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Ulex Europaeus Agglutinin-I-Based Magnetic Isolation for the Efficient and Specific Capture of SW480 Circulating Colorectal Tumor Cells
[Image: see text] The efficient and specific capture of circulating tumor cells (CTCs) from patients’ peripheral blood is of significant value in precise cancer diagnosis and cancer therapy. As fine targeting molecules, lectins can recognize cancer cells specifically due to the abnormal glycosylatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435041/ https://www.ncbi.nlm.nih.gov/pubmed/36061664 http://dx.doi.org/10.1021/acsomega.2c03702 |
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author | Tian, Rongrong Li, Xiaodong Zhang, Hua Ma, Lina Zhang, Huimao Wang, Zhenxin |
author_facet | Tian, Rongrong Li, Xiaodong Zhang, Hua Ma, Lina Zhang, Huimao Wang, Zhenxin |
author_sort | Tian, Rongrong |
collection | PubMed |
description | [Image: see text] The efficient and specific capture of circulating tumor cells (CTCs) from patients’ peripheral blood is of significant value in precise cancer diagnosis and cancer therapy. As fine targeting molecules, lectins can recognize cancer cells specifically due to the abnormal glycosylation of molecules on the cancer cell membrane and the specific binding of lectin with glycoconjugates. Herein, a Ulex europaeus agglutinin-I (UEA-I)-based magnetic isolation strategy was developed to efficiently and specifically capture α-1,2-fucose overexpression CTCs from colorectal cancer (CRC) patients’ peripheral blood. Using UEA-I-modified Fe(3)O(4) magnetic beads (termed MB-UEA-I), up to 94 and 89% of target cells (i.e., SW480 CRC cells) were captured from the cell spiking complete cell culture medium and whole blood, respectively. More than 90% of captured cells show good viability and proliferation ability without detaching from MB-UEA-I. In combination with three-color immunocytochemistry (ICC) identification, MB-UEA-I has been successfully used to capture CTCs from CRC patients’ peripheral blood. The experimental results indicate a correlation between CTC characterization and tumor metastasis. Specifically, MB-UEA-I can be applied to screen early CRC by capturing CTCs when served as a liquid biopsy. The presented work offers a new insight into developing cost-effective lectin-functionalized methods for biomedical applications. |
format | Online Article Text |
id | pubmed-9435041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94350412022-09-02 Ulex Europaeus Agglutinin-I-Based Magnetic Isolation for the Efficient and Specific Capture of SW480 Circulating Colorectal Tumor Cells Tian, Rongrong Li, Xiaodong Zhang, Hua Ma, Lina Zhang, Huimao Wang, Zhenxin ACS Omega [Image: see text] The efficient and specific capture of circulating tumor cells (CTCs) from patients’ peripheral blood is of significant value in precise cancer diagnosis and cancer therapy. As fine targeting molecules, lectins can recognize cancer cells specifically due to the abnormal glycosylation of molecules on the cancer cell membrane and the specific binding of lectin with glycoconjugates. Herein, a Ulex europaeus agglutinin-I (UEA-I)-based magnetic isolation strategy was developed to efficiently and specifically capture α-1,2-fucose overexpression CTCs from colorectal cancer (CRC) patients’ peripheral blood. Using UEA-I-modified Fe(3)O(4) magnetic beads (termed MB-UEA-I), up to 94 and 89% of target cells (i.e., SW480 CRC cells) were captured from the cell spiking complete cell culture medium and whole blood, respectively. More than 90% of captured cells show good viability and proliferation ability without detaching from MB-UEA-I. In combination with three-color immunocytochemistry (ICC) identification, MB-UEA-I has been successfully used to capture CTCs from CRC patients’ peripheral blood. The experimental results indicate a correlation between CTC characterization and tumor metastasis. Specifically, MB-UEA-I can be applied to screen early CRC by capturing CTCs when served as a liquid biopsy. The presented work offers a new insight into developing cost-effective lectin-functionalized methods for biomedical applications. American Chemical Society 2022-08-17 /pmc/articles/PMC9435041/ /pubmed/36061664 http://dx.doi.org/10.1021/acsomega.2c03702 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Tian, Rongrong Li, Xiaodong Zhang, Hua Ma, Lina Zhang, Huimao Wang, Zhenxin Ulex Europaeus Agglutinin-I-Based Magnetic Isolation for the Efficient and Specific Capture of SW480 Circulating Colorectal Tumor Cells |
title | Ulex Europaeus
Agglutinin-I-Based Magnetic Isolation
for the Efficient and Specific Capture of SW480 Circulating Colorectal
Tumor Cells |
title_full | Ulex Europaeus
Agglutinin-I-Based Magnetic Isolation
for the Efficient and Specific Capture of SW480 Circulating Colorectal
Tumor Cells |
title_fullStr | Ulex Europaeus
Agglutinin-I-Based Magnetic Isolation
for the Efficient and Specific Capture of SW480 Circulating Colorectal
Tumor Cells |
title_full_unstemmed | Ulex Europaeus
Agglutinin-I-Based Magnetic Isolation
for the Efficient and Specific Capture of SW480 Circulating Colorectal
Tumor Cells |
title_short | Ulex Europaeus
Agglutinin-I-Based Magnetic Isolation
for the Efficient and Specific Capture of SW480 Circulating Colorectal
Tumor Cells |
title_sort | ulex europaeus
agglutinin-i-based magnetic isolation
for the efficient and specific capture of sw480 circulating colorectal
tumor cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435041/ https://www.ncbi.nlm.nih.gov/pubmed/36061664 http://dx.doi.org/10.1021/acsomega.2c03702 |
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