Abstract

Mesothelin (MSLN) is a 40-kDa cell differentiation-associated glycoprotein appearing with carcinogenesis and is highly expressed in many human cancers, including the majority of pancreatic adenocarcinomas, ovarian cancers, and mesotheliomas, while its expression in normal tissue is limited to mesothelial cells lining the pleura, pericardium, and peritoneum. Clone 11-25 is a murine hybridoma secreting monoclonal antibody (mAb) against human MSLN. In this study, we applied the 11-25 mAb to in vivo imaging to detect MSLN-expressing tumors. In in vitro and ex vivo immunochemical studies, we demonstrated specificity of 11-25 mAb to membranous MSLN expressed on several pancreatic cancer cells. We showed the accumulation of Alexa Fluor 750-labeled 11-25 mAb in MSLN-expressing tumor xenografts in athymic nude mice. Then, 11-25 mAb was labeled with 64Cu via a chelating agent DOTA and was used in both in vitro cell binding assay and in vivo positron emission tomography (PET) imaging in the tumor-bearing mice. We confirmed that 64Cu-labeled 11-25 mAb highly accumulated in MSLN-expressing tumors as compared to MSLN-negative ones. The 64Cu-labeled 11-25 mAb is potentially useful as a PET probe capable of being used for wide range of tumors, rather than 18F-FDG that occasionally provides nonspecific accumulation into the inflammatory lesions.

Highlights

  • Mesothelin (MSLN) is a 40-kDa cell differentiation-associated glycoprotein appearing with carcinogenesis

  • The protein has been named as MSLN because the expression of MSLN in normal tissue was limited to mesothelial cells lining the pleura, pericardium, and peritoneum [1]

  • The membrane-bound form of MSLN is present on a wide range of cancer cells [2,3,4,5,6,7,8,9,10,11,12,13] and its expression in normal tissues is relatively limited in the mesothelial cells

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Summary

Introduction

Mesothelin (MSLN) is a 40-kDa cell differentiation-associated glycoprotein appearing with carcinogenesis. MSLN was found as an antigen recognized by the monoclonal antibody (mAb), K1, generated by immunization of mice with the human ovarian carcinoma cell line, OVCAR-3. The protein has been named as MSLN because the expression of MSLN in normal tissue was limited to mesothelial cells lining the pleura, pericardium, and peritoneum [1]. MSLN is widely expressed in human cancers, for example, the majority of ovarian cancers and pancreatic adenocarcinomas, and in 100% of epithelial mesotheliomas. Because of its limited distribution in normal tissues and elevated expression in cancers, MSLN has the potential to become a suitable target for a wide range of cancer diagnosis and therapy by using its specific antibodies

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