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Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers

BACKGROUND: Circulating tumor cells (CTCs) in peripheral blood have been shown to reflect the prognosis of patients with colorectal cancer, and epithelial and mesenchymal markers further predict the likelihood of cancer dissemination. This study was conducted to identify possible association of clin...

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Autores principales: Xing, Yasi, Qin, Fangyuan, Zhai, Yaping, Yang, Jingwen, Yan, Yiyang, Li, Dan, Zhang, Han, Hu, Renwang, Xu, Xianjing, Cao, Xuanchao, Huang, Gairong, Liu, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050256/
https://www.ncbi.nlm.nih.gov/pubmed/35493298
http://dx.doi.org/10.1155/2022/5105599
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author Xing, Yasi
Qin, Fangyuan
Zhai, Yaping
Yang, Jingwen
Yan, Yiyang
Li, Dan
Zhang, Han
Hu, Renwang
Xu, Xianjing
Cao, Xuanchao
Huang, Gairong
Liu, Xiang
author_facet Xing, Yasi
Qin, Fangyuan
Zhai, Yaping
Yang, Jingwen
Yan, Yiyang
Li, Dan
Zhang, Han
Hu, Renwang
Xu, Xianjing
Cao, Xuanchao
Huang, Gairong
Liu, Xiang
author_sort Xing, Yasi
collection PubMed
description BACKGROUND: Circulating tumor cells (CTCs) in peripheral blood have been shown to reflect the prognosis of patients with colorectal cancer, and epithelial and mesenchymal markers further predict the likelihood of cancer dissemination. This study was conducted to identify possible association of clinical features of colorectal cancer with CTC counts, their subtypes, and systemic inflammatory markers. METHODS: Blood samples of 316 colorectal cancer patients were used for CTC detection and subtyping with EpCAM, CK8/18/19, vimentin, and twist as biomarkers. The neutrophil/lymphocyte ratio, platelet/lymphocyte ratio, C-reactive protein/albumin ratio, lymphocyte/monocyte ratio, and systemic immune-inflammation index (SII) were also measured. The relationship between clinical data and these markers or parameters was analyzed. RESULTS: Total CTC counts were correlated with whether there was lymph node involvement but was not correlated with TNM staging. There was a difference in mesenchymal CTCs between patients with and without lymph node involvement (P < 0.05). Also, more patients with metastasis tested positive for mesenchymal CTCs (P < 0.05). Of the systemic inflammatory markers, platelet/lymphocyte ratio was positively correlated with CTC counts (P < 0.01), and lymphocyte/monocyte ratio was negatively correlated with CTC counts (P < 0.05). CONCLUSIONS: Colorectal cancer patients with the mesenchymal markers on their CTCs are more likely to have lymph node involvement or distant metastasis than those without these markers.
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spelling pubmed-90502562022-04-29 Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers Xing, Yasi Qin, Fangyuan Zhai, Yaping Yang, Jingwen Yan, Yiyang Li, Dan Zhang, Han Hu, Renwang Xu, Xianjing Cao, Xuanchao Huang, Gairong Liu, Xiang Dis Markers Research Article BACKGROUND: Circulating tumor cells (CTCs) in peripheral blood have been shown to reflect the prognosis of patients with colorectal cancer, and epithelial and mesenchymal markers further predict the likelihood of cancer dissemination. This study was conducted to identify possible association of clinical features of colorectal cancer with CTC counts, their subtypes, and systemic inflammatory markers. METHODS: Blood samples of 316 colorectal cancer patients were used for CTC detection and subtyping with EpCAM, CK8/18/19, vimentin, and twist as biomarkers. The neutrophil/lymphocyte ratio, platelet/lymphocyte ratio, C-reactive protein/albumin ratio, lymphocyte/monocyte ratio, and systemic immune-inflammation index (SII) were also measured. The relationship between clinical data and these markers or parameters was analyzed. RESULTS: Total CTC counts were correlated with whether there was lymph node involvement but was not correlated with TNM staging. There was a difference in mesenchymal CTCs between patients with and without lymph node involvement (P < 0.05). Also, more patients with metastasis tested positive for mesenchymal CTCs (P < 0.05). Of the systemic inflammatory markers, platelet/lymphocyte ratio was positively correlated with CTC counts (P < 0.01), and lymphocyte/monocyte ratio was negatively correlated with CTC counts (P < 0.05). CONCLUSIONS: Colorectal cancer patients with the mesenchymal markers on their CTCs are more likely to have lymph node involvement or distant metastasis than those without these markers. Hindawi 2022-04-21 /pmc/articles/PMC9050256/ /pubmed/35493298 http://dx.doi.org/10.1155/2022/5105599 Text en Copyright © 2022 Yasi Xing et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xing, Yasi
Qin, Fangyuan
Zhai, Yaping
Yang, Jingwen
Yan, Yiyang
Li, Dan
Zhang, Han
Hu, Renwang
Xu, Xianjing
Cao, Xuanchao
Huang, Gairong
Liu, Xiang
Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title_full Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title_fullStr Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title_full_unstemmed Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title_short Association of Clinical Features of Colorectal Cancer with Circulating Tumor Cells and Systemic Inflammatory Markers
title_sort association of clinical features of colorectal cancer with circulating tumor cells and systemic inflammatory markers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050256/
https://www.ncbi.nlm.nih.gov/pubmed/35493298
http://dx.doi.org/10.1155/2022/5105599
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