Translational study reveals preferential keratan sulfate expression in papillary thyroid carcinoma, highlighting utility for distinguishing metastases from benign inclusions.
Keratan sulfate (KS) is a glycosaminoglycan consisting of repeating N -acetyllactosamine disaccharides, in which both galactose and N -acetylglucosamine are often 6- O -sulfated. It has been reported that KS recognized by the monoclonal antibodies 5D4 and 373E1 is preferentially expressed in papillary thyroid carcinoma (PTC) and only minimally in other thyroid tumors/lesions or normal thyroid tissue. However, the precise epitopes recognized by these antibodies remain incompletely characterized, and the expression and extent of low-sulfated KS in PTC have not been systematically evaluated. To better understand the nature of KS expressed in PTC, we generated a novel anti-KS monoclonal antibody, 299-1C1, and performed immunohistochemical analyses using 299-1C1 together with two existing anti-KS monoclonal antibodies, 5D4 and R-10G, in combination with keratanase II and endo-β-galactosidase. The results showed that both highly sulfated and low-sulfated KS are preferentially expressed in PTC, including lymph node metastases, accompanied by upregulation of genes encoding key KS biosynthetic enzymes ( B3GNT7 , B4GALT4 , CHST2 , and CHST6 ) in integrated TCGA/GTEx transcriptomic datasets. Expression of B3GNT7 , B4GALT4 , and CHST2 , but not CHST6 , was further increased in BRAF -mutant PTCs. These findings indicate that anti-KS monoclonal antibodies are useful for the pathological diagnosis of PTC, particularly for distinguishing lymph node metastases from intranodal thyroid inclusions.
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Kato et al. (2026) studied this question.
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