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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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. |
format | Online Article Text |
id | pubmed-5021025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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