Abstract
Cell-penetrating peptides have gained attention owing to their promise in noninvasive delivery systems. Among the identified cell-penetrating peptides, the TAT peptide has been preferentially used for transduction into cells of diverse origins. However, this activity is nonselective between neoplastic and non-neoplastic cells. Here we describe artificial cell-penetrating peptides that are selectively and efficiently incorporated into human tumour cells, according to their lineage. Ten representative tumour lineage-homing cell-penetrating peptides were obtained by screening of a random peptide library constructed using messenger RNA display technology, and some of the isolates were further modified by amino-acid substitution. Their advantageous tumour cell-targeting ability is corroborated in an in vivo mouse model for imaging and growth suppression of metastatic xenoplant tumours. These cell-penetrating peptides are potentially useful for the efficient targeting of human neoplasms in a tumour origin-dependent manner, and provide a framework for the development of peptide-based anti-tumour technologies. © 2012 Macmillan Publishers Limited. All rights reserved.
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CITATION STYLE
Kondo, E., Saito, K., Tashiro, Y., Kamide, K., Uno, S., Furuya, T., … Matsushita, M. (2012). Tumour lineage-homing cell-penetrating peptides as anticancer molecular delivery systems. Nature Communications, 3. https://doi.org/10.1038/ncomms1952
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