Abstract
Background: Tumor metastasis is a main cause of death in patients with breast cancer.
The cross-talk between cancer-associated fibroblasts (CAFs) and tumor cells plays an important
role in promoting tumor invasion and metastasis. It is important to develop a novel delivery system
to inhibit tumor development by simultaneously targeting both CAFs and tumor cells.
Objectives: The main objective of this research was to prepare nanoparticles to inhibit tumor
proliferation and migration by blocking the cross-talk of tumor-CAFs. Additionally, a novel “MCF-
7+NIH/3T3” mixed cell model was established to mimic the tumor microenvironment (TME).
Methods: In this study, the pH-responsive nanoparticles (MIF/DOX-sul-HA NPs) based on sulfated
hyaluronic acid (sul-HA) polymers were prepared for co-delivery of doxorubicin (DOX) and
mifepristone (MIF). The effects of anti-proliferation and anti-metastasis of MIF/DOX-sul-HA NPs
were investigated both in vitro and in vivo.
Results: The results showed that MIF/DOX-sul-HA NPs were nearly spherical in shape with
narrow particle size distribution and pH-responsive drug release, and could be taken up by both
MCF-7 and NIH/3T3 cells. Compared with MCF-7 cells alone, the anti-tumor effect of single DOX
was weak in the “MCF-7+NIH/3T3” mixed cell model. MIF/DOX-sul-HA NPs exhibited strong
effects of anti-proliferation and anti-metastasis than the free single drug.
Conclusion: The sul-HA nanoparticles for co-delivery of DOX and MIF could be a promising
combined therapy strategy for the treatment of breast cancer.
Keywords:
Breast cancer, delivery, nanoparticles, combination, fibroblast, CAFs.
[18]
Zhang L, Zhang Y, Xue Y, et al. Transforming weakness into strength: Photothermal-therapy-induced inflammation enhanced cytopharmaceutical chemotherapy as a combination anticancer treatment. Adv Mater 2019; 31: e1805936.
[20]
Huang L, Li J. Liposomes comprising a calcium phosphatecontaining precipitate. US Patent 201815948202, 2018.
[21]
Barenholz Y, Cohen R. Composition of matter comprising liposomes embedded in a polymeric matrix and methods of using same. US Patent 201916254084, 2019.
[22]
Hong K, Drummond D, Kirpotin D. Liposomes useful for drug delivery. US Patent 201815896389, 2018.
[23]
Guo X, Wang L, Duval K, Fan J, Zhou S, Chen Z. Dimeric drug polymeric micelles with acid-active tumor targeting and FRET-traceable drug release. Adv Mater 2018; 30(3): 201705436.
[24]
Immunogen I. Targeted delivery of cyclopropylbenzindolecontaining cytotoxic drugs. US Patent 46830695, 1995.
[25]
Ekwuribe NN, Price CH, Ansari AM, et al. Mixtures of growth hormone drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same. US Patent 87375701, 2001.
[27]
Jacquinot E, Perard M, Falk U. Process for the preparation of aqueous suspensions of anionic colloidal silica having a neutral pH and applications thereof. US Patent 87273807, 2007.
[28]
Canova Levy A. Silica filler for epoxy encapsulants and epoxy encapsulants containing same. US Patent 78102585, 1988.
[30]
Ghiani S, Maiocchi A, Caminiti L. Fluorescent solid lipid nanoparticles composition and preparation thereof. US Patent 16263769, 2019.
[31]
Brioschi C, Cabella C, Ghiani S. Paramagnetic solid lipid nanoparticles (pSLNs) containing metal amphiphilic complexes for MRI. EP Patent 068463, 2013.
[37]
Wu JL, Jiang H, Gao AQ, et al. A preparation method and application of liver-targeting polymer, liver-targeting liposome. CN Patent 109364024A, 2019.