The Tumor Suppressor TGFBR3 Blocks Lymph Node Metastasis in Head and Neck Cancer

• Published in: Cancers Vol. 12; no. 6; p. 1375
• Main Authors: Fang, Wei-Yu, Kuo, Yi-Zih, Chang, Jang-Yang, Hsiao, Jenn-Ren, Kao, Hung-Ying, Tsai, Sen-Tien, Wu, Li-Wha
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 27.05.2020; MDPI
• Subjects: Angiogenesis; Angiogenin; ARRB2; Arrestin; Breast cancer; Carcinogenesis; Cell adhesion & migration; Colorectal cancer; Down-regulation; Ectopic expression; Fibroblasts; Gene expression; GIPC1; Head & neck cancer; head and neck cancer; Kinases; Ligands; lymph node metastasis; Lymph nodes; Lymphatic system; Medical prognosis; Metastases; Metastasis; Motility; Oral cancer; Patients; Phosphorylation; Protein expression; Proteins; Signal transduction; Smad4 protein; Stromal cells; TGFBR3; Tumor suppressor genes; Tumorigenesis; Tumors; TGFBR3; angiogenin; ARRB2; head and neck cancer; GIPC1; lymph node metastasis
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers12061375

The TGF-β type III receptor (TGFBR3) is an essential constituent of the TGF-β signaling. In this study, we observed a down-regulation of in oral cancer, a subtype of head and neck cancer (HNC), and patients with low had poor clinical outcomes. Ectopic expression of decreased migration and invasion of oral cancer cells and lymph node metastasis of tumors, whereas depletion of had the opposite effect. In SMAD4-positive OC-2 oral cancer cells, TGFBR3-mediated suppression requires both of its cytoplasmic interacting partners ARRB2 and GIPC1. We demonstrated that TGFBR3 induces the abundance of secreted angiogenin (ANG), a known pro-angiogenic factor, and ANG is essential and sufficient to mediate TGFBR3-dependent inhibition of migration and invasion of oral cancer cells. Notably, in -deficient CAL-27 oral cancer cells, only GIPC1 is essential for -induced suppressive activity. Accordingly, HNC patients with low expressions of both and had the poorest overall survival. In summary, we conclude that TGFBR3 is as a tumor suppressor via SMAD4-dependent and -independent manner in both tumor and stromal cells during oral carcinogenesis. Our study should facilitate the possibility of using TGFBR3-mediated tumor suppression for HNC treatment.