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

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 wi...

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Autores principales: Wang, Yue, Yang, Chunxia, Li, Wenjing, Shen, Ying, Deng, Jianzhong, Lu, Wenbin, Jin, Jianhua, Liu, Yongping, Liu, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525156/
https://www.ncbi.nlm.nih.gov/pubmed/34547189
http://dx.doi.org/10.1002/cam4.4224
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author Wang, Yue
Yang, Chunxia
Li, Wenjing
Shen, Ying
Deng, Jianzhong
Lu, Wenbin
Jin, Jianhua
Liu, Yongping
Liu, Qian
author_facet Wang, Yue
Yang, Chunxia
Li, Wenjing
Shen, Ying
Deng, Jianzhong
Lu, Wenbin
Jin, Jianhua
Liu, Yongping
Liu, Qian
author_sort Wang, Yue
collection PubMed
description 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 β‐catenin, and that NKD1 knockout remarkably decreased the β‐catenin expression. Immunofluorescence assays further implied that NKD1 knockout significantly inhibited β‐catenin nuclear accumulation. Importantly, the stability of β‐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.
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spelling pubmed-85251562021-10-26 Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation Wang, Yue Yang, Chunxia Li, Wenjing Shen, Ying Deng, Jianzhong Lu, Wenbin Jin, Jianhua Liu, Yongping Liu, Qian Cancer Med Bioinformatics 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 β‐catenin, and that NKD1 knockout remarkably decreased the β‐catenin expression. Immunofluorescence assays further implied that NKD1 knockout significantly inhibited β‐catenin nuclear accumulation. Importantly, the stability of β‐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. John Wiley and Sons Inc. 2021-09-21 /pmc/articles/PMC8525156/ /pubmed/34547189 http://dx.doi.org/10.1002/cam4.4224 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Bioinformatics
Wang, Yue
Yang, Chunxia
Li, Wenjing
Shen, Ying
Deng, Jianzhong
Lu, Wenbin
Jin, Jianhua
Liu, Yongping
Liu, Qian
Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title_full Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title_fullStr Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title_full_unstemmed Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title_short Identification of colon tumor marker NKD1 via integrated bioinformatics analysis and experimental validation
title_sort identification of colon tumor marker nkd1 via integrated bioinformatics analysis and experimental validation
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525156/
https://www.ncbi.nlm.nih.gov/pubmed/34547189
http://dx.doi.org/10.1002/cam4.4224
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