TGF-β1 Promotes Migration and Invasion of Salivary Adenoid Cystic Carcinoma

Author:

Dong L.1,Wang Y.X.2,Li S.L.3,Yu G.Y.4,Gan Y.H.5,Li D.1,Wang C.Y.6

Affiliation:

1. Laboratory of Oral and Maxillofacial Surgery

2. Central Laboratory  Laboratory of Oral and Maxillofacial Surgery

3. Central Laboratory  Laboratory of Oral and Maxillofacial Surgery   kqshlli@bjmu.edu.cn gyyu@263.net

4. Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, 22 Zhongguancun Nandajie, Haidian District, Beijing 100081, P.R. China   kqshlli@bjmu.edu.cn gyyu@263.net

5. Central Laboratory

6. Division of Oral Biology and Medicine, UCLA School of Dentistry, Los Angeles, CA 90095, USA

Abstract

Salivary adenoid cystic carcinoma (SACC) is one of the most common subtypes of salivary gland carcinomas and frequently metastasizes to distant organs. However, little is known about the molecular mechanisms that promote SACC metastasis. In this study, we report that transforming growth factor (TGF)-β1 was highly expressed in the highly metastatic SACC-LM cell line as compared with its parental low-metastatic SACC-83 cell line. Exogenous addition of TGF-β1 induced Smad2 phosphorylation and promoted the migration and invasion of SACC-83 cells. Consistently, the inhibition of endogenous TGF-β1 signaling in SACC-LM cells by an inhibitor specific to the type I TGF-β1 receptor (TβRI) suppressed cell migration and invasion. Moreover, we found that TGF-β1 expression was significantly increased in human primary SACC samples with metastasis. Taken together, our results suggest that TGF-β1 may play a crucial role in SACC metastasis.

Publisher

SAGE Publications

Subject

General Dentistry

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