The expression of keratan sulfate in malignant melanoma enhances the adhesion and invasion activity of melanoma cells.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Oct 2022
Historique:
revised: 29 05 2022
received: 03 01 2022
accepted: 13 06 2022
pubmed: 12 7 2022
medline: 12 10 2022
entrez: 11 7 2022
Statut: ppublish

Résumé

Mammals express a wide variety of glycans that include N-glycans, O-glycans, proteoglycans, glycolipids, etc. Glycan expression can modulate the cellular functions, and hence is strongly involved in the onset and progression of numerous diseases. Here, we report the relevance of the ectopic expression of keratan sulfate (KS) glycan chains in human malignant melanomas. Using a human melanoma cell line, we found that the KS enhanced the invasiveness of the cells but caused no change in the growth rate of the cells. The phosphorylation of paxillin, a focal adhesion-associated adaptor protein, was strong at the region where KS was expressed in the melanoma tissues, indicating that KS stimulated the phosphorylation of paxillin. We also observed that KS enhanced the adhesion of melanoma cells and this was accompanied by a greatly increased level of phosphorylation of paxillin. These data suggest that the expression of KS contributes to the development of malignant phenotypes such as strong cell adhesion and the invasiveness of melanoma cells.

Identifiants

pubmed: 35811379
doi: 10.1111/1346-8138.16506
doi:

Substances chimiques

Glycolipids 0
Paxillin 0
Proteoglycans 0
Keratan Sulfate 9056-36-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1027-1036

Subventions

Organisme : An original foundation to facilitate intra-center collaboration at Osaka International Cancer Institute
Organisme : Grants-in-Aid for Scientific Research C
ID : 20K07629
Organisme : Takeda Science Foundation

Informations de copyright

© 2022 Japanese Dermatological Association.

Références

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Auteurs

Kota Tachibana (K)

Department of Dermatologic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Department of Dermatology, Dentistry and Pharmaceutical Science, Okayama University Graduate School of Medicine, Okayama, Japan.

Yuki Ohkawa (Y)

Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

Noriko Kanto (N)

Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

Kento Maeda (K)

Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

Shuichi Ohe (S)

Department of Dermatologic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Taiki Isei (T)

Department of Dermatologic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Yoichiro Harada (Y)

Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

Naoyuki Taniguchi (N)

Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, Osaka, Japan.

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