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Abstrakt

MUC1 and C-Met Affect Proliferation, Intercellular Junctions and Invasion in Two Head and Neck Carcinoma Cell Lines

Claudio Viveros-Amador, Andres Castell-Rodriguez, Edgar Zenteno, Juan Carlos Hernandez-Guerrero, Maria Dolores Jimenez-Farfan

Role of metalloproteases and adhesion molecules has been studied in cancer and metastases; tyrosine kinase receptors (TKRs) and mucins are related to their expression.

Objective: To investigate the effects of MUC1/c-Met, and their participation in metastatic mechanism in head and neck carcinoma cell lines.

Materials and methods: Lines Cal27 and A253 from squamous cell carcinoma and submaxillary gland carcinoma were treated with SU11274 (c-Met inhibitor) and GO-201 (MUC1 inhibitor) and evaluated by western blot and immunocytochemistry with anti-claudin 1, 3, and 9, integrin-αVβ1, E-cadherin, MMP2, MMP9, TIMP1 and TIMP2 after inhibition. MMPs’ activity was assessed by zymography.

Results: Claudins were atypically located in the cytoplasm and nucleus and their expression is differentially modified. Migration and invasion rate were affected by inhibition. MMP9 activity was affected.

Conclusion: Our results suggest that the role of regulating MUC1 and c-Met is related to invasion mechanisms by dysregulation of claudins and MMPs activity.