Development of a Novel Anti-CD44 Variant 8 Monoclonal Antibody C 44 Mab-94 against Gastric Carcinomas.
Hiroyuki SuzukiNohara GotoTomohiro TanakaTsunenori OuchidaMika K KanekoYukinari KatoPublished in: Antibodies (Basel, Switzerland) (2023)
Gastric cancer (GC) is the third leading cause of cancer-related deaths worldwide. GC with peritoneal metastasis exhibits a poor prognosis due to the lack of effective therapy. A comprehensive analysis of malignant ascites identified the genomic alterations and significant amplifications of cancer driver genes, including CD44 . CD44 and its splicing variants are overexpressed in tumors, and play crucial roles in the acquisition of invasiveness, stemness, and resistance to treatments. Therefore, the development of CD44-targeted monoclonal antibodies (mAbs) is important for GC diagnosis and therapy. In this study, we immunized mice with CD44v3-10-overexpressed PANC-1 cells and established several dozens of clones that produce anti-CD44v3-10 mAbs. One of the clones (C 44 Mab-94; IgG 1 , kappa) recognized the variant-8-encoded region and peptide, indicating that C 44 Mab-94 is a specific mAb for CD44v8. Furthermore, C 44 Mab-94 could recognize CHO/CD44v3-10 cells, oral squamous cell carcinoma cell line (HSC-3), or GC cell lines (MKN45 and NUGC-4) in flow cytometric analyses. C 44 Mab-94 could detect the exogenous CD44v3-10 and endogenous CD44v8 in western blotting and stained the formalin-fixed paraffin-embedded gastric cancer cells. These results indicate that C 44 Mab-94 is useful for detecting CD44v8 in a variety of experimental methods and is expected to become usefully applied to GC diagnosis and therapy.
Keyphrases
- monoclonal antibody
- poor prognosis
- nk cells
- stem cells
- long non coding rna
- epithelial mesenchymal transition
- squamous cell carcinoma
- metabolic syndrome
- mesenchymal stem cells
- drug delivery
- immune response
- transcription factor
- cell proliferation
- cell cycle arrest
- toll like receptor
- mass spectrometry
- papillary thyroid
- high grade