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Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer
BACKGROUND: Recurrent metastasis after radical resection in patients of colorectal cancer (CRC) is a great challenge for the world, in which genomic alterations play a major role in tumorigenesis. MUC4 plays a significant role in recurrence and metastasis in tumor. This study is aimed at exploring t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629456/ https://www.ncbi.nlm.nih.gov/pubmed/37942474 http://dx.doi.org/10.2147/IJGM.S437957 |
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author | Liu, Jieqiong Xing, Rongge Shao, Jiakang Jiao, Shunchang |
author_facet | Liu, Jieqiong Xing, Rongge Shao, Jiakang Jiao, Shunchang |
author_sort | Liu, Jieqiong |
collection | PubMed |
description | BACKGROUND: Recurrent metastasis after radical resection in patients of colorectal cancer (CRC) is a great challenge for the world, in which genomic alterations play a major role in tumorigenesis. MUC4 plays a significant role in recurrence and metastasis in tumor. This study is aimed at exploring the association between MUC4 variants and metastatic recurrence of CRC. METHODS: Forty-seven patients relapsing with metastasis and 37 patients remaining disease‐free postoperatively were enrolled. Next-generation sequencing (NGS) detected mutations. Mutation and mRNA expression data were downloaded from TCGA and cBioPortal databases. We analyzed the relationship between MUC4 variants and clinical parameters, as well as possible molecular mechanisms. RESULTS: MUC4 variants rs56359992 and rs781124621 were associated with survival in patients with CRC. Rs56359992 was more common in patients with metastatic recurrence. MAPK pathway, PI3K-Akt pathway, JAK-STAT pathway, cell cycle, WNT pathway and mTOR pathway were found to correlate with MUC4 mutation by GO/KEGG analysis, as well as resting and activated mast cell related to MUC4 mutation by CIBERSORT analysis. CONCLUSION: Genetic variants of MUC4 with CRC may constitute a molecular signature of metastatic recurrence. MUC4 may become a new target for the treatment of CRC recurrence. |
format | Online Article Text |
id | pubmed-10629456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-106294562023-11-08 Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer Liu, Jieqiong Xing, Rongge Shao, Jiakang Jiao, Shunchang Int J Gen Med Original Research BACKGROUND: Recurrent metastasis after radical resection in patients of colorectal cancer (CRC) is a great challenge for the world, in which genomic alterations play a major role in tumorigenesis. MUC4 plays a significant role in recurrence and metastasis in tumor. This study is aimed at exploring the association between MUC4 variants and metastatic recurrence of CRC. METHODS: Forty-seven patients relapsing with metastasis and 37 patients remaining disease‐free postoperatively were enrolled. Next-generation sequencing (NGS) detected mutations. Mutation and mRNA expression data were downloaded from TCGA and cBioPortal databases. We analyzed the relationship between MUC4 variants and clinical parameters, as well as possible molecular mechanisms. RESULTS: MUC4 variants rs56359992 and rs781124621 were associated with survival in patients with CRC. Rs56359992 was more common in patients with metastatic recurrence. MAPK pathway, PI3K-Akt pathway, JAK-STAT pathway, cell cycle, WNT pathway and mTOR pathway were found to correlate with MUC4 mutation by GO/KEGG analysis, as well as resting and activated mast cell related to MUC4 mutation by CIBERSORT analysis. CONCLUSION: Genetic variants of MUC4 with CRC may constitute a molecular signature of metastatic recurrence. MUC4 may become a new target for the treatment of CRC recurrence. Dove 2023-11-03 /pmc/articles/PMC10629456/ /pubmed/37942474 http://dx.doi.org/10.2147/IJGM.S437957 Text en © 2023 Liu 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 Liu, Jieqiong Xing, Rongge Shao, Jiakang Jiao, Shunchang Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title | Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title_full | Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title_fullStr | Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title_full_unstemmed | Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title_short | Relationship Between MUC4 Variants and Metastatic Recurrence in Colorectal Cancer |
title_sort | relationship between muc4 variants and metastatic recurrence in colorectal cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629456/ https://www.ncbi.nlm.nih.gov/pubmed/37942474 http://dx.doi.org/10.2147/IJGM.S437957 |
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