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Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer.
Saha, Tanmoy; Mondal, Jayanta; Khiste, Sachin; Lusic, Hrvoje; Hu, Zhang-Wei; Jayabalan, Ruparoshni; Hodgetts, Kevin J; Jang, HaeLin; Sengupta, Shiladitya; Eunice Lee, Somin; Park, Younggeun; Lee, Luke P; Goldman, Aaron.
Afiliação
  • Saha T; Division of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Mondal J; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Khiste S; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Lusic H; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Hu ZW; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Jayabalan R; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Hodgetts KJ; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Jang H; Division of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Sengupta S; Division of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Eunice Lee S; Department of Electrical & Computer Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
  • Park Y; Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
  • Lee LP; Division of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Goldman A; Division of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Nanophotonics ; 10(12): 3063-3073, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34589378
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article