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Published on: September 19, 2018
Targeting epidermal growth factor receptors and downstream signaling pathways in cancer by phytochemicals
Onat Kadioglu1, Jingming Cao, Mohamed E M Saeed
1Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Mainz, Germany.
Abstract:
Epidermal growth factor receptors (EGFR, HER2, HER3) activate signal transduction pathways involved in cancer proliferation, apoptosis, differentiation, metastasis, and angiogenesis. Their overexpression and activation are associated with unfavorable prognosis of cancer patients. Therefore, they are attractive targets for cancer therapy. Due to the development of drug resistance, therapeutic monoclonal antibodies and synthetic small molecule tyrosine kinase inhibitors directed against EGFR family members may fail with fatal consequences for cancer patients. Medicinal plants raised considerable interest during the past years as valuable resources to develop novel treatment therapies targeting epidermal growth factor receptors and their downstream signal transduction pathways. The present review gives an overview of isolated phytochemicals that inhibit these signaling routes. Inhibitors have been described that down-regulate the mRNA or protein expression of EGFR, HER2, or HER3 or inhibit the phosphorylation of these receptors and/or their downstream signaling kinases. Remarkably, a wealth of in vivo experiments complemented in vitro data, indicating that natural products are also active in living animals bringing this research concept closer to clinical applicability. The combination of receptor-inhibiting natural product with standard anticancer drugs frequently caused increased or even synergistic tumor inhibition in vitro and in vivo. It deserves further evaluation, if and how epidermal growth factor receptor-targeting natural products can be integrated into clinical oncology as well as to define their role for more tumor-specific and individualized tumor therapies.
Insights
Medicinal plants offer novel cancer therapies by inhibiting epidermal growth factor receptors (EGFR, HER2, HER3) and their signaling pathways. These natural compounds show promise in preclinical studies, including synergistic effects with conventional drugs.
Area of Science:
- Oncology
- Pharmacology
- Natural Product Chemistry
Background:
- Epidermal growth factor receptors (EGFR, HER2, HER3) are crucial in cancer development and are key therapeutic targets.
- Drug resistance to existing EGFR-family inhibitors necessitates the exploration of alternative therapeutic strategies.
- Medicinal plants are recognized as a rich source for novel anticancer agents.
Purpose of the Study:
- To review phytochemicals isolated from medicinal plants that inhibit EGFR, HER2, and HER3 signaling pathways.
- To assess the potential of these natural compounds as anticancer therapeutics.
- To explore the clinical applicability and combination strategies of natural EGFR inhibitors.
Main Methods:
- Literature review of studies reporting phytochemicals targeting EGFR family signaling.
- Analysis of in vitro and in vivo experimental data on isolated inhibitors.
- Evaluation of combination therapies involving natural products and standard anticancer drugs.
Main Results:
- Numerous phytochemicals identified that down-regulate EGFR, HER2, or HER3 expression or inhibit their phosphorylation.
- In vitro and in vivo studies demonstrate the efficacy of these natural inhibitors in preclinical cancer models.
- Combination of natural EGFR inhibitors with conventional drugs often leads to enhanced or synergistic tumor inhibition.
Conclusions:
- Phytochemicals represent a promising avenue for developing novel therapies against EGFR-driven cancers, overcoming drug resistance.
- In vivo activity of natural products supports their clinical relevance and potential integration into oncology.
- Further research is warranted to define the role of natural EGFR inhibitors in personalized and combination cancer therapies.
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