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This study was performed to evaluate the likely of the CPPs with tumor-targeting Houses to provide a cytotoxic payload to HCC cells. We explored using a CXCR4-targeting peptide, T22, fused with cytotoxic peptide PE24, as a novel therapeutic approach for CXCR4+ HCC cells. T22 was preferred since the nanocarrier because of its nicely-proven purpose a

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