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sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) selectively kills tumor cells and augments chemotherapeutics in vivo. Here, we developed sTRAIL-iRGD, a recombinant protein consisting of sTRAIL fused to CRGDKGPDC, a C-terminal end binding peptide with an integrin-binding arginine-glyc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428854/ https://www.ncbi.nlm.nih.gov/pubmed/28373646 http://dx.doi.org/10.1038/s41598-017-00688-6 |
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author | Huang, Ying Li, Xihan Sha, Huizi Zhang, Lianru Bian, Xinyu Han, Xiao Liu, Baorui |
author_facet | Huang, Ying Li, Xihan Sha, Huizi Zhang, Lianru Bian, Xinyu Han, Xiao Liu, Baorui |
author_sort | Huang, Ying |
collection | PubMed |
description | Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) selectively kills tumor cells and augments chemotherapeutics in vivo. Here, we developed sTRAIL-iRGD, a recombinant protein consisting of sTRAIL fused to CRGDKGPDC, a C-terminal end binding peptide with an integrin-binding arginine-glycine-aspartic acid (iRGD) motif. CRGDKGPDC is a tumor-homing peptide with high penetration into tumor tissue and cells. We found that sTRAIL-iRGD internalized into cultured gastric cancer tumor cells and localized to both the tumor mass in vivo and three-dimensional multicellular spheroids in vitro. sTRAIL-iRGD had an antitumor effect in tumor cell lines, multicellular spheroids and nude mice with tumors. Repeated treatment with sTRAIL-iRGD reduced tumor growth and volume in vivo. Mice treated with sTRAIL-iRGD and paclitaxel (PTX) in combination showed no sign of sTRAIL-iRGD-related liver toxicity. Our data suggest that sTRAIL-iRGD is a promising anti-gastric cancer agent with high selectivity and limited systemic toxicity. |
format | Online Article Text |
id | pubmed-5428854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54288542017-05-15 sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment Huang, Ying Li, Xihan Sha, Huizi Zhang, Lianru Bian, Xinyu Han, Xiao Liu, Baorui Sci Rep Article Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) selectively kills tumor cells and augments chemotherapeutics in vivo. Here, we developed sTRAIL-iRGD, a recombinant protein consisting of sTRAIL fused to CRGDKGPDC, a C-terminal end binding peptide with an integrin-binding arginine-glycine-aspartic acid (iRGD) motif. CRGDKGPDC is a tumor-homing peptide with high penetration into tumor tissue and cells. We found that sTRAIL-iRGD internalized into cultured gastric cancer tumor cells and localized to both the tumor mass in vivo and three-dimensional multicellular spheroids in vitro. sTRAIL-iRGD had an antitumor effect in tumor cell lines, multicellular spheroids and nude mice with tumors. Repeated treatment with sTRAIL-iRGD reduced tumor growth and volume in vivo. Mice treated with sTRAIL-iRGD and paclitaxel (PTX) in combination showed no sign of sTRAIL-iRGD-related liver toxicity. Our data suggest that sTRAIL-iRGD is a promising anti-gastric cancer agent with high selectivity and limited systemic toxicity. Nature Publishing Group UK 2017-04-03 /pmc/articles/PMC5428854/ /pubmed/28373646 http://dx.doi.org/10.1038/s41598-017-00688-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Huang, Ying Li, Xihan Sha, Huizi Zhang, Lianru Bian, Xinyu Han, Xiao Liu, Baorui sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title | sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title_full | sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title_fullStr | sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title_full_unstemmed | sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title_short | sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment |
title_sort | strail-irgd is a promising therapeutic agent for gastric cancer treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428854/ https://www.ncbi.nlm.nih.gov/pubmed/28373646 http://dx.doi.org/10.1038/s41598-017-00688-6 |
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