TGFβ1-Smad3-Jagged1-Notch1-Slug signaling pathway takes part in tumorigenesis and progress of tongue squamous cell carcinoma.

BACKGROUND: TGF beta 1 and Smad3 play an important role in the process of EMT. TGF beta 1 regulates the expression of Jagged1 by modulating Notch signaling. Jagged1 is related to tumor invasion, metastasis, chemotherapy resistance, and tumor immune escape. The aims of this study are to examine deregulation of TGF beta 1-Smad3-Jagged1-Notch1-Slug signaling in TSCC and to investigate its roles in TSCC progression. MATERIALS AND METHODS: Notch1, Smad3, Jagged1 and Slug proteins and mRNA expression were detected in specimens from 89 cases of patients. We analyzed the correlation between their expressions and histological grade, clinical stage and lymph node metastasis. RESULTS: Notch1, Smad3, Jagged1 and Slug mRNA expressions in TSCC were higher than normal tissue (P < 0.05). The protein expression of Notch1 and Smad3 in TSCC were higher (chi(2) = 7.30, P < 0.01 and chi(2) = 5.84, P < 0.05). Notch1 and Smad3 expressions were correlated with clinical stage (chi(2) = 18.81, P < 0.01; chi(2) = 22.29, P < 0.01), but not Jagged1 (chi(2) = 0.53, P > 0.05). The Slug protein expression was correlated with clinical stage. The positive rate of Notch1 was higher in lymph node metastases positive cases (chi(2) = 7.30, P < 0.01). Moreover, higher expression of Jagged1 was found in lymph node positive cases (chi(2) = 10.82, P < 0.01). CONCLUSIONS: The key protein expression in TGF beta 1-Smad3-Jagged1-Notch1-Slug signaling pathway significantly correlated with the clinicopathological features of TSCC patients. It's potential as a biomarker and a novel therapeutic target for TSCC patients at risk of metastasis. It may play an irreplaceable role in TSCC progression which may attribute to promoting EMT which enhances cell migration, invasion and metastasis.