Assessment of MMP29 Gene Expression and Silver Nanoparticles Effects on Colon Cancer Cell Line (HT29)

被引:3
作者
Ali, Alaa Naseer Mohammed [1 ]
Kareem, Sawsan Mohammed [2 ]
Ghasemian, Abdolmajid [3 ]
机构
[1] Mustansiryiah Univ, Coll Sci, Dept Biol, Baghdad, Iraq
[2] Mustansiryah Univ, Coll Sci, Biol Dept, Baghdad, Iraq
[3] Islamic Azad Univ, Dept Biol, Cent Tehran Branch, Tehran, Iran
关键词
AgNPs; HT29; Matrix metalloproteinase 9; Colon Cancer; Cytotoxicity; MATRIX METALLOPROTEINASES; GOLD NANOPARTICLES; TISSUE INHIBITORS; ANTIBACTERIAL; ANTIOXIDANT; MMP-9;
D O I
10.1007/s12029-019-00289-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Colon cancer is a major cause of death around the world. The evaluation of novel approaches on corresponding genes would be a vital strategy toward eradication of cancer cells. In this study, the toxicity of silver nanoparticle on the colon cancer cell line (HT29) and expression of matrix metalloproteinase (MMP29) gene was investigated. Materials and Methods The silver nanoparticle (AgNPs) was synthesized and assessed by transmission electron microscopy (TEM). The cytotoxicity of synthesized AgNP on the HT29 cell line was evaluated using the MTT assay. Furthermore, the expression of MMP29 gene was investigated by the quantitative real-time PCR (RT-qPCR). Results The TEM results revealed that the fabricated AgNPs were mostly spherical in shape and had an average diameter of 22 nm. The results outlined that AgNPs significantly decreased the viability of cells in a dose- and time-dependent manner (p < 0.001). Additionally, we observed a significant difference among various concentrations. Conclusion The findings indicated that the green fabricated AgNPs have the potential as a promising approach toward the colon cancer therapy. Furthered studies are essential to evaluate against other cancer cell lines and genes participating in the cancer progress.
引用
收藏
页码:560 / 563
页数:4
相关论文
共 24 条
[1]   Green synthesis of multifunctional silver and gold nanoparticles from the oriental herbal adaptogen: Siberian ginseng [J].
Abbai, Ragavendran ;
Mathiyalagan, Ramya ;
Markus, Josua ;
Kim, Yeon-Ju ;
Wang, Chao ;
Singh, Priyanka ;
Ahn, Sungeun ;
Farh, Mohamed El-Agamy ;
Yang, Deok Chun .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2016, 11 :3131-3143
[2]   Matrix metalloproteinase levels are elevated in inflammatory bowel disease [J].
Baugh, MD ;
Perry, MJ ;
Hollander, AP ;
Davies, DR ;
Cross, SS ;
Lobo, AJ ;
Taylor, CJ ;
Evans, GS .
GASTROENTEROLOGY, 1999, 117 (04) :814-822
[3]   Biosynthesis of gold nanoparticles by biosorption using Magnetospirillum gryphiswaldense MSR-1 [J].
Cai, Fang ;
Li, Jing ;
Sun, Jinsheng ;
Ji, Yulan .
CHEMICAL ENGINEERING JOURNAL, 2011, 175 :70-75
[4]   Jun N-terminal kinase 1 mediates transcriptional induction of matrix metalloproteinase 9 expression [J].
Crowe, DL ;
Tsang, KJ ;
Shemirani, B .
NEOPLASIA, 2001, 3 (01) :27-32
[5]  
Devi J.S., 2012, Open Access Sci Rep, V1, P242, DOI 10.4172/scientificreports.242
[6]   New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[7]   Serum levels of matrix metalloproteinase-2 and-9 and conventional tumor markers (CEA and CA 19-9) in patients with colorectal and gastric cancers [J].
Emara, Marwan ;
Cheung, Po-Yin ;
Grabowski, Krzysztof ;
Sawicki, Grzegorz ;
Wozniak, Mietek .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2009, 47 (08) :993-1000
[8]   Role of cadherins and matrixins in melanoma [J].
Gruss, C ;
Herlyn, M .
CURRENT OPINION IN ONCOLOGY, 2001, 13 (02) :117-123
[9]  
Khatami M., 2017, TEHRAN U MED J, V75, P72
[10]   Altered plasma matrix metalloproteinase-9/tissue metalloproteinase-1 concentration during the early postoperative period in patients with colorectal cancer [J].
Kirman, I ;
Jain, S ;
Cekic, V ;
Belizon, A ;
Balik, E ;
Sylla, P ;
Arnell, T ;
Forde, K ;
Whelan, RL .
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2006, 20 (03) :482-486