Cisplatin plus cetuximab inhibits cisplatin‐resistant human oral squamous cell carcinoma cell migration and proliferation but does not enhance apoptosis

Abstract

Cisplatin is among the most widely used anticancer drugs used in the treatment of several malignancies, including oral cancer. However, cisplatin treatment often promotes chemical re-sistance, subsequently causing treatment failure. Several studies have shown that epidermal growth factor receptors (EGFRs) play a variety of roles in cancer progression and overcoming cisplatin re-sistance. Therefore, this study focused on EGFR inhibitors used in novel targeted therapies as a method to overcome this resistance. We herein aimed to determine whether the combined effects of cisplatin and cetuximab could enhance cisplatin sensitivity by inhibiting the epithelial‐to‐mesen-chymal transition (EMT) process in cisplatin‐resistant cells. In vitro analyses of three cisplatin‐re-sistant oral squamous cell carcinoma cells, which included cell proliferation assay, combination in-dex calculation, cell cytotoxicity assay, live/dead cell count assay, Western blot assay, propidium iodide staining assay, scratch assay, and qRT‐PCR assay were then conducted. Our results showed that a cisplatin/cetuximab combination treatment inhibited cell proliferation, cell motility, and N‐ cadherin protein expression but induced E‐cadherin and claudin‐1 protein expression. Although the combination of cisplatin and cetuximab did not induce apoptosis of cisplatin‐resistant cells, it may be useful in treating oral cancer patients with cisplatin resistance given that it controls cell motility and EMT‐related proteins.