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Macrophage migration inhibitory factor siRNA inhibits hepatic metastases of colorectal cancer cells.
Wu, Li-Hao; Xia, Harry Hua-Xiang; Ma, Wei-Qing; Zhong, Hao-Jie; Xu, Hui-Xian; Wang, Ya-Min; Yang, Rong-Jiao; Wang, Li-Jing; Chen, Yu; Li, Lan; He, Xing-Xiang.
Affiliation
  • Wu LH; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Xia HH; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Ma WQ; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Zhong HJ; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Xu HX; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Wang YM; Department of Gastroenterology, The 101 Hospital of the Chinese People\'s Liberation Army, Wuxi, Jiangsu 214000, China.
  • Yang RJ; Department of Gastroenterology, Qingyuan Renmin Hospital, Qingyuan, Guangdong 511500, China.
  • Wang LJ; Institute of Vascular Biology, Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Chen Y; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • Li L; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong 510080, China.
  • He XX; Department of Gastroenterology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou 510080, Guangdong, China, 13724887928@qq.com.
Front Biosci (Landmark Ed) ; 22(8): 1365-1378, 2017 03 01.
Article in En | MEDLINE | ID: mdl-28199208
The purpose of this study was to assess the anti-tumor effects of macrophage migration inhibitory factor (MIF) siRNA on colorectal cancer in a mouse xenograft model. MIF specific siRNA (MIF siRNA) or a nonspecific control siRNA was introduced to murine colorectal cancer CT-26 cells. Mouse xenograft models of colorectal cancer were established. MIF siRNA, control siRNA or water was injected twice a week intravenously for 4 weeks. MIF siRNA inhibited the proliferation and migration, while induced apoptosis of CT-26 cells in vitro. Injection of MIF siRNA resulted in a significant decrease of serum MIF and VEGF levels, and the weight and volume of cecum-grafted tumors in vivo. In contrast, the number of apoptotic cells and caspase-3 expression were increased by MIF siRNA in cecum graft tumor tissues. Moreover, the water and fodder consumption were significantly improved by MIF siRNA treatment. Importantly, MIF siRNA reduced the hepatic metastases from colorectal cancer. Our results suggest that siRNA targeting MIF is a promising agent for the treatment of hepatic metastasis of colorectal cancer cells.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Macrophage Migration-Inhibitory Factors / Intramolecular Oxidoreductases / Liver Neoplasms, Experimental Type of study: Prognostic_studies Limits: Animals Language: En Journal: Front Biosci (Landmark Ed) Year: 2017 Document type: Article Affiliation country: Country of publication:
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Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Macrophage Migration-Inhibitory Factors / Intramolecular Oxidoreductases / Liver Neoplasms, Experimental Type of study: Prognostic_studies Limits: Animals Language: En Journal: Front Biosci (Landmark Ed) Year: 2017 Document type: Article Affiliation country: Country of publication: