Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage
Nian-Qiu Shi, Wei Gao, Bai Xiang, Xian-Rong QiDepartment of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing, People's Republic of ChinaAbstract: The use of activable cell-penetrating peptides (ACPPs) as molecular imaging probes is a promising new approach for...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2012-03-01
|
Series: | International Journal of Nanomedicine |
Online Access: | http://www.dovepress.com/enhancing-cellular-uptake-of-activable-cell-penetrating-peptidendashdo-a9565 |
id |
doaj-7c57eeedc2ef4f7681015add8c9a36f9 |
---|---|
record_format |
Article |
spelling |
doaj-7c57eeedc2ef4f7681015add8c9a36f92020-11-24T22:48:54ZengDove Medical PressInternational Journal of Nanomedicine1176-91141178-20132012-03-012012default16131621Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavageShi NQGao WXiang BQi XRNian-Qiu Shi, Wei Gao, Bai Xiang, Xian-Rong QiDepartment of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing, People's Republic of ChinaAbstract: The use of activable cell-penetrating peptides (ACPPs) as molecular imaging probes is a promising new approach for the visualization of enzymes. The cell-penetrating function of a polycationic cell-penetrating peptide (CPP) is efficiently blocked by intramolecular electrostatic interactions with a polyanionic peptide. Proteolysis of a proteinase-sensitive substrate present between the CPP and polyanionic peptide affords dissociation of both domains and enables the activated CPP to enter cells. This ACPP strategy could also be used to modify antitumor agents for tumor-targeting therapy. Here, we aimed to develop a conjugate of ACPP with antitumor drug doxorubicin (DOX) sensitive to matrix metalloproteinase-2 and -9 (MMP-2/9) for tumor-targeting therapy purposes. The ACPP-DOX conjugate was successfully synthesized. Enzymatic cleavage of ACPP-DOX conjugate by matrix metalloproteinase (MMP)-2/9 indicated that the activation of ACPP-DOX occurred in an enzyme concentration–dependent manner. Flow cytometry and laser confocal microscope studies revealed that the cellular uptake of ACPP-DOX was enhanced after enzymatic-triggered activation and was higher in HT-1080 cells (overexpressed MMPs) than in MCF-7 cells (under-expressed MMPs). The antiproliferative assay showed that ACPP had little toxicity and that ACPP-DOX effectively inhibited HT-1080 cell proliferation. These experiments revealed that the ACPP-DOX conjugate could be triggered by MMP-2/9, which enabled the activated CPP-DOX to enter cells. ACPP-DOX conjugate may be a potential prodrug delivery system used to carry antitumor drugs for MMP-related tumor therapy.Keywords: activable cell-penetrating peptide, matrix metalloproteinase, proteinase-sensitive substrate, cellular uptake, antiproliferative, enzymatic cleavage, tumor extracellular environmenthttp://www.dovepress.com/enhancing-cellular-uptake-of-activable-cell-penetrating-peptidendashdo-a9565 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shi NQ Gao W Xiang B Qi XR |
spellingShingle |
Shi NQ Gao W Xiang B Qi XR Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage International Journal of Nanomedicine |
author_facet |
Shi NQ Gao W Xiang B Qi XR |
author_sort |
Shi NQ |
title |
Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
title_short |
Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
title_full |
Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
title_fullStr |
Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
title_full_unstemmed |
Enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
title_sort |
enhancing cellular uptake of activable cell-penetrating peptide–doxorubicin conjugate by enzymatic cleavage |
publisher |
Dove Medical Press |
series |
International Journal of Nanomedicine |
issn |
1176-9114 1178-2013 |
publishDate |
2012-03-01 |
description |
Nian-Qiu Shi, Wei Gao, Bai Xiang, Xian-Rong QiDepartment of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing, People's Republic of ChinaAbstract: The use of activable cell-penetrating peptides (ACPPs) as molecular imaging probes is a promising new approach for the visualization of enzymes. The cell-penetrating function of a polycationic cell-penetrating peptide (CPP) is efficiently blocked by intramolecular electrostatic interactions with a polyanionic peptide. Proteolysis of a proteinase-sensitive substrate present between the CPP and polyanionic peptide affords dissociation of both domains and enables the activated CPP to enter cells. This ACPP strategy could also be used to modify antitumor agents for tumor-targeting therapy. Here, we aimed to develop a conjugate of ACPP with antitumor drug doxorubicin (DOX) sensitive to matrix metalloproteinase-2 and -9 (MMP-2/9) for tumor-targeting therapy purposes. The ACPP-DOX conjugate was successfully synthesized. Enzymatic cleavage of ACPP-DOX conjugate by matrix metalloproteinase (MMP)-2/9 indicated that the activation of ACPP-DOX occurred in an enzyme concentration–dependent manner. Flow cytometry and laser confocal microscope studies revealed that the cellular uptake of ACPP-DOX was enhanced after enzymatic-triggered activation and was higher in HT-1080 cells (overexpressed MMPs) than in MCF-7 cells (under-expressed MMPs). The antiproliferative assay showed that ACPP had little toxicity and that ACPP-DOX effectively inhibited HT-1080 cell proliferation. These experiments revealed that the ACPP-DOX conjugate could be triggered by MMP-2/9, which enabled the activated CPP-DOX to enter cells. ACPP-DOX conjugate may be a potential prodrug delivery system used to carry antitumor drugs for MMP-related tumor therapy.Keywords: activable cell-penetrating peptide, matrix metalloproteinase, proteinase-sensitive substrate, cellular uptake, antiproliferative, enzymatic cleavage, tumor extracellular environment |
url |
http://www.dovepress.com/enhancing-cellular-uptake-of-activable-cell-penetrating-peptidendashdo-a9565 |
work_keys_str_mv |
AT shinq enhancingcellularuptakeofactivablecellpenetratingpeptideampndashdoxorubicinconjugatebyenzymaticcleavage AT gaow enhancingcellularuptakeofactivablecellpenetratingpeptideampndashdoxorubicinconjugatebyenzymaticcleavage AT xiangb enhancingcellularuptakeofactivablecellpenetratingpeptideampndashdoxorubicinconjugatebyenzymaticcleavage AT qixr enhancingcellularuptakeofactivablecellpenetratingpeptideampndashdoxorubicinconjugatebyenzymaticcleavage |
_version_ |
1725678198997385216 |