Enhancing Anti-Tumor Activity of Sorafenib Mesoporous Silica Nanomatrix in Metastatic Breast Tumor and Hepatocellular Carcinoma via the Co-Administration with Flufenamic Acid

Autor: Yang Guo, Shuang Zhang, Jing-Ru Wang, Mei-Qi Xu, Xiao-Chuan Duan, Man Liu, Xuan Zhang, Hui Li, Zhuo-Yue Li, Ai Liao, Zhen-Han Feng, Yi-Fan Yin, Shuai-Qiang Zhang, Guang-Xue Wang, Shu-Min Wang
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Male
Cell
Pharmaceutical Science
02 engineering and technology
01 natural sciences
Cell Movement
International Journal of Nanomedicine
Antineoplastic Combined Chemotherapy Protocols
sorafenib mesoporous silica nanomatrix
Drug Discovery
Original Research
Mice
Inbred BALB C

Chemistry
4T1/luc
Anti-Inflammatory Agents
Non-Steroidal

Liver Neoplasms
AKR1C1
Cell migration
Hep G2 Cells
General Medicine
Sorafenib
AKR1C3
Silicon Dioxide
021001 nanoscience & nanotechnology
medicine.anatomical_structure
Hepatocellular carcinoma
Female
lipids (amino acids
peptides
and proteins)

PGE2
medicine.symptom
0210 nano-technology
hormones
hormone substitutes
and hormone antagonists

medicine.drug
HepG2
Carcinoma
Hepatocellular

Biophysics
Mice
Nude

Breast Neoplasms
Bioengineering
Inflammation
010402 general chemistry
Dinoprostone
MSNM@SFN
Biomaterials
flufenamic acid
In vivo
Cell Line
Tumor

medicine
Animals
Humans
20-Hydroxysteroid Dehydrogenases
Organic Chemistry
Aldo-Keto Reductase Family 1 Member C3
medicine.disease
Xenograft Model Antitumor Assays
digestive system diseases
In vitro
Nanostructures
0104 chemical sciences
body regions
Flufenamic acid
Cancer research
FFA
Zdroj: International Journal of Nanomedicine
ISSN: 1178-2013
Popis: Zhuo-Yue Li,1,2 Yi-Fan Yin,1,2 Yang Guo,1,2 Hui Li,1,2 Mei-Qi Xu,1,2 Man Liu,1,2 Jing-Ru Wang,1,2 Zhen-Han Feng,1,2 Xiao-Chuan Duan,1,2 Shuang Zhang,1,2 Shuai-Qiang Zhang,1,2 Guang-Xue Wang,2 Ai Liao,2 Shu-Min Wang,3 Xuan Zhang1,2 1Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University, Beijing 100191, People’s Republic of China; 2Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing 100191, People’s Republic of China; 3Department of Ultrasound, Peking University Third Hospital, Peking University, Beijing 100191, People’s Republic of ChinaCorrespondence: Xuan ZhangDepartment of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Xueyuan Road 38, Beijing 100191, People’s Republic of ChinaTel/Fax +86-10-82805765Email xuanzhang@bjmu.edu.cnShu-Min WangDepartment of Ultrasound, Peking University Third Hospital, Peking University, Xueyuan Road 38, Beijing 100191, People’s Republic of ChinaEmail shuminwang2014@163.comIntroduction: Because tumor-associated inflammation is a hallmark of cancer treatment, in the present study, sorafenib mesoporous silica nanomatrix (MSNM@SFN) co-administrated with flufenamic acid (FFA, a non-steroidal anti–inflammatory drug (NSAID)) was investigated to enhance the anti-tumor activity of MSNM@SFN.Methods: Metastatic breast tumor 4T1/luc cells and hepatocellular carcinoma HepG2 cells were selected as cell models. The effects of FFA in vitro on cell migration, PGE2 secretion, and AKR1C1 and AKR1C3 levels in 4T1/luc and HepG2 cells were investigated. The in vivo anti-tumor activity of MSNM@SFN co-administrating with FFA (MSNM@SFN+FFA) was evaluated in a 4T1/luc metastatic tumor model, HepG2 tumor-bearing nude mice model, and HepG2 orthotopic tumor-bearing nude mice model, respectively.Results: The results indicated that FFA could markedly decrease cell migration, PGE2 secretion, and AKR1C1 and AKR1C3 levels in both 4T1/luc and HepG2 cells. The enhanced anti-tumor activity of MSNM@SFN+FFA compared with that of MSNM@SFN was confirmed in the 4T1/luc metastatic tumor model, HepG2 tumor-bearing nude mice model, and HepG2 orthotopic tumor-bearing nude mice model in vivo, respectively.Discussion: MSNM@SFN co-administrating with FFA (MSNM@SFN+FFA) developed in this study is an alternative strategy for improving the therapeutic efficacy of MSNM@SFN via co-administration with NSAIDs.Keywords: sorafenib mesoporous silica nanomatrix, MSNM@SFN, flufenamic acid, FFA, PGE2, AKR1C1, AKR1C3, 4T1/luc, HepG2
Databáze: OpenAIRE