Chondroitin sulfate-functionalized polyamidoamine-mediated miR-34a delivery for inhibiting the proliferation and migration of pancreatic cancer

被引:14
作者
Duan, Yan [1 ]
Xing, Zhen [1 ]
Yang, Jiebing [1 ]
Wang, Yudi [1 ]
Chen, Jiawen [1 ]
Zhang, Yan [1 ]
Shi, Wei [1 ]
Li, Quanshun [1 ]
机构
[1] Jilin Univ, Sch Life Sci, Minist Educ, Key Lab Mol Enzymol & Engn, Changchun 130012, Peoples R China
关键词
HYALURONIC-ACID; GENE; POLYETHYLENIMINE; DENDRIMERS; NANOPARTICLES; MICRORNA-34A; METASTASIS; THERAPY; DRUG;
D O I
10.1039/c6ra15716e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, chondroitin sulfate-functionalized polyamidoamine (CS-PAMAM) was employed as a carrier in miR-34a delivery, and the inhibition of cell proliferation and migration of pancreatic cancer was systematically evaluated, using human pancreatic carcinoma cell line MiaPaCa-2 as a model. Through confocal laser scanning microscopy, an efficient cellular uptake of CS-PAMAM/miR-34a nanoparticles has been demonstrated to be executed in a CD44-dependent manner. After the successful delivery of miR-34a, the cell proliferation could be obviously inhibited due to the activation of cell apoptosis and cell cycle arrest. Meanwhile, CS-PAMAM-mediated miR-34a delivery could realize the suppression of cell migration elucidated by wound healing and transwell migration assays. Thus, the derivative CS-PAMAM could potentially be used as an effective carrier for miR-34a delivery to achieve the tumor gene therapy.
引用
收藏
页码:70870 / 70876
页数:7
相关论文
共 29 条
  • [11] The miR-34 family in cancer and apoptosis
    Hermeking, H.
    [J]. CELL DEATH AND DIFFERENTIATION, 2010, 17 (02) : 193 - 199
  • [12] MicroRNA Molecular Profiles Associated with Diagnosis, Clinicopathologic Criteria, and Overall Survival in Patients with Resectable Pancreatic Ductal Adenocarcinoma
    Jamieson, Nigel B.
    Morran, Douglas C.
    Morton, Jennifer P.
    Ali, Asif
    Dickson, Euan J.
    Carter, C. Ross
    Sansom, Owen J.
    Evans, T. R. Jeffry
    McKay, Colin J.
    Oien, Karin A.
    [J]. CLINICAL CANCER RESEARCH, 2012, 18 (02) : 534 - 545
  • [13] Jemal A, 2009, CA-CANCER J CLIN, V59, P225, DOI [10.3322/caac.20006, 10.3322/caac.21254, 10.3322/caac.21332, 10.3322/caac.21551, 10.3322/caac.20073, 10.3322/caac.21387, 10.3322/caac.21654, 10.3322/caac.21601]
  • [14] Designing dendrimers for biological applications
    Lee, CC
    MacKay, JA
    Fréchet, JMJ
    Szoka, FC
    [J]. NATURE BIOTECHNOLOGY, 2005, 23 (12) : 1517 - 1526
  • [15] Polymeric Nanocarriers for Non-Viral Gene Delivery
    Li, Ling
    Wei, Yuquan
    Gong, Changyang
    [J]. JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2015, 11 (05) : 739 - 770
  • [16] MicroRNA Targeted Therapeutic Approach for Pancreatic Cancer
    Li, Yiwei
    Sarkar, Fazlul H.
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2016, 12 (03): : 326 - 337
  • [17] Guanidinated Thiourea-Decorated Polyethylenimines for Enhanced Membrane Penetration and Efficient siRNA Delivery
    Li, Yuce
    Tian, Huayu
    Ding, Jianxun
    Lin, Lin
    Chen, Jie
    Gao, Shiqian
    Chen, Xuesi
    [J]. ADVANCED HEALTHCARE MATERIALS, 2015, 4 (09) : 1369 - 1375
  • [18] Inhibition of cell proliferation and migration by chondroitin sulfate-g-polyethylenimine-mediated miR-34a delivery
    Liang, Shaojun
    Duan, Yan
    Xing, Zhen
    Han, Haobo
    Zhang, Aijun
    Li, Li
    Yang, Yan
    Li, Quanshun
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 2015, 136 : 577 - 584
  • [19] Preparation of Chondroitin Sulfate-g-poly(ε-caprolactone) Copolymers as a CD44-Targeted Vehicle for Enhanced Intracellular Uptake
    Liu, Yu-Sheng
    Chiu, Chien-Chih
    Chen, Hsuan-Ying
    Chen, Su-Hwei
    Wang, Li-Fang
    [J]. MOLECULAR PHARMACEUTICS, 2014, 11 (04) : 1164 - 1175
  • [20] Chondroitin sulfate-polyethylenimine copolymer-coated superparamagnetic iron oxide nanoparticles as an efficient magneto-gene carrier for microRNA-encoding plasmid DNA delivery
    Lo, Yu-Lun
    Chou, Han-Lin
    Liao, Zi-Xian
    Huang, Shih-Jer
    Ke, Jyun-Han
    Liu, Yu-Sheng
    Chiu, Chien-Chih
    Wang, Li-Fang
    [J]. NANOSCALE, 2015, 7 (18) : 8554 - 8565