Targeting lung cancer initiating cells by all-trans retinoic acid-loaded lipid-PLGA nanoparticles with CD133 aptamers

被引:18
|
作者
Zhang, Yu [1 ]
Zhao, Juan [1 ]
Sun, Jing [2 ]
Huang, Lu [1 ]
Li, Qingfeng [1 ]
机构
[1] Hubei Univ Arts & Sci, Dept Oncol, Xiangyang Cent Hosp, Affiliated Hosp, 136 Jingzhou St, Xiangyang 441000, Hubei, Peoples R China
[2] Second Mil Med Univ, Dept Pharm, Shanghai 200433, Peoples R China
关键词
lung cancer; cancer initiating cells; nanoparticles; CD133; aptamers;
D O I
10.3892/etm.2018.6762
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Lung cancer initiating cells represent a specific subpopulation of lung cancer cells, which significantly contribute to the initiation, metastasis and recurrence of lung cancer. CD133, initially considered a marker of stem cells, is now considered as a marker for lung cancer initiating cells. All-trans retinoic acid (RA) has been demonstrated to cause the differentiation, inhibition of proliferation, and apoptosis of cancer cells and cancer initiating cells. However, there have been no reports on the activity of RA against lung cancer initiating cells. In the present study, the activity of RA against lung cancer initiating cells was investigated by determining the cytotoxicity, and performing a tumorsphere assay and flow cytometry-based analysis. In addition, to promote the therapeutic effect of RA in CD133(+) lung cancer initiating cells, RA-loaded lipid poly(lactic-co-glycolic acid) (PLGA) nanoparticles with CD133 aptamers (RA-LPNPs-CD133) were developed. The activity of RA and RA-LPNPs-CD133 against lung cancer initiating cells was also investigated. RA-LPNPs-CD133 had a size of 129.9 nm, and exhibited sustained release of RA during the 144-h period. For the first time, to the best of our knowledge, the present study demonstrated that RA exerted potent activity towards CD133(+) lung cancer initiating cells. The results also showed that RA-LPNPs-CD133 efficiently and specifically promoted the delivery of RA to CD133(+) lung cancer initiating cells, exhibiting superior inhibitory effects against CD133(+) lung cancer initiating cells compared with non-targeted nanoparticles and RA. To the best of our knowledge, the present study is the first to report the promotion of RA delivery via nanoparticles to lung cancer initiating cells and achievement of a superior inhibitory effect against lung cancer initiating cells by the utilization of CD133 aptamers. Therefore, RA-LPNPs-CD133 represents a promising tool for the elimination of lung cancer initiating cells.
引用
收藏
页码:4639 / 4649
页数:11
相关论文
共 41 条
  • [1] Lipid-polymer nanoparticles with CD133 aptamers for targeted delivery of all-trans retinoic acid to osteosarcoma initiating cells
    Gui, Keke
    Zhang, Xinchao
    Chen, Fangyi
    Ge, Zhe
    Zhang, Shichao
    Qi, Xiaoxia
    Sun, Jing
    Yu, Zuochong
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2019, 111 : 751 - 764
  • [2] All-trans retinoic acid-loaded lipid nanoparticles as a transdermal drug delivery carrier
    Charoenputtakhun, Ponwanit
    Opanasopit, Praneet
    Rojanarata, Theerasak
    Ngawhirunpat, Tanasait
    [J]. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2014, 19 (02) : 164 - 172
  • [3] Experimental design and characterization of dual-antibody-conjugated all-trans retinoic acid-loaded lipid nanoparticles as a potential cancer therapy
    Islek, Zeynep
    Sagiroglu, Ali Asram
    Ucisik, Mehmet Hikmet
    Kirbas, Oguz Kaan
    Demirel, Erhan
    Yurdasiper, Aysu
    Sahin, Fikrettin
    Ozer, Ozgen
    [J]. JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2024, 100
  • [4] Anticancer activity of all-trans retinoic acid-loaded liposomes on human thyroid carcinoma cells
    Cristiano, Maria Chiara
    Cosco, Donato
    Celia, Christian
    Tudose, Andra
    Mare, Rosario
    Paolino, Donatella
    Fresta, Massimo
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 2017, 150 : 408 - 416
  • [5] Temperature-controlled continuous production of all-trans retinoic acid-loaded solid lipid nanoparticles using static mixers
    Shao, Wenyao
    Yan, Mengwen
    Chen, Tingting
    Chen, Yuqing
    Xiao, Zongyuan
    [J]. MATERIALS RESEARCH EXPRESS, 2017, 4 (04):
  • [6] Comedolytic effect and reduced skin irritation of a new formulation of all-trans retinoic acid-loaded solid lipid nanoparticles for topical treatment of acne
    G. A. Castro
    C. A. Oliveira
    G. A. B. Mahecha
    L. A. M. Ferreira
    [J]. Archives of Dermatological Research, 2011, 303 : 513 - 520
  • [7] Comedolytic effect and reduced skin irritation of a new formulation of all-trans retinoic acid-loaded solid lipid nanoparticles for topical treatment of acne
    Castro, G. A.
    Oliveira, C. A.
    Mahecha, G. A. B.
    Ferreira, L. A. M.
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2011, 303 (07) : 513 - 520
  • [8] Enhanced targeting of prostate cancer-initiating cells by salinomycin-encapsulated lipid-PLGA nanoparticles linked with CD44 antibodies
    Wei, Jun
    Sun, Jin
    Liu, Yu
    [J]. ONCOLOGY LETTERS, 2019, 17 (04) : 4024 - 4033
  • [9] Formulation parameters determining the physicochemical characteristics of solid lipid nanoparticles loaded with all-trans retinoic acid
    Lim, SJ
    Kim, CK
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 243 (1-2) : 135 - 146
  • [10] Dual-targeting nanomicelles with CD133 and CD44 aptamers for enhanced delivery of gefitinib to two populations of lung cancer-initiating cells
    Huang, Xiaolong
    Wan, Jun
    Leng, Dewen
    Zhang, Yingying
    Yang, Shuo
    [J]. EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2020, 19 (01) : 192 - 204