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Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas
Head and neck squamous cell carcinoma (HNSCC) is the most common type of head and neck cancer, and has been revealed as the second-highest expression of CD44 in cancers. CD44 has been investigated as a cancer stem cell marker of HNSCC and plays a critical role in tumor malignant progression. Especia...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378409/ https://www.ncbi.nlm.nih.gov/pubmed/37504249 http://dx.doi.org/10.3390/cimb45070333 |
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author | Ishikawa, Kenichiro Suzuki, Hiroyuki Kaneko, Mika K. Kato, Yukinari |
author_facet | Ishikawa, Kenichiro Suzuki, Hiroyuki Kaneko, Mika K. Kato, Yukinari |
author_sort | Ishikawa, Kenichiro |
collection | PubMed |
description | Head and neck squamous cell carcinoma (HNSCC) is the most common type of head and neck cancer, and has been revealed as the second-highest expression of CD44 in cancers. CD44 has been investigated as a cancer stem cell marker of HNSCC and plays a critical role in tumor malignant progression. Especially, splicing variant isoforms of CD44 (CD44v) are overexpressed in cancers and considered a promising target for cancer diagnosis and therapy. We developed monoclonal antibodies (mAbs) against CD44 by immunizing mice with CD44v3–10-overexpressed PANC-1 cells. Among the established clones, C(44)Mab-18 (IgM, kappa) reacted with CHO/CD44v3–10, but not with CHO/CD44s and parental CHO-K1 using flow cytometry. The epitope mapping using peptides that cover variant exon-encoded regions revealed that C(44)Mab-18 recognized the border sequence between variant 10 and the constant exon 16-encoded sequence. These results suggest that C(44)Mab-18 recognizes variant 10-containing CD44v, but not CD44s. Furthermore, C(44)Mab-18 could recognize the human oral squamous cell carcinoma (OSCC) cell line, HSC-3, in flow cytometry. The apparent dissociation constant (K(D)) of C(44)Mab-18 for CHO/CD44v3–10 and HSC-3 was 1.6 × 10(−7) M and 1.7 × 10(−7) M, respectively. Furthermore, C(44)Mab-18 detected CD44v3–10 but not CHO/CD44s in Western blotting, and endogenous CD44v10 in immunohistochemistry using OSCC tissues. These results indicate that C(44)Mab-18 is useful for detecting CD44v10 in flow cytometry and immunohistochemistry. |
format | Online Article Text |
id | pubmed-10378409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103784092023-07-29 Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas Ishikawa, Kenichiro Suzuki, Hiroyuki Kaneko, Mika K. Kato, Yukinari Curr Issues Mol Biol Article Head and neck squamous cell carcinoma (HNSCC) is the most common type of head and neck cancer, and has been revealed as the second-highest expression of CD44 in cancers. CD44 has been investigated as a cancer stem cell marker of HNSCC and plays a critical role in tumor malignant progression. Especially, splicing variant isoforms of CD44 (CD44v) are overexpressed in cancers and considered a promising target for cancer diagnosis and therapy. We developed monoclonal antibodies (mAbs) against CD44 by immunizing mice with CD44v3–10-overexpressed PANC-1 cells. Among the established clones, C(44)Mab-18 (IgM, kappa) reacted with CHO/CD44v3–10, but not with CHO/CD44s and parental CHO-K1 using flow cytometry. The epitope mapping using peptides that cover variant exon-encoded regions revealed that C(44)Mab-18 recognized the border sequence between variant 10 and the constant exon 16-encoded sequence. These results suggest that C(44)Mab-18 recognizes variant 10-containing CD44v, but not CD44s. Furthermore, C(44)Mab-18 could recognize the human oral squamous cell carcinoma (OSCC) cell line, HSC-3, in flow cytometry. The apparent dissociation constant (K(D)) of C(44)Mab-18 for CHO/CD44v3–10 and HSC-3 was 1.6 × 10(−7) M and 1.7 × 10(−7) M, respectively. Furthermore, C(44)Mab-18 detected CD44v3–10 but not CHO/CD44s in Western blotting, and endogenous CD44v10 in immunohistochemistry using OSCC tissues. These results indicate that C(44)Mab-18 is useful for detecting CD44v10 in flow cytometry and immunohistochemistry. MDPI 2023-06-21 /pmc/articles/PMC10378409/ /pubmed/37504249 http://dx.doi.org/10.3390/cimb45070333 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ishikawa, Kenichiro Suzuki, Hiroyuki Kaneko, Mika K. Kato, Yukinari Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title | Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title_full | Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title_fullStr | Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title_full_unstemmed | Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title_short | Establishment of a Novel Anti-CD44 Variant 10 Monoclonal Antibody C(44)Mab-18 for Immunohistochemical Analysis against Oral Squamous Cell Carcinomas |
title_sort | establishment of a novel anti-cd44 variant 10 monoclonal antibody c(44)mab-18 for immunohistochemical analysis against oral squamous cell carcinomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378409/ https://www.ncbi.nlm.nih.gov/pubmed/37504249 http://dx.doi.org/10.3390/cimb45070333 |
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