Abstract

The epidermal growth factor receptor (EGFR) is a member of the human epidermal growth factor receptor (HER) family of receptor tyrosine kinases and is involved in cell growth and differentiation. EGFR homodimers or heterodimers with other HER members, such as HER2 and HER3, activate downstream signaling cascades in many cancers. In this study, we developed novel anti-EGFR monoclonal antibodies (mAbs) and characterized their efficacy in flow cytometry, Western blot, and immunohistochemical analyses. First, we expressed the full-length or ectodomain of EGFR in LN229 glioblastoma cells and then immunized mice with LN229/EGFR or ectodomain of EGFR, and performed the first screening using enzyme-linked immunosorbent assays. Subsequently, we selected mAbs according to their efficacy in flow cytometry (second screening), Western blot (third screening), and immunohistochemical (fourth screening) analyses. Among 100 mAbs, only one clone EMab-51 (IgG1, kappa) reacted with EGFR in Western blot analysis. Finally, immunohistochemical analyses with EMab-51 showed sensitive and specific reactions against oral cancer cells, warranting the use of EMab-51 to detect EGFR in pathological analyses of EGFR-expressing cancers.

Highlights

  • The epidermal growth factor receptor (EGFR) is a transmembrane receptor that is involved in cell growth and differentiation.[1,2,3] EGFR is a member of the human epidermal growth factor receptor (HER) family of receptor tyrosine kinases

  • Of 100 monoclonal antibodies (mAbs), 94 clones reacted with A431 cells, which express endogenous EGFR.[16]. Subsequently, mAbs were further selected according to their efficacy on Western blot analysis

  • These analyses identified only one clone EMab-51 (IgG1, kappa) from EGFRec immunizations that were useful for Western blot analysis

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Summary

Introduction

The epidermal growth factor receptor (EGFR) is a transmembrane receptor that is involved in cell growth and differentiation.[1,2,3] EGFR is a member of the human epidermal growth factor receptor (HER) family of receptor tyrosine kinases. EGFR homodimers or heterodimers with other HER members, such as HER2 and HER3, activate downstream signaling cascades and control many biological processes. These pathways are frequently dysregulated via overexpression of EGFR in many cancers, including brain tumors, head and neck cancers, lung cancers, breast cancers, pancreatic cancers, kidney cancers, prostate cancers, ovary cancers, bladder cancers, and colorectal cancers.[4]. We have produced antipodoplanin (PDPN) cancer-specific mAbs (CasMabs), clone LpMab-2(8,9) and LpMab-23,(10,11) which recognize cancer-type PDPN in tumor tissues For this technology, it is critical that immunogens are produced using cancer cell lines, such as LN229 glioblastoma cells, which express cancer-specific glycan-attached membrane proteins.

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