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Exploring the potential of mucin 13 (MUC13) as a biomarker for carcinomas and other diseases

  • Panagiota S. Filippou , Annie H. Ren , Dimitrios Korbakis , Lampros Dimitrakopoulos , Antoninus Soosaipillai , Vivian Barak , Shahar Frenkel , Jacob Pe’er , Michal Lotem , Sharon Merims , Rafael Molina , Ivan Blasutig ORCID logo , Dimitrios P. Bogdanos and Eleftherios P. Diamandis EMAIL logo
Published/Copyright: May 16, 2018

Abstract

Background:

Mucin 13 (MUC13) is a cell surface glycoprotein aberrantly expressed in a variety of epithelial carcinomas. Thus far, the role of MUC13 in various diseases remains elusive. To the best of our knowledge, this is the first study to examine the potential of MUC13 as a serum biomarker in a variety of carcinomas and other conditions.

Methods:

We developed a recombinant MUC13 protein, mouse monoclonal antibodies and enzyme immunoassay (ELISA) for MUC13. We used this assay to measure MUC13 levels in the supernatants of cancer cell lines and a large cohort of serum samples from healthy and diseased individuals.

Results:

MUC13 is secreted from cancer cell lines, with highest levels found in ovarian cancer cell lines. MUC13 levels in human sera were significantly increased in patients with renal failure and 20%–30% of patients with ovarian, liver, lung and other cancers. MUC13 was also elevated in 70% of patients with active cutaneous melanoma, but not uveal melanoma. Furthermore, we identified significant MUC13 elevations in the serum of patients with vasculitis (ANCA-positive) autoantibodies, but not in those with inflammatory bowel disease.

Conclusions:

Serum MUC13 is frequently elevated not only in a variety of malignant cases but also in some benign pathologies, thus appearing to be a non-specific disease biomarker. Nonetheless, serum MUC13 is clearly highly elevated in some carcinoma patients, and its relationship with tumor progression in this context warrant further research. Future studies that examine the correlation between serum MUC13 levels to stage of cancer could elucidate prognostic potential.


Corresponding author: Eleftherios P. Diamandis, PhD, MD, Mount Sinai Hospital, Joseph and Wolf Lebovic Ctr., 60 Murray St [Box 32], Flr 6 – Rm L6-201, Toronto, ON, M5T 3L9, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada; Department of Clinical Biochemistry, University Health Network, Toronto, ON, Canada; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada; and Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, Canada, Phone: +416-586-8443, Fax: +416-619-5521

Acknowledgments

We thank Dr. Davor Brinc for fruitful discussions and for determining the analytical parameters of the MUC13 ELISA.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This study was funded by the principal investigator’s research fund from Mount Sinai Hospital.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2018-02-06
Accepted: 2018-04-10
Published Online: 2018-05-16
Published in Print: 2018-10-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

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