Targeting TME with nanocarriers (NCs) has been widely used to directly deliver anticancer drugs to control TME, which has revealed auspicious outcomes.
First-pass extracted concept
nanocarriers for tumor microenvironment-targeted cancer therapy
Aliases
nanocarriers, NCs
Evidence Snippets
Supporting Sources
Linked Claims
Nanocarriers have been widely used to directly deliver anticancer drugs to target and control the tumor microenvironment, with auspicious outcomes reported.
Nanocarriers can provide site-specific delivery, controlled release, enhanced solubility and stability, decreased toxicities, and improved pharmacokinetics and biodistribution.
Multiple nanocarrier classes, including metal nanocarriers, liposomal nanocarriers, solid lipid nanocarriers, micelles, nanoemulsions, polymer-based nanocarriers, dendrimers, nanoclays, and nanocrystals, have shown potential in preclinical studies by delivering anticancer drugs through distinct anticancer mechanisms.
Challenges in nanocarrier-mediated tumor microenvironment targeting include scale-up, rapid clearance by the mononuclear phagocyte system, and tumor microenvironment heterogeneity.
Nanocarriers can ameliorate the tumor microenvironment by regulating tumor-site redox environment, oxygen content, and pH.
Nanocarriers can reprogram the tumor microenvironment by regulating immunosuppressive factors and activating immunostimulatory cells.
Successful clinical translation of nanocarrier-based anticancer therapies requires careful study of drug loading optimization, nanocarrier-associated immunogenicity, and biocompatibility.
Some nanocarriers discussed for tumor microenvironment-targeted cancer therapy have already received US Food and Drug Administration approval, and some have entered clinical phases.