Loss of adhesion/growth-regulatory galectin-9 from squamous cell epithelium in head and neck carcinomas
Language English Country Denmark Media print-electronic
Document type Journal Article
- MeSH
- Actins analysis MeSH
- Leukocyte Common Antigens analysis MeSH
- Cell Adhesion MeSH
- Cell Differentiation MeSH
- Cell Lineage MeSH
- Epithelium pathology MeSH
- Galectins analysis genetics MeSH
- Keratin-14 analysis MeSH
- Keratin-19 analysis MeSH
- Keratin-8 analysis MeSH
- Leukocytes pathology MeSH
- Humans MeSH
- Myofibroblasts pathology MeSH
- Head and Neck Neoplasms pathology MeSH
- Pharyngeal Neoplasms pathology MeSH
- Laryngeal Neoplasms pathology MeSH
- Tongue Neoplasms pathology MeSH
- Cell Proliferation MeSH
- Carcinoma, Squamous Cell pathology MeSH
- Neoplasm Staging MeSH
- Tandem Repeat Sequences genetics MeSH
- Tonsillar Neoplasms pathology MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Actins MeSH
- Leukocyte Common Antigens MeSH
- Galectins MeSH
- Keratin-14 MeSH
- Keratin-19 MeSH
- Keratin-8 MeSH
- KRT14 protein, human MeSH Browser
- KRT8 protein, human MeSH Browser
- LGALS9 protein, human MeSH Browser
- PTPRC protein, human MeSH Browser
Galectins are potent effectors of cell adhesion and growth regulation. Their expression as comples network necessitates systematic study of each member of this family. Toward this aim, we here focus on the tandem-repeat-type galectin-9. Its presence is monitored in normal squamous epithelium of the head and neck, the surgical margin, and four types of squamous cell carcinoma. Lectin presence was detected in cells of the basal layer of the epithelium. All galectin-9-negative epithelia showed aberrant positivity for keratins 14 and 19. The surgical margin presented either a normal pattern of galectin-9 and keratin presence or a mosaic-like presence/absence of galectin-9 and aberrant expression of both keratins 14 and 19. All studied specimens of squamous cell carcinoma were negative for galectin-9. When biotinylated galectin-9, or its N-terminal domain, was tested, no significant tissue reactivity for both probes was observed. Neuraminidase treatment generated reactivity to the N-domain. In conclusion, galectin-9 is expressed in the majority of samples of normal epithelium, along with regular presence of keratins 14 or 19. This lectin can represent a potential marker of normality in the cases of the studied squamous cell epithelia.
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