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Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer

Nek2 (NIMA‐related kinase 2) is a serine‐threonine kinase and human homolog of the mitotic regulator NIMA of Aspergillus nidulan. We reported the efficiency of Nek2 siRNA in several cancer xenograft models using cholangiocarcinoma, breast cancer and colorectal cancer. Pancreatic cancer is difficult...

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Autores principales: Kokuryo, Toshio, Hibino, Shigeru, Suzuki, Kazushi, Watanabe, Katsutaka, Yokoyama, Yukihiro, Nagino, Masato, Senga, Takeshi, Hamaguchi, Michinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021025/
https://www.ncbi.nlm.nih.gov/pubmed/27316377
http://dx.doi.org/10.1111/cas.12993
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author Kokuryo, Toshio
Hibino, Shigeru
Suzuki, Kazushi
Watanabe, Katsutaka
Yokoyama, Yukihiro
Nagino, Masato
Senga, Takeshi
Hamaguchi, Michinari
author_facet Kokuryo, Toshio
Hibino, Shigeru
Suzuki, Kazushi
Watanabe, Katsutaka
Yokoyama, Yukihiro
Nagino, Masato
Senga, Takeshi
Hamaguchi, Michinari
author_sort Kokuryo, Toshio
collection PubMed
description Nek2 (NIMA‐related kinase 2) is a serine‐threonine kinase and human homolog of the mitotic regulator NIMA of Aspergillus nidulan. We reported the efficiency of Nek2 siRNA in several cancer xenograft models using cholangiocarcinoma, breast cancer and colorectal cancer. Pancreatic cancer is difficult to treat due to its rapid progression and resistance to chemotherapy. Novel treatments are urgently required to improve survival in pancreatic cancer, and siRNA are a promising therapeutic option. However, finding an in vivo drug delivery system of siRNA remains a major problem for clinical application. In this study, the overexpression of Nek2 was identified in pancreatic cancer cell lines. Nek2 siRNA inhibited tumor growth in a subcutaneous xenograft mouse model of pancreatic cancer, prolonged the survival time in an intraperitoneal xenograft mouse model and efficiently prevented the progression of liver metastasis using a portal venous port–catheter system. Taken together, Nek2 is an effective therapeutic target in pancreatic cancer. An adequate delivery system is considered important in treating advanced pancreatic cancer, such as peritoneal dissemination and liver metastasis. Further investigations are required on the safety and side effects of the portal venous port–catheter system. We hope that Nek2 siRNA will be a novel therapeutic strategy for pancreatic cancer with liver metastasis and peritoneal dissemination.
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spelling pubmed-50210252016-09-20 Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer Kokuryo, Toshio Hibino, Shigeru Suzuki, Kazushi Watanabe, Katsutaka Yokoyama, Yukihiro Nagino, Masato Senga, Takeshi Hamaguchi, Michinari Cancer Sci Original Articles Nek2 (NIMA‐related kinase 2) is a serine‐threonine kinase and human homolog of the mitotic regulator NIMA of Aspergillus nidulan. We reported the efficiency of Nek2 siRNA in several cancer xenograft models using cholangiocarcinoma, breast cancer and colorectal cancer. Pancreatic cancer is difficult to treat due to its rapid progression and resistance to chemotherapy. Novel treatments are urgently required to improve survival in pancreatic cancer, and siRNA are a promising therapeutic option. However, finding an in vivo drug delivery system of siRNA remains a major problem for clinical application. In this study, the overexpression of Nek2 was identified in pancreatic cancer cell lines. Nek2 siRNA inhibited tumor growth in a subcutaneous xenograft mouse model of pancreatic cancer, prolonged the survival time in an intraperitoneal xenograft mouse model and efficiently prevented the progression of liver metastasis using a portal venous port–catheter system. Taken together, Nek2 is an effective therapeutic target in pancreatic cancer. An adequate delivery system is considered important in treating advanced pancreatic cancer, such as peritoneal dissemination and liver metastasis. Further investigations are required on the safety and side effects of the portal venous port–catheter system. We hope that Nek2 siRNA will be a novel therapeutic strategy for pancreatic cancer with liver metastasis and peritoneal dissemination. John Wiley and Sons Inc. 2016-08-12 2016-09 /pmc/articles/PMC5021025/ /pubmed/27316377 http://dx.doi.org/10.1111/cas.12993 Text en © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, 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 Original Articles
Kokuryo, Toshio
Hibino, Shigeru
Suzuki, Kazushi
Watanabe, Katsutaka
Yokoyama, Yukihiro
Nagino, Masato
Senga, Takeshi
Hamaguchi, Michinari
Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title_full Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title_fullStr Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title_full_unstemmed Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title_short Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
title_sort nek2 sirna therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021025/
https://www.ncbi.nlm.nih.gov/pubmed/27316377
http://dx.doi.org/10.1111/cas.12993
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