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Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor

PURPOSE: Colorectal cancer (CRC) remains the third most common tumor worldwide. Ulcerative colitis (UC) could cause chronic inflammation and ulcers in the colon and rectum. UC is a risk factor for a high incidence of CRC, and the incidence of UC-associated CRC (UC-CRC) is still increasing. Chinese m...

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Autores principales: Yu, Cheng-Tao, Chen, Tongqing, Lu, Sicheng, Hu, Wenlong, Zhang, Qinchang, Tan, Jiani, Sun, Dongdong, Li, Liu, Sun, Xin, Xu, Changliang, Lai, Yueyang, Fan, Minmin, Shen, Zhengjie, Shen, Weixing, Cheng, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898059/
https://www.ncbi.nlm.nih.gov/pubmed/35256851
http://dx.doi.org/10.2147/JIR.S344861
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author Yu, Cheng-Tao
Chen, Tongqing
Lu, Sicheng
Hu, Wenlong
Zhang, Qinchang
Tan, Jiani
Sun, Dongdong
Li, Liu
Sun, Xin
Xu, Changliang
Lai, Yueyang
Fan, Minmin
Shen, Zhengjie
Shen, Weixing
Cheng, Haibo
author_facet Yu, Cheng-Tao
Chen, Tongqing
Lu, Sicheng
Hu, Wenlong
Zhang, Qinchang
Tan, Jiani
Sun, Dongdong
Li, Liu
Sun, Xin
Xu, Changliang
Lai, Yueyang
Fan, Minmin
Shen, Zhengjie
Shen, Weixing
Cheng, Haibo
author_sort Yu, Cheng-Tao
collection PubMed
description PURPOSE: Colorectal cancer (CRC) remains the third most common tumor worldwide. Ulcerative colitis (UC) could cause chronic inflammation and ulcers in the colon and rectum. UC is a risk factor for a high incidence of CRC, and the incidence of UC-associated CRC (UC-CRC) is still increasing. Chinese medicine prescription, Xian-Lian-Jie-Du decoction (XLJDD), has been proven its efficacy in some UC-CRC patients. However, the mechanism of XLJDD in treating UC-CRC remains unknown. This study aimed to investigate the mechanism of XLJDD in treating UC-CRC. METHODS: We constructed an AOM/DSS mouse model that could simulate the various stages of UC-CRC in humans. XLJDD and its 5 main components are used to treat the AOM/DSS model, respectively. With the power of high-throughput sequencing technology, we described the mechanism of XLJDD from transcriptomics, proteomics, and single-cell transcriptomics. RESULTS: Our results showed that XLJDD could effectively suppress the occurrence and development of colorectal tumors. Using the weighted correlation network analysis (WGCNA), several mRNA and protein modules that respond to XLJDD have been identified. Moreover, two essential genes, Mfsd2a and Ccdc85c, were caught our attention. They were prognostic markers in CRC patients, and their expression could be significantly modulated by XLJDD, showing their potential as effective targets of XLJDD. In addition, we also discovered that XLJDD could affect the cell composition of the colorectal tumor environment, especially in the infiltration of B cells. CONCLUSION: We demonstrated that XLJDD could prevent the initiation and development of colorectal tumors by modulating the expression of Mfsd2a and Ccdc85c and reducing the infiltration of B cells in the tumor microenvironment of colorectal tumor.
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spelling pubmed-88980592022-03-06 Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor Yu, Cheng-Tao Chen, Tongqing Lu, Sicheng Hu, Wenlong Zhang, Qinchang Tan, Jiani Sun, Dongdong Li, Liu Sun, Xin Xu, Changliang Lai, Yueyang Fan, Minmin Shen, Zhengjie Shen, Weixing Cheng, Haibo J Inflamm Res Original Research PURPOSE: Colorectal cancer (CRC) remains the third most common tumor worldwide. Ulcerative colitis (UC) could cause chronic inflammation and ulcers in the colon and rectum. UC is a risk factor for a high incidence of CRC, and the incidence of UC-associated CRC (UC-CRC) is still increasing. Chinese medicine prescription, Xian-Lian-Jie-Du decoction (XLJDD), has been proven its efficacy in some UC-CRC patients. However, the mechanism of XLJDD in treating UC-CRC remains unknown. This study aimed to investigate the mechanism of XLJDD in treating UC-CRC. METHODS: We constructed an AOM/DSS mouse model that could simulate the various stages of UC-CRC in humans. XLJDD and its 5 main components are used to treat the AOM/DSS model, respectively. With the power of high-throughput sequencing technology, we described the mechanism of XLJDD from transcriptomics, proteomics, and single-cell transcriptomics. RESULTS: Our results showed that XLJDD could effectively suppress the occurrence and development of colorectal tumors. Using the weighted correlation network analysis (WGCNA), several mRNA and protein modules that respond to XLJDD have been identified. Moreover, two essential genes, Mfsd2a and Ccdc85c, were caught our attention. They were prognostic markers in CRC patients, and their expression could be significantly modulated by XLJDD, showing their potential as effective targets of XLJDD. In addition, we also discovered that XLJDD could affect the cell composition of the colorectal tumor environment, especially in the infiltration of B cells. CONCLUSION: We demonstrated that XLJDD could prevent the initiation and development of colorectal tumors by modulating the expression of Mfsd2a and Ccdc85c and reducing the infiltration of B cells in the tumor microenvironment of colorectal tumor. Dove 2022-03-01 /pmc/articles/PMC8898059/ /pubmed/35256851 http://dx.doi.org/10.2147/JIR.S344861 Text en © 2022 Yu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yu, Cheng-Tao
Chen, Tongqing
Lu, Sicheng
Hu, Wenlong
Zhang, Qinchang
Tan, Jiani
Sun, Dongdong
Li, Liu
Sun, Xin
Xu, Changliang
Lai, Yueyang
Fan, Minmin
Shen, Zhengjie
Shen, Weixing
Cheng, Haibo
Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title_full Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title_fullStr Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title_full_unstemmed Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title_short Identification of Significant Modules and Targets of Xian-Lian-Jie-Du Decoction Based on the Analysis of Transcriptomics, Proteomics and Single-Cell Transcriptomics in Colorectal Tumor
title_sort identification of significant modules and targets of xian-lian-jie-du decoction based on the analysis of transcriptomics, proteomics and single-cell transcriptomics in colorectal tumor
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898059/
https://www.ncbi.nlm.nih.gov/pubmed/35256851
http://dx.doi.org/10.2147/JIR.S344861
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