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Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers

The treatment of cancer such as oligonucleotides or peptides requires efficient delivery systems. A novel peptide, TMTP1, previously derived and identified in our laboratory showed remarkable ability to target highly metastatic tumors both in vitro and in vivo, even at the early stage of occult meta...

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Detalles Bibliográficos
Autores principales: Ma, Xiangyi, Xi, Ling, Luo, Danfeng, Liu, Ronghua, Li, Shu, Liu, Yan, Fan, Liangsheng, Ye, Shuangmei, Yang, Wanhua, Yang, Shuhong, Meng, Li, Zhou, Jianfeng, Wang, Shixuan, Ma, Ding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439480/
https://www.ncbi.nlm.nih.gov/pubmed/22984407
http://dx.doi.org/10.1371/journal.pone.0042685
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author Ma, Xiangyi
Xi, Ling
Luo, Danfeng
Liu, Ronghua
Li, Shu
Liu, Yan
Fan, Liangsheng
Ye, Shuangmei
Yang, Wanhua
Yang, Shuhong
Meng, Li
Zhou, Jianfeng
Wang, Shixuan
Ma, Ding
author_facet Ma, Xiangyi
Xi, Ling
Luo, Danfeng
Liu, Ronghua
Li, Shu
Liu, Yan
Fan, Liangsheng
Ye, Shuangmei
Yang, Wanhua
Yang, Shuhong
Meng, Li
Zhou, Jianfeng
Wang, Shixuan
Ma, Ding
author_sort Ma, Xiangyi
collection PubMed
description The treatment of cancer such as oligonucleotides or peptides requires efficient delivery systems. A novel peptide, TMTP1, previously derived and identified in our laboratory showed remarkable ability to target highly metastatic tumors both in vitro and in vivo, even at the early stage of occult metastasis foci. TMTP1 moderately inhibited tumor cell viability, although not enough to deem it an efficient killer of tumor cells. In this study, we sought to enhance the anti-tumor activity of TMTP1. To do this, we fused it to an antimicrobial peptide, (D)(KLAKLAK)(2), and termed the resulting peptide TMTP1-DKK. We found that TMTP1-DKK could trigger rapid apoptosis in human prostate and gastric cancer cells through both the mitochondrial-induced apoptosis pathway and the death receptor pathway. Furthermore, direct injection of TMTP1-DKK into mice with prostate and gastric xenograft cancers resulted in reduction of tumor volumes and a significant delay in tumor progression and metastasis in vivo. These results suggest that TMTP1-DKK may serve as a powerful therapeutic agent for metastatic tumors.
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spelling pubmed-34394802012-09-14 Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers Ma, Xiangyi Xi, Ling Luo, Danfeng Liu, Ronghua Li, Shu Liu, Yan Fan, Liangsheng Ye, Shuangmei Yang, Wanhua Yang, Shuhong Meng, Li Zhou, Jianfeng Wang, Shixuan Ma, Ding PLoS One Research Article The treatment of cancer such as oligonucleotides or peptides requires efficient delivery systems. A novel peptide, TMTP1, previously derived and identified in our laboratory showed remarkable ability to target highly metastatic tumors both in vitro and in vivo, even at the early stage of occult metastasis foci. TMTP1 moderately inhibited tumor cell viability, although not enough to deem it an efficient killer of tumor cells. In this study, we sought to enhance the anti-tumor activity of TMTP1. To do this, we fused it to an antimicrobial peptide, (D)(KLAKLAK)(2), and termed the resulting peptide TMTP1-DKK. We found that TMTP1-DKK could trigger rapid apoptosis in human prostate and gastric cancer cells through both the mitochondrial-induced apoptosis pathway and the death receptor pathway. Furthermore, direct injection of TMTP1-DKK into mice with prostate and gastric xenograft cancers resulted in reduction of tumor volumes and a significant delay in tumor progression and metastasis in vivo. These results suggest that TMTP1-DKK may serve as a powerful therapeutic agent for metastatic tumors. Public Library of Science 2012-09-11 /pmc/articles/PMC3439480/ /pubmed/22984407 http://dx.doi.org/10.1371/journal.pone.0042685 Text en © 2012 Ma et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ma, Xiangyi
Xi, Ling
Luo, Danfeng
Liu, Ronghua
Li, Shu
Liu, Yan
Fan, Liangsheng
Ye, Shuangmei
Yang, Wanhua
Yang, Shuhong
Meng, Li
Zhou, Jianfeng
Wang, Shixuan
Ma, Ding
Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title_full Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title_fullStr Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title_full_unstemmed Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title_short Anti-Tumor Effects of the Peptide TMTP1-GG-(D)(KLAKLAK)(2) on Highly Metastatic Cancers
title_sort anti-tumor effects of the peptide tmtp1-gg-(d)(klaklak)(2) on highly metastatic cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439480/
https://www.ncbi.nlm.nih.gov/pubmed/22984407
http://dx.doi.org/10.1371/journal.pone.0042685
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