Acteoside inhibits PMA‐induced matrix metalloproteinase‐9 expression <i>via</i> CaMK/ERK‐ and JNK/NF‐κB‐dependent signaling

Abstract

Acteoside inhibited PMA-induced invasion and migration of human fibrosarcoma cells via Ca(2+) -dependent CaMK/ERK and JNK/NF-κB-signaling pathways. Acteoside therefore has the potential to be a potent anticancer agent in therapeutic strategies for fibrosarcoma metastasis.

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