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Kallistatin induces breast cancer cell apoptosis and autophagy by modulating Wnt signaling and microRNA synthesis
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Kallistatin reduces viability and increases apoptosis in breast cancer cells.

Kallistatin induces autophagy via suppressing Wnt signaling.

Kallistatin via its active site regulates miR-21, miR-203 and miR-34a synthesis.

Kallistatin inhibits miR-203 and increases SOCS3 levels via PKC-ERK signaling.

Novel mechanisms of kallistatin in cancer cell death and tumor development.

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