Dysregulated expression of cell surface glycoprotein CDCP1 in prostate cancer

Lifang Yang, Sucharita M. Dutta, Dean A. Troyer, Jefferson B. Lin, Raymond A. Lance, Julius O. Nyalwidhe, Richard R. Drake, O. John Semmes

Research output: Contribution to journalArticlepeer-review

17 Scopus citations


CUB-domain-containing protein 1 (CDCP1) is a trans-membrane protein regulator of cell adhesion with a potent pro-migratory function in tumors. Given that proteolytic cleavage of the ectodomain correlates with outside-in oncogenic signaling, we characterized glycosylation in the context of cellular processing and expression of CDCP1 in prostate cancer. We detected 135 kDa full-length and proteolytic processed 70 kDa species in a panel of PCa cell models. The relative expression of full-length CDCP1 correlated with the metastatic potential of syngeneic cell models and an increase in surface membrane expression of CDCP1 was observed in tumor compared to adjacent normal prostate tissues. We demonstrated that glycosylation of CDCP1 is a prerequisite for protein stability and plasma membrane localization, and that the expression level and extent of N-glycosylation of CDCP1 correlated with metastatic status. Interestingly, complex N-linked glycans with sialic acid chains were restricted to the N-terminal half of the ectodomain and absent in the truncated species. Characterization of the extracellular expression of CDCP1 identified novel circulating forms and revealed that extracellular vesicles provide additional processing pathways. Employing immunoaffinity mass spectrometry, we detected elevated levels of circulating CDCP1 in patient urine with high-risk disease. Our results establish that differential glycosylation, cell surface presentation and extracellular expression of CDCP1 are hallmarks of PCa progression.

Original languageEnglish (US)
Pages (from-to)43743-43758
Number of pages16
Issue number41
StatePublished - 2015
Externally publishedYes


  • Biomarker
  • CUB-domain containing protein 1
  • Glycoprotein
  • Prostate cancer

ASJC Scopus subject areas

  • Oncology


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