Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer

Abstract Targeted delivery of drugs to tumor cells, which circumvent resistance mechanisms and induce cell killing, is a lingering challenge that requires innovative solutions. Here, we provide two bioengineered strategies in which nanotechnology is blended with cancer medicine to preferentially target distinct mechanisms of drug resistance. In the first ‘case study’, we demonstrate the use of lipid–drug conjugates that target molecular signaling pathways, which result from taxane-induced drug tolerance via cell surface lipid raft accumulations. Through a small molecule drug screen, we identify a kinase inhibitor that optimally destroys drug tolerant cancer cells and conjugate it to a rationally-chosen lipid scaffold, which enhances anticancer efficacy in vitro and in vivo. In the second ‘case study’, we address resistance mechanisms that can occur through exocytosis of nanomedicines. Using adenocarcinoma HeLa and MCF-7 cells, we describe the use of gold nanorod and nanoporous vehicles integrated with an optical antenna for on-demand, photoactivation at ∼650 nm enabling release of payloads into cells including cytotoxic anthracyclines. Together, these provide two approaches, which exploit engineering strategies capable of circumventing distinct resistance barriers and induce killing by multimodal, including nanophotonic mechanisms.

[1]  Nicholas A. Peppas,et al.  Engineering precision nanoparticles for drug delivery , 2020, Nature reviews. Drug discovery.

[2]  A. Goldman,et al.  Engineering in Medicine To Address the Challenge of Cancer Drug Resistance: From Micro- and Nanotechnologies to Computational and Mathematical Modeling. , 2020, Chemical reviews.

[3]  Zheng-chao Tu,et al.  GZD824 as a FLT3, FGFR1 and PDGFRα Inhibitor Against Leukemia In Vitro and In Vivo , 2020, Translational oncology.

[4]  Anirudhan T S,et al.  Effect of dual stimuli responsive dextran/nanocellulose polyelectrolyte complexes for chemophotothermal synergistic cancer therapy. , 2019, International journal of biological macromolecules.

[5]  Da In Kim,et al.  Gold Nanocage-Incorporated Poly(ε-Caprolactone) (PCL) Fibers for Chemophotothermal Synergistic Cancer Therapy , 2019, Pharmaceutics.

[6]  V. Schirrmacher From chemotherapy to biological therapy: A review of novel concepts to reduce the side effects of systemic cancer treatment (Review) , 2018, International journal of oncology.

[7]  Angus P R Johnston,et al.  The Endosomal Escape of Nanoparticles: Toward More Efficient Cellular Delivery. , 2018, Bioconjugate chemistry.

[8]  Leonardo Fernandes Fraceto,et al.  Nano based drug delivery systems: recent developments and future prospects , 2018, Journal of Nanobiotechnology.

[9]  Dawei Gao,et al.  Multistimuli-responsive drug vehicles based on gold nanoflowers for chemophotothermal synergistic cancer therapy. , 2018, Nanomedicine.

[10]  M. Vallet‐Regí,et al.  Mesoporous Silica Nanoparticles for Drug Delivery: Current Insights , 2017, Molecules.

[11]  Xiaoyu Xu,et al.  Injectable, NIR/pH-Responsive Nanocomposite Hydrogel as Long-Acting Implant for Chemophotothermal Synergistic Cancer Therapy. , 2017, ACS applied materials & interfaces.

[12]  Yangqiu Li,et al.  GZD824 suppresses the growth of human B cell precursor acute lymphoblastic leukemia cells by inhibiting the SRC kinase and PI3K/AKT pathways , 2016, Oncotarget.

[13]  Ami Patel,et al.  Novel roles of Src in cancer cell epithelial-to-mesenchymal transition, vascular permeability, microinvasion and metastasis. , 2016, Life sciences.

[14]  A. Goldman Tailoring combinatorial cancer therapies to target the origins of adaptive resistance , 2016, Molecular & cellular oncology.

[15]  P. Majumder,et al.  Temporally sequenced anticancer drugs overcome adaptive resistance by targeting a vulnerable chemotherapy-induced phenotypic transition , 2015, Nature Communications.

[16]  Ji-Ho Park,et al.  Endocytosis and exocytosis of nanoparticles in mammalian cells , 2014, International journal of nanomedicine.

[17]  Si-Han Wu,et al.  Synthesis of mesoporous silica nanoparticles. , 2013, Chemical Society reviews.

[18]  Courtney R. Thomas,et al.  Involvement of lysosomal exocytosis in the excretion of mesoporous silica nanoparticles and enhancement of the drug delivery effect by exocytosis inhibition. , 2013, Small.

[19]  Luke P. Lee,et al.  Photonic gene circuits by optically addressable siRNA-Au nanoantennas. , 2012, ACS nano.

[20]  Michael M Gottesman,et al.  Collateral sensitivity as a strategy against cancer multidrug resistance. , 2012, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

[21]  Juan L. Vivero-Escoto,et al.  Exocytosis of mesoporous silica nanoparticles from mammalian cells: from asymmetric cell-to-cell transfer to protein harvesting. , 2011, Small.

[22]  M. Pegram,et al.  Triple negative breast cancer: unmet medical needs , 2011, Breast Cancer Research and Treatment.

[23]  Luke P. Lee,et al.  Biomolecular plasmonics for quantitative biology and nanomedicine. , 2010, Current opinion in biotechnology.

[24]  Samuel A Wickline,et al.  Exploiting lipid raft transport with membrane targeted nanoparticles: a strategy for cytosolic drug delivery. , 2008, Biomaterials.

[25]  A. Ostafin,et al.  Synthesis of nanoscale mesoporous silica spheres with controlled particle size , 2002 .

[26]  C. Redmond,et al.  Doxorubicin-containing regimens for the treatment of stage II breast cancer: The National Surgical Adjuvant Breast and Bowel Project experience. , 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[27]  Baolin Zhang,et al.  Drug-biomarker co-development in oncology - 20 years and counting. , 2017, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

[28]  W. S. Vanden Berg-Foels,et al.  Bioengineering strategies for designing targeted cancer therapies. , 2013, Advances in cancer research.

[29]  F. Lombardo,et al.  Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. , 2001, Advanced drug delivery reviews.