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

Author:

Saha Tanmoy12,Mondal Jayanta2,Khiste Sachin2,Lusic Hrvoje2,Hu Zhang-Wei2,Jayabalan Ruparoshni2,Hodgetts Kevin J.2,Jang HaeLin12,Sengupta Shiladitya12,Lee Somin Eunice34,Park Younggeun5,Lee Luke P.12,Goldman Aaron126ORCID

Affiliation:

1. Division of Engineering in Medicine , Brigham and Women’s Hospital , Boston , MA , USA

2. Department of Medicine , Harvard Medical School , Boston , MA , USA

3. Department of Electrical & Computer Engineering , University of Michigan , Ann Arbor , MI 48109, USA

4. Department of Biomedical Engineering , Biointerfaces Institute, Applied Physics, Macromolecular Science and Engineering, University of Michigan , Ann Arbor , MI 48109, USA

5. Department of Mechanical Engineering , University of Michigan , Ann Arbor , MI 48109, USA

6. Cancer Immunology , Dana Farber/Harvard Cancer Center , Boston , MA , USA

Abstract

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.

Publisher

Walter de Gruyter GmbH

Subject

Electrical and Electronic Engineering,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials,Biotechnology

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