TY - JOUR
T1 - Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer
AU - Saha, Tanmoy
AU - Mondal, Jayanta
AU - Khiste, Sachin
AU - Lusic, Hrvoje
AU - Hu, Zhang Wei
AU - Jayabalan, Ruparoshni
AU - Hodgetts, Kevin J.
AU - Jang, Haelin
AU - Sengupta, Shiladitya
AU - Lee, Somin Eunice
AU - Park, Younggeun
AU - Lee, Luke P.
AU - Goldman, Aaron
N1 - Publisher Copyright:
© 2021 Tanmoy Saha et al., published by De Gruyter, Berlin/Boston.
PY - 2021/9/2
Y1 - 2021/9/2
N2 - 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.
AB - 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.
KW - cancer biology
KW - chemotherapy
KW - drug resistance
KW - nanomedicine
UR - https://www.scopus.com/pages/publications/85109013373
U2 - 10.1515/nanoph-2021-0142
DO - 10.1515/nanoph-2021-0142
M3 - Article
AN - SCOPUS:85109013373
SN - 2192-8614
VL - 10
SP - 3063
EP - 3073
JO - Nanophotonics
JF - Nanophotonics
IS - 12
ER -