to the nucleus and cytoplasm of tumor cells, respectively. Survivin depletion-triggered endogenous apoptosis and EMT inhibition, cooperating with peptide-induced mitochondrial dysfunction, enabled MIRV to markedly suppress subcutaneous tumor growth and peritoneal metastasis with minimal side effects. Taken together, the MIRV system provides an effective strategy for the simultaneous induction of apoptosis and suppression of EMT in antitumor and antimetastatic therapies.
Wang et al. (Wed,) studied this question.