Cancer Immunity, Vol. 8, p. 3 (6 February 2008) Submitted: 28 November 2007. Accepted: 7 January 2008.
Beatrice W. T. Yin1*, Ramziya Kiyamova2*, Ramon Chua1, Otavia L. Caballero1, Ivan Gout2,3, Vitalina Gryshkova2, Nimesh Bhaskaran4**, Serhiy Souchelnytskyi4**, Ulf Hellman4, Valeriy Filonenko2, Achim A. Jungbluth1, Kunle Odunsi5, Kenneth O. Lloyd6, Lloyd J. Old1 and Gerd Ritter1
1Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY, USA
2The Laboratory of Cell Growth Regulation, Department of Cell Signaling, Institute of Molecular Biology and Genetics, Kyiv, Ukraine
3Department of Biochemistry and Molecular Biology, University College London, London, United Kingdom
4Ludwig Institute for Cancer Research, BioMedical Centre, Uppsala University, Uppsala, Sweden
5Department of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, NY, USA
6Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
*These authors contributed equally to this work
**Present address: Karolinska Biomics Center, Karolinska University Hospital, SE-17176 Solna, Stockholm, Sweden
Contributed by: LJ Old
Mouse monoclonal antibody MX35 was developed against ovarian cancer. The antibody showed homogeneous reactivity with approximately 90% of human ovarian epithelial cancers and with a limited number of normal tissues by immunohistochemistry. Although mAb MX35 has been used in a number of clinical trials in ovarian cancer, it has been difficult to define the molecular identity of MX35. We report here that mAb MX35 recognizes the sodium-dependent phosphate transport protein 2b (NaPi2b) in human cancer cells. This conclusion is based on several lines of experimental evidence, including 1) the identification of SLC34A2, the gene coding for NaPi2b, by immunoscreening an ovarian cancer cell line cDNA expression library with mAb MX35; 2) mass spectrometry sequencing of peptides obtained by fragmentation from mAb MX35 affinity-purified antigen, which show complete sequence homology to amino acid sequences in NaPi2b; 3) selective down-regulation of SLC34A2 gene expression by RNA interference and the resulting loss of mAb MX35 binding to MX35-expressing human cancer cells; and 4) the demonstration of specific mAb MX35 reactivity with recombinant fusion proteins and with synthetic peptides of the putative largest extracellular loop of NaPi2b. We further show that NaPi2b in cancer cells is expressed on the cell surface as a heavily N-glycosylated protein, with evidence of additional post-translational modifications such as palmitoylation and the formation of disulfide bridges in the major extracellular loop. Membrane transporter molecules, such as NaPi2b, represent a new family of potential cell surface targets for the immunotherapy of cancer with monoclonal antibodies.
Copyright © 2008 by Gerd Ritter