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The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5

Goat peroxiredoxin-5 (gPRDX5) was verified as a good anti-cancer bioactive peptide (ACBP) against different tumor cell lines. Considering the immunogenicity between species for further therapeutic application, it is necessary to similarly investigate the antitumor activity of human peroxiredoxin-5 (...

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Autores principales: Liu, Juanjuan, Feng, Xiaozhou, Jin, Yuanyuan, Sun, Zhengyang, Meng, Haoyi, Zhang, Zhifei, Hu, Laixing, Yang, Zhaoyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432328/
https://www.ncbi.nlm.nih.gov/pubmed/28423711
http://dx.doi.org/10.18632/oncotarget.16089
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author Liu, Juanjuan
Feng, Xiaozhou
Jin, Yuanyuan
Sun, Zhengyang
Meng, Haoyi
Zhang, Zhifei
Hu, Laixing
Yang, Zhaoyong
author_facet Liu, Juanjuan
Feng, Xiaozhou
Jin, Yuanyuan
Sun, Zhengyang
Meng, Haoyi
Zhang, Zhifei
Hu, Laixing
Yang, Zhaoyong
author_sort Liu, Juanjuan
collection PubMed
description Goat peroxiredoxin-5 (gPRDX5) was verified as a good anti-cancer bioactive peptide (ACBP) against different tumor cell lines. Considering the immunogenicity between species for further therapeutic application, it is necessary to similarly investigate the antitumor activity of human peroxiredoxin-5 (hPRDX5) with 89% similarity in sequence to gPRDX5. In order to evaluate its antitumor activity, the potential anti-neoplastic effect of hPRDX5 on a mouse model was observed directly. The results of its in vivo antitumor activity suggested that hPRDX5 could resist immunosuppression by promoting lymphocyte proliferation and up-regulating the levels of serum cytokines. Meanwhile, PD-L1 was speculated as one of the targets of hPRDX5 to inhibit tumor by enhancing the immune activity according to a preliminary molecular docking study on the interactions between hPRDX5 and PD-L1. The modeling provides a basis for structural modification on hPRDX5/PD-L1 for further biological and biochemical study on the pathway blocking mechanism of hPRDX5. In this work, the results demonstrate that hPRDX5 displays efficient antitumor and immunoregulatory properties in the colon cancer C26/BALB/c and melanoma B16/C57Bl/6 mice tumor models, and suggest the potential of developing peptides from hPRDX5 as low molecular weight drug candidates for corresponding cancer immunotherapy.
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spelling pubmed-54323282017-05-17 The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5 Liu, Juanjuan Feng, Xiaozhou Jin, Yuanyuan Sun, Zhengyang Meng, Haoyi Zhang, Zhifei Hu, Laixing Yang, Zhaoyong Oncotarget Research Paper Goat peroxiredoxin-5 (gPRDX5) was verified as a good anti-cancer bioactive peptide (ACBP) against different tumor cell lines. Considering the immunogenicity between species for further therapeutic application, it is necessary to similarly investigate the antitumor activity of human peroxiredoxin-5 (hPRDX5) with 89% similarity in sequence to gPRDX5. In order to evaluate its antitumor activity, the potential anti-neoplastic effect of hPRDX5 on a mouse model was observed directly. The results of its in vivo antitumor activity suggested that hPRDX5 could resist immunosuppression by promoting lymphocyte proliferation and up-regulating the levels of serum cytokines. Meanwhile, PD-L1 was speculated as one of the targets of hPRDX5 to inhibit tumor by enhancing the immune activity according to a preliminary molecular docking study on the interactions between hPRDX5 and PD-L1. The modeling provides a basis for structural modification on hPRDX5/PD-L1 for further biological and biochemical study on the pathway blocking mechanism of hPRDX5. In this work, the results demonstrate that hPRDX5 displays efficient antitumor and immunoregulatory properties in the colon cancer C26/BALB/c and melanoma B16/C57Bl/6 mice tumor models, and suggest the potential of developing peptides from hPRDX5 as low molecular weight drug candidates for corresponding cancer immunotherapy. Impact Journals LLC 2017-03-10 /pmc/articles/PMC5432328/ /pubmed/28423711 http://dx.doi.org/10.18632/oncotarget.16089 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Liu, Juanjuan
Feng, Xiaozhou
Jin, Yuanyuan
Sun, Zhengyang
Meng, Haoyi
Zhang, Zhifei
Hu, Laixing
Yang, Zhaoyong
The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title_full The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title_fullStr The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title_full_unstemmed The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title_short The antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
title_sort antitumor activity and preliminary modeling on the potential mechanism of action of human peroxiredoxin-5
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432328/
https://www.ncbi.nlm.nih.gov/pubmed/28423711
http://dx.doi.org/10.18632/oncotarget.16089
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