Improved delivery of miR-1296 loaded cationic nanoliposomes for effective suppression of triple negative breast cancer

被引:20
作者
Albakr, Lamyaa [1 ]
Alqahtani, Fulwah Yahya [1 ]
Aleanizy, Fadilah Sfouq [1 ]
Alomrani, Abdullah [1 ]
Badran, Mohammad [1 ]
Alhindas, Hussein [2 ]
Al-Mohanna, Futwan [2 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Cell Biol, Riyadh, Saudi Arabia
关键词
miR-1296; Liposomes; Triple-negative breast cancer; Cellular uptake; PROTEIN; PROLIFERATION; NANOCARRIERS; FORMULATION; EXPRESSION; MICRORNAS; MIGRATION; MIRNAS; CELLS;
D O I
10.1016/j.jsps.2021.04.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nowadays, microRNA is considered an attractive strategy for the effective treatment of cancer. A significant delivery of microRNA for cancer therapy remains a significant obstacle to target cancer cells. The restoring microRNA-1296 (miR-1296) has immense therapeutic efficacy in triple-negative breast cancer (TNBC). TNBC is an aggressive subtype of breast tumors with the progression of malignant transformation. This study aimed to develop a cationic nanoliposome that can serve as a miR-1296 carrier and studied its efficiency in TNBC. The efficacy of miR-1296 liposomes was evaluated on its apoptotic effect, cellular uptake, and potential chemotherapy sensitization in the TNBC cell line (MDA-MB-231). For in vitro viability study, the apoptotic effect was performed to validate protein expression using Alamar blue kit and western blot. The transfection of miR-1296 into TNBC cells was also investigated using cisplatin as a TNBC resistance drug. The fluorescent miR-1296-cy3 liposome was used for cellular uptake study. The miR-liposome was successfully prepared with a particle size of 123.6 +/- 1.3 nm and encapsulation efficiency of 94.33%. A dose of 0.5 uM has significantly reduced the viability of MDA-MB-231 to be 33.45%+/- 5.29 (P < 0.001). This result was validated by down-expression of CCND1, and PARP1, the miR1296 receptor, and apoptosis marker. The image of the miR-1296-cy3 liposome showed cytoplasmic intracellular localization. It was found high sensitization of TNBC cell line for miR-1296 liposome compared to cisplatin (P < 0.001). Future in vivo research may answer questions concerning safety and stability. This study demonstrates that miR-191 liposomes may have promising clinical applications for TNBC therapy. (c) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:446 / 455
页数:10
相关论文
共 35 条
[1]   ynthesis, characterization, and evaluation of poly (D, L-lactide-co-glycolide)-based nanoformulation of miRNA-150: potential implications for pancreatic cancer therapy [J].
Arora, Sumit ;
Swaminathan, Suresh K. ;
Kirtane, Ameya ;
Srivastava, Sanjeev K. ;
Bhardwaj, Arun ;
Singh, Seema ;
Panyam, Jayanth ;
Singh, Ajay P. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2014, 9 :2933-2942
[2]  
Ballinger T., 2016, TRIPLE NEGATIVE BREA
[3]   Tumor suppressor role of microRNA-1296 in triple-negative breast cancer [J].
Binh Phan ;
Majid, Shahana ;
Ursu, Sarah ;
de Semir, David ;
Nosrati, Mehdi ;
Bezrookove, Vladimir ;
Kashani-Sabet, Mohammed ;
Dar, Altaf A. .
ONCOTARGET, 2016, 7 (15) :19519-19530
[4]  
Cappione A., 2012, INT J PROTEOMICS
[5]   miR-1296-5p decreases ERBB2 expression to inhibit the cell proliferation in ERBB2-positive breast cancer [J].
Chen, Gang ;
He, Mingfeng ;
Yin, Yin ;
Yan, Ting ;
Cheng, Wenfang ;
Huang, Zebo ;
Zhang, Lan ;
Zhang, Huo ;
Liu, Ping ;
Zhu, Wei ;
Zhu, Yichao .
CANCER CELL INTERNATIONAL, 2017, 17
[6]   In vivo delivery of miRNAs for cancer therapy: Challenges and strategies [J].
Chen, Yunching ;
Gao, Dong-Yu ;
Huang, Leaf .
ADVANCED DRUG DELIVERY REVIEWS, 2015, 81 :128-141
[7]   MicroRNAs and Triple Negative Breast Cancer [J].
D'Ippolito, Elvira ;
Iorio, Marilena V. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (11) :22202-22220
[8]   SYNTHESIS OF CONGENERS AND PRODRUGS .3. WATER-SOLUBLE PRODRUGS OF TAXOL WITH POTENT ANTITUMOR-ACTIVITY [J].
DEUTSCH, HM ;
GLINSKI, JA ;
HERNANDEZ, M ;
HAUGWITZ, RD ;
NARAYANAN, VL ;
SUFFNESS, M ;
ZALKOW, LH .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (04) :788-792
[9]  
Eades G., 2014, MOL CANC RES MOLCANR
[10]   Targeting microRNAs in cancer: rationale, strategies and challenges [J].
Garzon, Ramiro ;
Marcucci, Guido ;
Croce, Carlo M. .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (10) :775-789