z-logo
open-access-imgOpen Access
Nek2 siRNA therapy using a portal venous port–catheter system for liver metastasis in pancreatic cancer
Author(s) -
Kokuryo Toshio,
Hibino Shigeru,
Suzuki Kazushi,
Watanabe Katsutaka,
Yokoyama Yukihiro,
Nagino Masato,
Senga Takeshi,
Hamaguchi Michinari
Publication year - 2016
Publication title -
cancer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 1347-9032
DOI - 10.1111/cas.12993
Subject(s) - pancreatic cancer , medicine , metastasis , cancer research , cancer , liver cancer , oncology
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 si RNA 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 si RNA are a promising therapeutic option. However, finding an in vivo drug delivery system of si RNA remains a major problem for clinical application. In this study, the overexpression of Nek2 was identified in pancreatic cancer cell lines. Nek2 si RNA 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 si RNA will be a novel therapeutic strategy for pancreatic cancer with liver metastasis and peritoneal dissemination.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here