CCR6 promotes liver metastasis of colorectal cancer through epithelial-mesenchymal transition

Hailing Zhang, Juanfang Li, Xiaoqing Li, Linjie Shi, Yuan-fei Li
{"title":"CCR6 promotes liver metastasis of colorectal cancer through epithelial-mesenchymal transition","authors":"Hailing Zhang, Juanfang Li, Xiaoqing Li, Linjie Shi, Yuan-fei Li","doi":"10.3760/CMA.J.ISSN.1673-422X.2020.01.005","DOIUrl":null,"url":null,"abstract":"Objective \nTo detect the expressions of chemokine receptor 6 (CCR6), CC chemokine ligand 20 (CCL20) E-cadherin and vimentin in tissues of colorectal cancer and their paired liver metastases, and to investigate the possible mechanism of CCR6 in liver metastasis of colorectal cancer. \n \n \nMethods \nA total of 62 cases (54 cases of colon cancer and 8 cases of rectal cancer) of primary colorectal adenocarcinoma resection with wax lumps were selected from the First Hospital of Shanxi Medical University and Shanxi Oncology Hospital from 2009 to 2017 with complete data, including 20 samples of colorectal cancer resection with liver metastasis during the same period. The expressions of CCR6, CCL20, E-cadherin and vimentin in colorectal cancer and liver metastases tissues were detected by immunohistochemistry, and the relationships between the expressions of CCR6, E-cadherin and vimentin and the clinicopathological features of patients were analyzed. Logistic multivariate regression was used to analyze the relationship between liver metastasis and clinicopathological features, CCR6, E-cadherin and vimentin. Spearman correlation was used to analyze the correlations between CCR6 and E-cadherin and vimentin. \n \n \nResults \nThe positive expression rate of CCR6 in colorectal cancer tissues was 66.1% (41/62), 85.0% (17/20) in colorectal cancer with liver metastasis and 70.0% (14/20) in liver metastasis tissues. The positive expression rate of CCL20 in colorectal cancer tissues was 83.9% (52/62), 90.0% (18/20) in colorectal cancer with liver metastasis and 90.0% (18/20) in liver metastasis tissues. The positive expression rate of E-cadherin in colorectal cancer tissues was 67.7% (42/62), 50.0% (10/20) in colorectal cancer with liver metastasis and 65.0% (13/20) in liver metastasis tissues. The positive expression rate of vimentin in colorectal cancer tissues was 79.0% (49/62), 85.0% (17/20) in colorectal cancer with liver metastasis and 90.0% (18/20) in liver metastasis tissues. The expression of CCR6 was closely related to lymph node metastasis (χ2=11.142, P=0.001), liver metastasis (χ2=4.694, P=0.030) and TNM stage (χ2=21.785, P 0.05). Logistic regression analysis showed that the expressions of CCR6 (OR=6.812, 95%CI: 1.206-38.474, P=0.030) and E-cadherin (OR=0.256, 95%CI: 0.069-0.945, P=0.041) were independent factors affecting the liver metastasis of colorectal cancer. Spearman correlation analysis showed that CCR6 was associated with E-cadherin expression (r=0.454, P=0.044) and vimentin expression (r=0.509, P=0.022) in 20 iver metastasis tissues of colorectal cancer. \n \n \nConclusion \nCCR6 may promote colorectal cancer progress and liver metastasis by part of epithelial-mesenchymal transition. \n \n \nKey words: \nColorectal neoplasms; Receptors, CCR6; Cadherins; Vimentin; Liver metastasis","PeriodicalId":16120,"journal":{"name":"国际肿瘤学杂志","volume":"72 1","pages":"29-34"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"国际肿瘤学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1673-422X.2020.01.005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective To detect the expressions of chemokine receptor 6 (CCR6), CC chemokine ligand 20 (CCL20) E-cadherin and vimentin in tissues of colorectal cancer and their paired liver metastases, and to investigate