引率
3.10%
发文量
70
审稿时长
16 weeks
期刊介绍: Analytical Cellular Pathology is a peer-reviewed, Open Access journal that provides a forum for scientists, medical practitioners and pathologists working in the area of cellular pathology. The journal publishes original research articles, review articles, and clinical studies related to cytology, carcinogenesis, cell receptors, biomarkers, diagnostic pathology, immunopathology, and hematology.
期刊最新文献
Shikonin Induces Autophagy and Apoptosis in Esophageal Cancer EC9706 Cells by Regulating the AMPK/mTOR/ULK Axis. Hippo Signaling Pathway in Colorectal Cancer: Modulation by Various Signals and Therapeutic Potential. Exosomal PDL1 Suppresses the Anticancer Activity of CD8+ T Cells in Hepatocellular Carcinoma. AZD8055 Is More Effective Than Rapamycin in Inhibiting Proliferation and Promoting Mitochondrial Clearance in Erythroid Differentiation. Malignant Transformation of Normal Oral Tissue to Dysplasia and Early Oral Squamous Cell Carcinoma: An In Silico Transcriptomics Approach.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1