Development of a Novel Anti-CD44 Variant 5 Monoclonal Antibody C 44 Mab-3 for Multiple Applications against Pancreatic Carcinomas
Pancreatic cancer exhibits a poor prognosis due to the lack of early diagnostic biomarkers and the resistance to conventional chemotherapy. CD44 has been known as a cancer stem cell marker and plays tumor promotion and drug resistance roles in various cancers. In particular, the splicing variants ar...
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Published in | Antibodies (Basel) Vol. 12; no. 2 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
28.04.2023
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Subjects | |
Online Access | Get full text |
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Abstract | Pancreatic cancer exhibits a poor prognosis due to the lack of early diagnostic biomarkers and the resistance to conventional chemotherapy. CD44 has been known as a cancer stem cell marker and plays tumor promotion and drug resistance roles in various cancers. In particular, the splicing variants are overexpressed in many carcinomas and play essential roles in the cancer stemness, invasiveness or metastasis, and resistance to treatments. Therefore, the understanding of each CD44 variant's (CD44v) function and distribution in carcinomas is essential for the establishment of CD44-targeting tumor therapy. In this study, we immunized mice with CD44v3-10-overexpressed Chinese hamster ovary (CHO)-K1 cells and established various anti-CD44 monoclonal antibodies (mAbs). One of the established clones (C
Mab-3; IgG
, kappa) recognized peptides of the variant-5-encoded region, indicating that C
Mab-3 is a specific mAb for CD44v5. Moreover, C
Mab-3 reacted with CHO/CD44v3-10 cells or pancreatic cancer cell lines (PK-1 and PK-8) by flow cytometry. The apparent
of C
Mab-3 for CHO/CD44v3-10 and PK-1 was 1.3 × 10
M and 2.6 × 10
M, respectively. C
Mab-3 could detect the exogenous CD44v3-10 and endogenous CD44v5 in Western blotting and stained the formalin-fixed paraffin-embedded pancreatic cancer cells but not normal pancreatic epithelial cells in immunohistochemistry. These results indicate that C
Mab-3 is useful for detecting CD44v5 in various applications and is expected to be useful for the application of pancreatic cancer diagnosis and therapy. |
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AbstractList | Pancreatic cancer exhibits a poor prognosis due to the lack of early diagnostic biomarkers and the resistance to conventional chemotherapy. CD44 has been known as a cancer stem cell marker and plays tumor promotion and drug resistance roles in various cancers. In particular, the splicing variants are overexpressed in many carcinomas and play essential roles in the cancer stemness, invasiveness or metastasis, and resistance to treatments. Therefore, the understanding of each CD44 variant's (CD44v) function and distribution in carcinomas is essential for the establishment of CD44-targeting tumor therapy. In this study, we immunized mice with CD44v3-10-overexpressed Chinese hamster ovary (CHO)-K1 cells and established various anti-CD44 monoclonal antibodies (mAbs). One of the established clones (C
Mab-3; IgG
, kappa) recognized peptides of the variant-5-encoded region, indicating that C
Mab-3 is a specific mAb for CD44v5. Moreover, C
Mab-3 reacted with CHO/CD44v3-10 cells or pancreatic cancer cell lines (PK-1 and PK-8) by flow cytometry. The apparent
of C
Mab-3 for CHO/CD44v3-10 and PK-1 was 1.3 × 10
M and 2.6 × 10
M, respectively. C
Mab-3 could detect the exogenous CD44v3-10 and endogenous CD44v5 in Western blotting and stained the formalin-fixed paraffin-embedded pancreatic cancer cells but not normal pancreatic epithelial cells in immunohistochemistry. These results indicate that C
Mab-3 is useful for detecting CD44v5 in various applications and is expected to be useful for the application of pancreatic cancer diagnosis and therapy. |
Author | Kato, Yukinari Kaneko, Mika K Suzuki, Hiroyuki Tanaka, Tomohiro Kudo, Yuma |
Author_xml | – sequence: 1 givenname: Yuma surname: Kudo fullname: Kudo, Yuma organization: Department of Molecular Pharmacology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan – sequence: 2 givenname: Hiroyuki orcidid: 0000-0003-2646-5132 surname: Suzuki fullname: Suzuki, Hiroyuki organization: Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan – sequence: 3 givenname: Tomohiro surname: Tanaka fullname: Tanaka, Tomohiro organization: Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan – sequence: 4 givenname: Mika K orcidid: 0000-0002-4158-9208 surname: Kaneko fullname: Kaneko, Mika K organization: Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan – sequence: 5 givenname: Yukinari orcidid: 0000-0001-5385-8201 surname: Kato fullname: Kato, Yukinari organization: Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37218897$$D View this record in MEDLINE/PubMed |
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Title | Development of a Novel Anti-CD44 Variant 5 Monoclonal Antibody C 44 Mab-3 for Multiple Applications against Pancreatic Carcinomas |
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