Cargando…
Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro
Adipose-derived stem cells (ADSCs) may be useful as an efficient vehicle in cell-based gene therapy of human diseases due to their ability to migrate to disease lesions. This study investigated the ability of ADSC-harbored human tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) cDNA to...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918625/ https://www.ncbi.nlm.nih.gov/pubmed/27177242 http://dx.doi.org/10.3892/mmr.2016.5283 |
_version_ | 1782439142035030016 |
---|---|
author | JING, HAI XIA DUAN, DE JIAN ZHOU, HUI HU, QING MEI LEI, TIE CHI |
author_facet | JING, HAI XIA DUAN, DE JIAN ZHOU, HUI HU, QING MEI LEI, TIE CHI |
author_sort | JING, HAI XIA |
collection | PubMed |
description | Adipose-derived stem cells (ADSCs) may be useful as an efficient vehicle in cell-based gene therapy of human diseases due to their ability to migrate to disease lesions. This study investigated the ability of ADSC-harbored human tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) cDNA to facilitate TRAIL expression and induce A375 melanoma cell apoptosis as observed using a Transwell co-culture system. A cell migration assay was used to observe ADSC migration ability. In addition, TRAIL protein expression was successfully detected by western blot analysis in ADSCs after stable transfection of TRAIL cDNA. The Transwell co-culture system data showed that TRAIL-ADSCs could induce A375 cell apoptosis in a dose-dependent manner. At the gene level, the killing activity of TRAIL-ADSCs was associated with activation of caspase-4 and caspase-8. Collectively, the data from the current study provides preclinical support of ADSC-facilitated TRAIL expression in the treatment of melanoma. Further investigation is required to evaluate and confirm the in vivo ability of TRAIL-ADSCs in therapy of melanoma in animal models. |
format | Online Article Text |
id | pubmed-4918625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-49186252016-07-11 Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro JING, HAI XIA DUAN, DE JIAN ZHOU, HUI HU, QING MEI LEI, TIE CHI Mol Med Rep Articles Adipose-derived stem cells (ADSCs) may be useful as an efficient vehicle in cell-based gene therapy of human diseases due to their ability to migrate to disease lesions. This study investigated the ability of ADSC-harbored human tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) cDNA to facilitate TRAIL expression and induce A375 melanoma cell apoptosis as observed using a Transwell co-culture system. A cell migration assay was used to observe ADSC migration ability. In addition, TRAIL protein expression was successfully detected by western blot analysis in ADSCs after stable transfection of TRAIL cDNA. The Transwell co-culture system data showed that TRAIL-ADSCs could induce A375 cell apoptosis in a dose-dependent manner. At the gene level, the killing activity of TRAIL-ADSCs was associated with activation of caspase-4 and caspase-8. Collectively, the data from the current study provides preclinical support of ADSC-facilitated TRAIL expression in the treatment of melanoma. Further investigation is required to evaluate and confirm the in vivo ability of TRAIL-ADSCs in therapy of melanoma in animal models. D.A. Spandidos 2016-07 2016-05-13 /pmc/articles/PMC4918625/ /pubmed/27177242 http://dx.doi.org/10.3892/mmr.2016.5283 Text en Copyright: © Jing et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles JING, HAI XIA DUAN, DE JIAN ZHOU, HUI HU, QING MEI LEI, TIE CHI Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title | Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title_full | Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title_fullStr | Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title_full_unstemmed | Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title_short | Adipose-derived mesenchymal stem cell-facilitated TRAIL expression in melanoma treatment in vitro |
title_sort | adipose-derived mesenchymal stem cell-facilitated trail expression in melanoma treatment in vitro |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918625/ https://www.ncbi.nlm.nih.gov/pubmed/27177242 http://dx.doi.org/10.3892/mmr.2016.5283 |
work_keys_str_mv | AT jinghaixia adiposederivedmesenchymalstemcellfacilitatedtrailexpressioninmelanomatreatmentinvitro AT duandejian adiposederivedmesenchymalstemcellfacilitatedtrailexpressioninmelanomatreatmentinvitro AT zhouhui adiposederivedmesenchymalstemcellfacilitatedtrailexpressioninmelanomatreatmentinvitro AT huqingmei adiposederivedmesenchymalstemcellfacilitatedtrailexpressioninmelanomatreatmentinvitro AT leitiechi adiposederivedmesenchymalstemcellfacilitatedtrailexpressioninmelanomatreatmentinvitro |