Abstract

Head and neck cancers, which affect 650,000 people and cause 350,000 deaths per year, is the sixth leading cancer by cancer incidence and eighth by cancer-related death worldwide. Oral cancer is the most common type of head and neck cancer. More than 90% of oral cancers are oral and oropharyngeal squamous cell carcinoma (OSCC). The overall five-year survival rate of OSCC patients is approximately 63%, which is due to the low response rate to current therapeutic drugs. In this review we discuss the possibility of using caffeic acid phenethyl ester (CAPE) as an alternative treatment for oral cancer. CAPE is a strong antioxidant extracted from honeybee hive propolis. Recent studies indicate that CAPE treatment can effectively suppress the proliferation, survival, and metastasis of oral cancer cells. CAPE treatment inhibits Akt signaling, cell cycle regulatory proteins, NF-κB function, as well as activity of matrix metalloproteinase (MMPs), epidermal growth factor receptor (EGFR), and Cyclooxygenase-2 (COX-2). Therefore, CAPE treatment induces cell cycle arrest and apoptosis in oral cancer cells. According to the evidence that aberrations in the EGFR/phosphoinositide 3-kinase (PI3K)/protein kinase B (Akt) signaling, NF-κB function, COX-2 activity, and MMPs activity are frequently found in oral cancers, and that the phosphorylation of Akt, EGFR, and COX-2 correlates to oral cancer patient survival and clinical progression, we believe that CAPE treatment will be useful for treatment of advanced oral cancer patients.

Highlights

  • Head and neck cancers include cancers evolved from the oral cavity, pharynx, larynx, paranasal sinuses and nasal cavity, and salivary glands

  • According to the facts that caffeic acid phenethyl ester (CAPE) treatment is able to inhibit the activity and abundance of epidermal growth factor receptor (EGFR) and COX-2, we believe that administration of CAPE can prevent and delay the development or progression of oral cancers

  • The oral epidermoid carcinoma-Meng 1 (OEC-M1) cell line is a human oral epidermoid carcinoma generated from the primary lesion of an oral carcinoma in a Taiwanese patient, which is a p53 mutant, resistant to retinoic acid treatment, and expresses smaller sized hypophosphorylated Rb proteins compared with normal cells [45,92]

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Summary

Introduction

Head and neck cancers include cancers evolved from the oral cavity, pharynx, larynx, paranasal sinuses and nasal cavity, and salivary glands. Oral cancer is the most common type of head and neck cancer and caused 135,000 deaths worldwide in 2013 [3]. Several recent studies indicate that CAPE treatment suppresses proliferation, survival, and invasion of human oral cancer cells. We discuss the potential of using CAPE as a treatment for patients with oral cancer in this review article

Oral Cancer
Chemoprevention Effects of CAPE on Oral Cancer Cells
Anticancer Activity Effects of CAPE on Oral Cancer Cells
Molecular Mechanism of Anticancer Activity of CAPE in Oral Cancer Cells
Conclusions
Findings
Conflicts of Interest
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