Identification of Tn Antigen O-GalNAc-expressing glycoproteins in human carcinomas using novel anti-Tn recombinant antibodies

Author:

Matsumoto Yasuyuki1,Kudelka Matthew R12,Hanes Melinda S1,Lehoux Sylvain1,Dutta Sucharita1,Jones Mark B1,Stackhouse Kathryn A1,Cervoni Gabrielle E1,Heimburg-Molinaro Jamie1,Smith David F2,Ju Tongzhong23,Chaikof Elliot L1,Cummings Richard D1

Affiliation:

1. Beth Israel Deaconess Medical Center, Department of Surgery, Harvard Medical School, Boston, MA

2. Emory University School of Medicine, Department of Biochemistry, Atlanta, GA

3. Current Address: Office of Biotechnology Products, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993

Abstract

Abstract The Tn antigen is a neoantigen abnormally expressed in many human carcinomas and expression correlates with metastasis and poor survival. To explore its biomarker potential, new antibodies are needed that specifically recognize this antigen in tumors. Here we generated two recombinant antibodies to the Tn antigen, Remab6 as a chimeric human IgG1 antibody and ReBaGs6 as a murine IgM antibody, and characterized their specificities using multiple biochemical and biological approaches. Both Remab6 and ReBaGs6 recognize clustered Tn structures, but most importantly do not recognize glycoforms of human IgA1 that contain potential cross-reactive Tn antigen structures. In flow cytometry and immunofluorescence analyses, Remab6 recognizes human cancer cell lines expressing the Tn antigen, but not their Tn-negative counterparts. In immunohistochemistry (IHC), Remab6 stains many human cancers in tissue array format but rarely stains normal tissues and then mostly intracellularly. We used these antibodies to identify several unique Tn containing glycoproteins in Tn-positive Colo205 cells, indicating their utility for glycoproteomics in future biomarker studies. Thus, recombinant Remab6 and ReBaGs6 are useful for biochemical characterization of cancer cells and IHC of tumors, and represent promising tools for Tn biomarker discovery independently of recognition of IgA1. [191 words].

Funder

National Institute of General Medical Sciences

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

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