Tspan15 plays a crucial role in metastasis in oral squamous cell carcinoma.


Journal

Experimental cell research
ISSN: 1090-2422
Titre abrégé: Exp Cell Res
Pays: United States
ID NLM: 0373226

Informations de publication

Date de publication:
15 11 2019
Historique:
received: 02 12 2018
revised: 01 09 2019
accepted: 09 09 2019
pubmed: 14 9 2019
medline: 17 6 2020
entrez: 14 9 2019
Statut: ppublish

Résumé

Tetraspanin 15 (Tspan15) is a member of the tetraspanin family, which is associated with various biological events and several diseases, however, its role in human oral squamous cell carcinoma (OSCC) remains unknown. The current study aimed to clarify the role of Tspan15 in OSCC. The mRNA and protein expression levels of Tspan15 were up-regulated in OSCC cases and OSCC-derived cell lines. Significant up-regulated Tspan15 expression was found in the advanced OSCC cases; primary tumoral size (P = 0.042), regional lymph node metastasis (P = 0.036) and TNM classification (P = 0.024). The decreased expression of Tspan15 did not significantly affect cellular proliferation, whereas tumoral invasion and migration activities were suppressed in Tspan15-down-regulated cells, suggesting that Tspan15 might activate metastasis-related signaling. Moreover, in the Tspan15-down-regulated cells, the expression of a disintegrin and metalloproteinase (ADAM) 10 was also down-regulated and the cells secreted less soluble N-cadherin compared with control cells. And weak immunoreactivity of β-catenin in the nucleus was detected in Tspan15-down-regulated cells compared with the control cells. These findings suggested that overexpression of Tspan15 positively regulates development of OSCC, and that ADAM10, N-cadherin, β-catenin might be involved in the Tspan15-mediated pathway. These unusual conditions of cell adhesion molecules may lead to high metastasis rate found in Tspan15-overexpressing cases.

Identifiants

pubmed: 31518558
pii: S0014-4827(19)30484-7
doi: 10.1016/j.yexcr.2019.111622
pii:
doi:

Substances chimiques

Cadherins 0
Cell Adhesion Molecules 0
TSPAN15 protein, human 0
Tetraspanins 0
beta Catenin 0
ADAM10 Protein EC 3.4.24.81

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111622

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Kazuya Hiroshima (K)

Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.

Masashi Shiiba (M)

Department of Medical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan; Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan. Electronic address: m.shiiba@faculty.chiba-u.jp.

Noritoshi Oka (N)

Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.

Fumihiko Hayashi (F)

Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.

Sho Ishida (S)

Department of Dentistry and Oral Surgery, Chiba Medical Center, Chiba, Japan.

Reo Fukushima (R)

Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

Kazuyuki Koike (K)

Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

Manabu Iyoda (M)

Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

Dai Nakashima (D)

Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

Hideki Tanzawa (H)

Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan; Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

Katsuhiro Uzawa (K)

Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan; Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.

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Classifications MeSH