Cargando…

Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets

Colon cancer (CC) belongs to the three major malignancies with a high recurrence rate. Therefore, a novel drug delivery system that can prevent CC recurrence while minimizing side effects is needed. Tumor-necrosis-factor-related apoptosis-inducing ligand (TRAIL) has recently been spotlighted as a pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Sungjun, Jwa, Yerim, Hong, Jiyeon, Kim, Kyobum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319433/
https://www.ncbi.nlm.nih.gov/pubmed/35877512
http://dx.doi.org/10.3390/gels8070427
_version_ 1784755547997732864
author Kim, Sungjun
Jwa, Yerim
Hong, Jiyeon
Kim, Kyobum
author_facet Kim, Sungjun
Jwa, Yerim
Hong, Jiyeon
Kim, Kyobum
author_sort Kim, Sungjun
collection PubMed
description Colon cancer (CC) belongs to the three major malignancies with a high recurrence rate. Therefore, a novel drug delivery system that can prevent CC recurrence while minimizing side effects is needed. Tumor-necrosis-factor-related apoptosis-inducing ligand (TRAIL) has recently been spotlighted as a protein drug that can induce apoptosis of cancer cells specifically. However, its short in vivo half-life is still a challenge to overcome. Hence, in this study, a gel-like mPEGylated coacervate (mPEG-Coa) delivery platform was developed through electrostatic interaction of mPEG-poly(ethylene arginylaspartate diglyceride) (mPEG-PEAD) and heparin for effective protection of cargo TRAIL, subsequently preserving its bioactivity. mPEG-Coa could protect cargo TRAIL against protease. Sustained release was observed for a long-term (14 days). In addition, recurrence of HCT-116 cells was suppressed when cells were treated with TRAIL-loaded mPEG-Coa for 7 days through long-term continuous supply of active TRAIL, whereas re-proliferation occurred in the bolus TRAIL-treated group. Taken together, these results suggest that our gel-like mPEG-Coa could be utilized as a functional delivery platform to suppress CC recurrence by exogenously supplying TRAIL for a long time with a single administration.
format Online
Article
Text
id pubmed-9319433
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93194332022-07-27 Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets Kim, Sungjun Jwa, Yerim Hong, Jiyeon Kim, Kyobum Gels Article Colon cancer (CC) belongs to the three major malignancies with a high recurrence rate. Therefore, a novel drug delivery system that can prevent CC recurrence while minimizing side effects is needed. Tumor-necrosis-factor-related apoptosis-inducing ligand (TRAIL) has recently been spotlighted as a protein drug that can induce apoptosis of cancer cells specifically. However, its short in vivo half-life is still a challenge to overcome. Hence, in this study, a gel-like mPEGylated coacervate (mPEG-Coa) delivery platform was developed through electrostatic interaction of mPEG-poly(ethylene arginylaspartate diglyceride) (mPEG-PEAD) and heparin for effective protection of cargo TRAIL, subsequently preserving its bioactivity. mPEG-Coa could protect cargo TRAIL against protease. Sustained release was observed for a long-term (14 days). In addition, recurrence of HCT-116 cells was suppressed when cells were treated with TRAIL-loaded mPEG-Coa for 7 days through long-term continuous supply of active TRAIL, whereas re-proliferation occurred in the bolus TRAIL-treated group. Taken together, these results suggest that our gel-like mPEG-Coa could be utilized as a functional delivery platform to suppress CC recurrence by exogenously supplying TRAIL for a long time with a single administration. MDPI 2022-07-08 /pmc/articles/PMC9319433/ /pubmed/35877512 http://dx.doi.org/10.3390/gels8070427 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Sungjun
Jwa, Yerim
Hong, Jiyeon
Kim, Kyobum
Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title_full Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title_fullStr Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title_full_unstemmed Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title_short Inhibition of Colon Cancer Recurrence via Exogenous TRAIL Delivery Using Gel-like Coacervate Microdroplets
title_sort inhibition of colon cancer recurrence via exogenous trail delivery using gel-like coacervate microdroplets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319433/
https://www.ncbi.nlm.nih.gov/pubmed/35877512
http://dx.doi.org/10.3390/gels8070427
work_keys_str_mv AT kimsungjun inhibitionofcoloncancerrecurrenceviaexogenoustraildeliveryusinggellikecoacervatemicrodroplets
AT jwayerim inhibitionofcoloncancerrecurrenceviaexogenoustraildeliveryusinggellikecoacervatemicrodroplets
AT hongjiyeon inhibitionofcoloncancerrecurrenceviaexogenoustraildeliveryusinggellikecoacervatemicrodroplets
AT kimkyobum inhibitionofcoloncancerrecurrenceviaexogenoustraildeliveryusinggellikecoacervatemicrodroplets