Affiliation:
1. The University of Kansas Medical
Center, Cancer Biology, Kansas City, KS 66160, USA
2. Kansas State University, Department of Chemistry, Manhattan, KS 66506, USA
Abstract
Abstract:
Mitochondria are important intracellular organelles because of their key roles in cellular metabolism,
proliferation, and programmed cell death. The differences in the structure and function of the
mitochondria of healthy and cancerous cells have made mitochondria an interesting target for drug delivery.
Mitochondrial targeting is an emerging field as the targeted delivery of cytotoxic payloads and
antioxidants to the mitochondrial DNA is capable of overcoming multidrug resistance. Mitochondrial
targeting is preferred over nuclear targeting because it can take advantage of the distorted metabolism
in cancer. The negative membrane potential of the inner and outer mitochondrial membranes, as well as
their lipophilicity, are known to be the features that drive the entry of compatible targeting moiety,
along with anticancer drug conjugates, towards mitochondria. The design of such drug nanocarrier conjugates
is challenging because they need not only to target the specific tumor/cancer site but have to
overcome multiple barriers as well, such as the cell membrane and mitochondrial membrane. This review
focuses on the use of peptide-based nanocarriers (organic nanostructures such as liposomes, inorganic,
carbon-based, and polymers) for mitochondrial targeting of the tumor/cancer. Both in
vitro and in vivo key results are reported.
Funder
National Science Foundation, USA
Publisher
Bentham Science Publishers Ltd.
Subject
Cell Biology,Molecular Biology,Biochemistry,General Medicine
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献