Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation

被引:17
作者
Wang, Yue [1 ,2 ,3 ,4 ]
Yang, Chunxia [3 ,4 ]
Li, Wenjing [3 ,4 ]
Shen, Ying [3 ,4 ]
Deng, Jianzhong [3 ,4 ]
Lu, Wenbin [3 ,4 ]
Jin, Jianhua [3 ,4 ]
Liu, Yongping [1 ,2 ]
Liu, Qian [3 ,4 ]
机构
[1] Soochow Univ, Affiliated Hosp 3, Changzhou 213003, Jiangsu, Peoples R China
[2] Soochow Univ, Clin Oncol Lab, Changzhou Tumor Hosp, Changzhou, Peoples R China
[3] Jiangsu Univ, Dept Oncol, Wujin Hosp, Zhenjiang 213017, Jiangsu, Peoples R China
[4] Xuzhou Med Univ, Dept Oncol, Wujin Clin Coll, Xuzhou, Jiangsu, Peoples R China
来源
CANCER MEDICINE | 2021年 / 10卷 / 20期
基金
中国国家自然科学基金;
关键词
bioinformatics; colon cancer; NKD1; proliferation; WGCNA; DOWN-REGULATION; PROLIFERATION; EXPRESSION; PROMOTES;
D O I
10.1002/cam4.4224
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Colorectal cancer is an important death-related disease in the worldwide. However, specific colon cancer tumor markers currently used for diagnosis and treatment are few. The purpose of this study is to screen the potential colon cancer markers by bioinformatics and verify the results with experiments. Methods Gene expression data were downloaded from two different databases: TCGA database and GEO datasets, which were then analyzed by two different methods (difference analysis and WGCNA method). Venn and PPI analysis obtained the potential core genes, which were then performed the GO enrichment and KEGG pathway analysis. Expressions levels of NKD1 in colon carcinoma tissues were further confirmed by immunohistochemical staining and western blot assays. Moreover, the function was measured by MTT, clone formation, and tumor transplantation experiments. Importantly, co-immunoprecipitation, immunofluorescence, and protein stability assays were further performed to explore the underlying mechanism of NKD1 promoting cell proliferation. Results Nine potential core genes highly expressed in colon cancer samples were screened out by bioinformatics analysis. NKD1, one of the hub genes, highly expressed in the colon carcinoma tissues could enhance the proliferation of colon cancer cells. Mechanism research demonstrated that NKD1 was essential for the combination between Wnt signalosome (DVL) and beta-catenin, and that NKD1 knockout remarkably decreased the beta-catenin expression. Immunofluorescence assays further implied that NKD1 knockout significantly inhibited beta-catenin nuclear accumulation. Importantly, the stability of beta-catenin proteins was maintained by NKD1 in the colon cancer cells. Conclusion We believe that NKD1 well expressed in the colorectal carcinoma tissues can enhance the proliferation of colon cancer cells. Furthermore, the functions that NKD1 may have in colon cancer cells should be different from that NKD1 has played in the zebrafish. Thus, NKD1 could be a specific colorectal cancer marker.
引用
收藏
页码:7383 / 7394
页数:12
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