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However, these glycoepitopes lack cancer specificity, and E\u2010selectin\u2010targeted glycoproteins remain largely unknown. Here, we established a framework for identifying metastasis\u2010linked glycoproteoforms. More than 70% of CRC tumors exhibited overexpression of sLeA\/X, yet without discernible associations with metastasis or survival. However, The Cancer Genome Atlas (TCGA) analysis unveiled differing expression patterns of sLeA\/X\u2010related glycogenes correlating with disease severity, indicating context\u2010dependent regulation by distinct glycosyltransferases. Deeper exploration of metastatic tumor sialoglycoproteome identified nearly 600 glycoproteins, greatly expanding our understanding of the metastasis\u2010related glycoproteome. These glycoproteins were linked to cell adhesion, oncogenic pathways, and neuroendocrine functions. Using an in\u2010house algorithm, the secretin receptor (SCTR) emerged as a top\u2010ranked targetable glycoprotein. Tumor screening confirmed SCTR's association with poor prognosis and metastasis, with N\u2010glycosylation adding cancer specificity to this glycoprotein. Prognostic links were reinforced by TCGA\u2010based investigations. In summary, SCTR, a relatively unknown CRC glycoprotein, holds potential as a biomarker of poor prognosis and as an E\u2010selectin ligand, suggesting an unforeseen role in disease dissemination. 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