Comparative analysis of alpha2,3/2,6-linked N-acetylneuraminic acid and cytokeratin expression in head and neck squamous cell carcinoma
- PMID: 15254692
Comparative analysis of alpha2,3/2,6-linked N-acetylneuraminic acid and cytokeratin expression in head and neck squamous cell carcinoma
Abstract
Head and neck squamous cell cancer (HNSCC) requires precise characterization of their biological properties to better stratify treatment approaches. Some biological features of tumor cells are related to altered glycosylation of their surface. This study characterized alpha2,3/6-N-acetylneuraminic acid (NeuNAc) expression in adult squamous epithelia of primary and metastatic HNSCC in relation to expression of well established differentiation markers, such as cytokeratins. The expression of NeuNAc was assessed by plant lectins: Maackia amurensis agglutinin type 2 (MAA) and Sambucus nigra agglutinin (SNA) specific for alpha2,3NeuNAc and alpha2,6NeuNAc, respectively. Double labeling studies at the single-cell level were performed to compare alpha2,3/6NeuNAc linkage with expression of intermediate filaments. In studied normal adult epithelia, predominantly basal expression of alpha2,6NeuNAc and suprabasal expression of alpha2,3NeuNAc was seen, showing their differentiation-dependent linkage. The cells with markers of terminal differentiation (i.e. CK10+ alpha2,3NeuNAc+ alpha2,6NeuNAc-) prevailed in HNSCC, with increasing proportion from differentiation grade G1 to G3. High proportions of cytokeratin pCK37+ carcinoma cells occurred in all studied tumors and were accompanied by a hypersialylated phenotype (i.e. alpha2,3 NeuNAc+ alpha2,6NeuNAc+) not generally seen in non-transformed epithelia. It is hypothesized that these cells could be the pool for tumor spreading in the organism. Monitoring HNSCC using multiparameter phenotype analysis can produce new data important for the understanding of the biological behavior of HNSCC, and useful for the treatment rationalization.
Similar articles
-
Correlation of expression of nuclear proteins pKi67 and p63 with lectin histochemical features in head and neck squamous cell cancer.Int J Oncol. 2005 Aug;27(2):409-15. Int J Oncol. 2005. PMID: 16010422
-
Expression of galectin-3-reactive ligands in squamous cancer and normal epithelial cells as a marker of differentiation.Int J Oncol. 2001 Jul;19(1):59-64. Int J Oncol. 2001. PMID: 11408923
-
Cytokeratins 6 and 16 are frequently expressed in head and neck squamous cell carcinoma cell lines and fresh biopsies.Anticancer Res. 2005 Jul-Aug;25(4):2675-80. Anticancer Res. 2005. PMID: 16080511
-
Glycobiology of head and neck squamous epithelia and carcinomas.ORL J Otorhinolaryngol Relat Spec. 2005;67(2):61-9. doi: 10.1159/000084994. Epub 2005 Apr 8. ORL J Otorhinolaryngol Relat Spec. 2005. PMID: 15821350 Review.
-
Cancer stem cells in head and neck squamous cell cancer.J Clin Oncol. 2008 Jun 10;26(17):2871-5. doi: 10.1200/JCO.2007.15.1613. J Clin Oncol. 2008. PMID: 18539966 Review.
Cited by
-
LC-MS/MS of isomeric N-and O-glycopeptides on mesoporous graphitized carbon column.Anal Chim Acta. 2024 Aug 15;1317:342907. doi: 10.1016/j.aca.2024.342907. Epub 2024 Jun 25. Anal Chim Acta. 2024. PMID: 39030008 Free PMC article.
-
Isomeric Separation of N-Glycopeptides Derived from Glycoproteins by Porous Graphitic Carbon (PGC) LC-MS/MS.Anal Chem. 2020 Jul 21;92(14):9556-9565. doi: 10.1021/acs.analchem.0c00668. Epub 2020 Jul 6. Anal Chem. 2020. PMID: 32544320 Free PMC article.
-
LC-MS/MS isomeric profiling of permethylated N-glycans derived from serum haptoglobin of hepatocellular carcinoma (HCC) and cirrhotic patients.Electrophoresis. 2017 Sep;38(17):2160-2167. doi: 10.1002/elps.201700025. Epub 2017 Jul 14. Electrophoresis. 2017. PMID: 28543513 Free PMC article.
-
Plant lectin can target receptors containing sialic acid, exemplified by podoplanin, to inhibit transformed cell growth and migration.PLoS One. 2012;7(7):e41845. doi: 10.1371/journal.pone.0041845. Epub 2012 Jul 23. PLoS One. 2012. PMID: 22844530 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials