Abstract
Systemic administration of chemotherapeutics by nanocarriers (NCs) functionalized with targeting agents provides a localized accumulation of drugs in the target tissues and cells. Advanced nanoscaled medicaments can enter into the tumor microenvironment (TME) and overcome the uniquely dysregulated biological settings of TME, including highly pressurized tumor interstitial fluid in an acidic milieu. Such multimodal nanomedicines seem to be one of the most effective treatment modalities against solid tumors such as colorectal cancer (CRC). To progress and invade, cancer cells overexpress various oncogenes and molecular markers such as epidermal growth factor receptors (EGFRs), which can be exploited for targeted delivery of nanoscaled drug delivery systems (DDSs). In fact, to develop effective personalized multimodal nanomedicines, the type of solid tumor and status of the disease in each patient should be taken into consideration. While the development of such multimodal-targeted nanomedicines is largely dependent on the expression level of oncomarkers, the type of NCs and homing/imaging agents play key roles in terms of their efficient applications. In this review, we provide deep insights into the development of EGFR-targeting nanomedicines and discuss various types of nanoscale DDSs (e.g., organic and inorganic nanoparticles) for targeting of the EGFR-positive solid tumors such as CRC.
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Acknowledgements
This work is a part of a Ph.D. thesis supported (Grant No: 145/261) by the Research Center for Liver and gastrointestinal diseases, Tabriz University of Medical Sciences and Iran National Science Foundation (INSF) (Grant#: 96010102). The authors wish to acknowledge the technical support provided by the Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences. The kind help from Mrs. R Mousavi is highly appreciated.
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Akbarzadeh Khiavi, M., Safary, A., Barar, J. et al. Multifunctional nanomedicines for targeting epidermal growth factor receptor in colorectal cancer. Cell. Mol. Life Sci. 77, 997–1019 (2020). https://doi.org/10.1007/s00018-019-03305-z
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DOI: https://doi.org/10.1007/s00018-019-03305-z