siRNA-targeted inhibition of growth hormone receptor in human colon cancer SW480 cells

被引:6
作者
Zhou, Dong [1 ]
Yang, Jie [1 ]
Huang, Wei-Dong [1 ]
Wang, Jun [1 ]
Zhang, Qiang [1 ]
机构
[1] Hubei Univ Med, Xiangyang Hosp, Dept Gen Surg, Xiangyang 441000, Hubei Province, Peoples R China
关键词
Growth hormone receptor; Small interfering RNAs; Colon cancer; Gene therapy; Signaling pathway; IGF-BINDING-PROTEINS; ANTAGONIST PEGVISOMANT; COLORECTAL-CANCER; INSULIN; PROLIFERATION; EXPRESSION; INSIGHTS; RISK;
D O I
10.3748/wjg.v19.i44.8108
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To determine the effects of RNAi-mediated inhibition of the growth hormone receptor (GHR) gene on tumors and colon cancer cells in vivo. METHODS: Construction of a eukaryotic vector for human GHR expression, the pcDNA (TM) 6.2-GW/EmGFP-small interfering RNAs (siRNAs)-GHR plasmid, was used to inhibit GHR expression. Thirty-six BALB/c nude mice were randomly divided into groups and treated with normal saline (NS), recombinant plasmid (G2), growth hormone (GH), 5-fluorouracil (FU), G2+FU or G2+FU+GH. Each nude mouse was subcutaneously inoculated with 1x10(7) human colon cancer SW480 cells; the nude mice were weighed before inoculation and on the 2nd, 5th, 8th, 11th, 14th and 17th day after inoculation. All nude mice were sacrificed after 17 d. Each subcutaneous tumor was removed and studied. Tumor volume was measured on the 5th, 8th, 11th, 14th and 17th day after inoculation. The expression of GHR protein in the tumor tissue was detected by Western blotting analy-sis, and the differences in GHR mRNA expression in the tumor tissue were detected by real-time quantitative reverse transcription-polymerase chain reaction. RESULTS: Compared to the control group, the weights of the inoculated nude mice on the 17th day after inoculation were: G2: 21.60 +/- 0.71 g, GH: 21.64 +/- 0.45 g, FU: 18.94 +/- 0.47 g, FU+ G2: 19.40 +/- 0.60 g, G2+ FU+ GH: 21.04 +/- 0.78 g vs NS: 20.68 +/- 0.66 g, P < 0.05; the tumor volumes after the subcutaneous inoculation were: G2: 9.71 +/- 3.82 mm(3), FU: 11.54 +/- 2.42 mm(3), FU+ G2: 11.42 +/- 1.11 mm(3), G2+ FU+ GH: 10.47 +/- 1.02 mm(3) vs NS: 116.81 +/- 10.61 mm(3), P < 0.05. Compared to the GH group, the tumor volumes were significantly decreased in the experimental groups. The GHR protein expression (G2: 0.39 +/- 0.02, FU: 0.40 +/- 0.02, FU+ G2: 0.38 +/- 0.01, G2+ FU+ GH: 0.39 +/- 0.01 vs NS: 0.94 +/- 0.02, P < 0.05) and the GHR mRNA expression (G2: 14.12 +/- 0.10, FU: 15.15 +/- 0.44, FU+ G2: 16.46 +/- 0.27, G2+ FU+ GH: 15.37 +/- 0.57 vs NS: 12.63 +/- 0.14, P < 0.05) were significantly decreased and increased, respectively, in the experimental groups. CONCLUSION: Inhibition of GHR in human colon cancer SW480 cells resulted in anti-tumor effects in nude mice. (C) 2013 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:8108 / 8113
页数:6
相关论文
共 50 条
[31]   Increase of gap junction activities in SW480 human colorectal cancer cells [J].
Bigelow, Kristina ;
Nguyen, Thu A. .
BMC CANCER, 2014, 14
[32]   Profile of protein expression of the colon cancer cell line SW480 with survivin/shRNA [J].
Wang, Xuehu ;
Fu, Zhongxue ;
Zhao, Yu ;
Wu, Xingye ;
Shen, Wei .
EUROPEAN JOURNAL OF CANCER PREVENTION, 2011, 20 (03) :190-198
[33]   Suppressive effects of red ginseng preparations on SW480 colon cancer xenografts in mice [J].
Yang, Goeun ;
Park, Dongsun ;
Lee, Jinsoo ;
Song, Byeng Sub ;
Jeon, Tae Hwan ;
Kang, Shin Jyung ;
Jeon, Jeong Hee ;
Shin, Sunhee ;
Jeong, Heon-Sang ;
Lee, Hwa-Jeong ;
Kim, Yun-Bae .
FOOD SCIENCE AND BIOTECHNOLOGY, 2011, 20 (06) :1649-1653
[34]   Quercetin Inhibit Human SW480 Colon Cancer Growth in Association with Inhibition of Cyclin D1 and Survivin Expression through Wnt/-Catenin Signaling Pathway [J].
Shan, Bao-En ;
Wang, Ming-Xia ;
Li, Run-qing .
CANCER INVESTIGATION, 2009, 27 (06) :604-612
[35]   Curcumin combining with si-MALAT1 inhibits the invasion and migration of colon cancer SW480 cells [J].
Wei, Dai ;
Yun, Li Shi ;
Xiao Dejun ;
Cong, Liu ;
He, Jin-Hua ;
Yan, Lin .
BRAZILIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 55
[36]   Low-dose heparin treatment does not inhibit SW480 human colon cancer growth and metastasis in vivo [J].
Antachopoulos, CT ;
Gagos, S ;
Iliopoulos, DC ;
Karayannacos, PE ;
TseleniBalafouta, S ;
Alevras, P ;
Koundouris, C ;
Skalkeas, GD .
IN VIVO, 1996, 10 (05) :527-531
[37]   Quercetin, a potent inhibitor against β-catenin/Tcf signaling in SW480 colon cancer cells [J].
Park, CH ;
Chang, JY ;
Hahm, ER ;
Park, S ;
Kim, HK ;
Yang, CH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 328 (01) :227-234
[38]   Demonstration of dose dependent cytotoxic activity in SW480 colon cancer cells by 177Lu-labeled siRNA targeting IGF-1R [J].
Fathi, Mojtaba ;
Taghikhani, Mohammad ;
Ghannadi-Margheh, Mohammad ;
Yavari, Kamal .
NUCLEAR MEDICINE AND BIOLOGY, 2013, 40 (04) :529-536
[39]   Gene expression profile of cancer stem-like cells in the SW480 colon adenocarcinoma cell line [J].
Wang, Yuanyuan ;
Zhou, Ling ;
Qing, Qing ;
Li, Yingfei ;
Li, Lixuan ;
Dong, Xiaoying ;
Xiao, Bing .
ONCOLOGY REPORTS, 2019, 42 (01) :386-398
[40]   Anti-proliferation effect of zoledronic acid on human colon cancer line SW480 [J].
Han, Fu-Shi ;
Lin, Mou-Bin ;
Zhu, Hui-Yuan ;
Chen, Ying-Qun ;
Shui, Wei ;
Xu, Jin-Ming .
ASIAN PACIFIC JOURNAL OF TROPICAL MEDICINE, 2016, 9 (02) :164-168