Author/Authors :
Karroum، نويسنده , , Asmae and Mirshahi، نويسنده , , Pezhman and Benabbou، نويسنده , , Nadia and Faussat، نويسنده , , Anne-Marie and Soria، نويسنده , , Jeannette and Therwath، نويسنده , , Amu and Mirshahi، نويسنده , , Massoud and Hatmi، نويسنده , , Mohamed، نويسنده ,
Abstract :
Matrix metalloproteinase-9 (MMP-9) strongly influences tumor development and metastasis. Using resistant (rMCF-7) and sensitive (sMCF-7) breast cancer lines we investigated the role of MMP-9 in cell migration (CM) and tubular network (TN) formation, two processes implied in tumor growth and metastasis. Our data demonstrate that MMP-9 which is critical for CM is necessary but not sufficient for TN formation and suggest a link between MDR1/P-gp and constitutive MMP-9. Both TN formation and CM are dependent on PKC and ERK1/2 pathways.
tudy reinforces the logic of combining therefore MMP inhibitors in cancer therapy, especially in patients with chemoresistance and invasion/metastasis.
Keywords :
MMP-9 , Breast cancer cell line MCF-7 , Cell migration , Tubular network , MDR1 phenotype , Signalling pathways