the possible mechanism of CCR6 in liver metastasis of colorectal cancer. Methods A total of 62 cases (54 cases of colon cancer and 8 cases of rectal cancer) of primary colorectal adenocarcinoma resection with wax lumps were selected from the First Hospital of Shanxi Medical University and Shanxi Oncology Hospital from 2009 to 2017 with complete data, including 20 samples of colorectal cancer resection with liver metastasis during the same period. The expressions of CCR6, CCL20, E-cadherin and vimentin in colorectal cancer and liver metastases tissues were detected by immunohistochemistry, and the relationships between the expressions of CCR6, E-cadherin and vimentin and the clinicopathological features of patients were analyzed. Logistic multivariate regression was used to analyze the relationship between liver metastasis and clinicopathological features, CCR6, E-cadherin and vimentin. Spearman correlation was used to analyze the correlations between CCR6 and E-cadherin and vimentin. Results The positive expression rate of CCR6 in colorectal cancer tissues was 66.1% (41/62), 85.0% (17/20) in colorectal cancer with liver metastasis and 70.0% (14/20) in liver metastasis tissues. The positive expression rate of CCL20 in colorectal cancer tissues was 83.9% (52/62), 90.0% (18/20) in colorectal cancer with liver metastasis and 90.0% (18/20) in liver metastasis tissues. The positive expression rate of E-cadherin in colorectal cancer tissues was 67.7% (42/62), 50.0% (10/20) in colorectal cancer with liver metastasis and 65.0% (13/20) in liver metastasis tissues. The positive expression rate of vimentin in colorectal cancer tissues was 79.0% (49/62), 85.0% (17/20) in colorectal cancer with liver metastasis and 90.0% (18/20) in liver metastasis tissues. The expression of CCR6 was closely related to lymph node metastasis (χ2=11.142, P=0.001), liver metastasis (χ2=4.694, P=0.030) and TNM stage (χ2=21.785, P 0.05). Logistic regression analysis showed that the expressions of CCR6 (OR=6.812, 95%CI: 1.206-38.474, P=0.030) and E-cadherin (OR=0.256, 95%CI: 0.069-0.945, P=0.041) were independent factors affecting the liver metastasis of colorectal cancer. Spearman correlation analysis showed that CCR6 was associated with E-cadherin expression (r=0.454, P=0.044) and vimentin expression (r=0.509, P=0.022) in 20 iver metastasis tissues of colorectal cancer. Conclusion CCR6 may promote colorectal cancer progress and liver metastasis by part of epithelial-mesenchymal transition. Key words: Colorectal neoplasms; Receptors, CCR6; Cadherins; Vimentin; Liver metastasis
CCR6通过上皮-间质转化促进结直肠癌肝转移
目的检测趋化因子受体6 (CCR6)、CC趋化因子配体20 (CCL20) E-cadherin和vimentin在结直肠癌及其配对肝转移组织中的表达,探讨CCR6参与结直肠癌肝转移的可能机制。方法选取2009 - 2017年山西医科大学第一医院和山西肿瘤医院资料完整的62例(结肠癌54例,直肠癌8例)原发结肠腺癌蜡块切除病例,其中同期结肠腺癌肝转移切除病例20例。采用免疫组化方法检测结直肠癌及肝转移组织中CCR6、CCL20、E-cadherin、vimentin的表达,分析CCR6、E-cadherin、vimentin的表达与患者临床病理特征的关系。采用Logistic多因素回归分析肝转移与临床病理特征、CCR6、E-cadherin、vimentin的关系。采用Spearman相关分析CCR6与E-cadherin、vimentin的相关性。结果CCR6在结直肠癌组织中的阳性表达率分别为66.1%(41/62)、85.0%(17/20)和70.0%(14/20)。CCL20在结直肠癌组织中的阳性表达率分别为83.9%(52/62)、90.0%(18/20)和90.0%(18/20)。E-cadherin在结直肠癌组织中的阳性表达率分别为67.7%(42/62)、50.0%(10/20)和65.0%(13/20)。vimentin在结直肠癌组织中的阳性表达率分别为79.0%(49/62)、85.0%(17/20)和90.0%(18/20)。CCR6的表达与淋巴结转移(χ2=11.142, P=0.001)、肝转移(χ2=4.694, P=0.030)、TNM分期(χ2=21.785, P 0.05)密切相关。Logistic回归分析显示,CCR6 (OR=6.812, 95%CI: 1.206 ~ 38.474, P=0.030)和E-cadherin (OR=0.256, 95%CI: 0.069 ~ 0.945, P=0.041)表达是影响结直肠癌肝转移的独立因素。Spearman相关分析显示,CCR6与20例结直肠癌肝转移组织中E-cadherin表达(r=0.454, P=0.044)和vimentin表达(r=0.509, P=0.022)相关。结论CCR6可能通过部分上皮-间质转化促进结直肠癌的进展和肝转移。关键词:结直肠肿瘤;受体,CCR6;钙粘蛋白;波形蛋白;肝转移
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
12123
期刊介绍:
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信