Multifunctional nanomedicines for targeting epidermal growth factor receptor in colorectal cancer.
Mostafa Akbarzadeh KhiaviAzam SafaryJaleh BararAmir AjoolabadyMohammad Hossein SomiYadollah OmidiPublished in: Cellular and molecular life sciences : CMLS (2019)
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.
Keyphrases
- epidermal growth factor receptor
- cancer therapy
- growth factor
- tyrosine kinase
- drug delivery
- small cell lung cancer
- pain management
- gene expression
- high resolution
- induced apoptosis
- chronic pain
- cell proliferation
- mass spectrometry
- oxidative stress
- signaling pathway
- binding protein
- drug release
- smoking cessation
- molecularly imprinted
- simultaneous determination