Abstract

Chemotherapy constitutes the standard modality of treatment for localized head and neck squamous cell carcinomas (HNSCC). However, many patients fail to respond and relapse after this treatments due to the acquisition of chemo-resistance. Therefore, there is an urgent need to develop novel drugs that could reverse the resistant phenotype. Curcumin, the constituent of the spice turmeric has been shown to have anti-inflammatory, anti-oxidant and anti-proliferative properties in several tumor types. However, use of curcumin has been limited due to its poor bio-absorption. Recently, a novel class of curcumin analogs, based on diarylidenylpiperidones (DAP), has been developed by incorporating a piperidone link to the beta-diketone structure and fluoro substitutions on the phenyl groups. In this study, we evaluated the effectiveness of H-4073, a parafluorinated variant of DAP, using both in vitro and in vivo head and neck cancer models. Our results demonstrate that H-4073 is a potent anti-tumor agent and it significantly inhibited cell proliferation in all the HNSCC cell lines tested in a dose-dependent manner. In addition, pretreatment of cisplatin-resistant HNSCC cell lines with H-4073 significantly reversed the chemo-resistance as observed by cell viability assay (MTT), apoptosis assay (Annexin V binding) and cleaved caspase-3 (Western blot). H-4073 mediated its anti-tumor effects by inhibiting JAK/STAT3, FAK, Akt and VEGF signaling pathways that play important roles in cell proliferation, migration, survival and angiogenesis. In the SCID mouse xenograft model, H-4073 significantly enhanced the anti-tumor and anti-angiogenesis effects of cisplatin, with no added systemic toxicity. Interestingly, H-4073 inhibited tumor angiogenesis by blocking VEGF production by tumor cells as well as directly inhibiting endothelial cell function. Taken together, our results suggest that H-4073 is a potent anti-tumor agent and it can be used to overcome chemotherapy resistance in HNSCC.

Highlights

  • Head and neck squamous cell carcinoma (HNSCC) is one of the most prevalent cancer worldwide with more than 600,000 cases are diagnosed every year [1]

  • CAL27-CisR was selected by growing the parental tongue squamous cell carcinoma cell line (CAL27) in increasing concentrations of cisplatin over an extended period of time [27]

  • Recent studies have shown that STAT3 is constitutively activated in tumor cells and is overexpressed in cisplatin-resistant cell lines [21,37]

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Summary

Introduction

Head and neck squamous cell carcinoma (HNSCC) is one of the most prevalent cancer worldwide with more than 600,000 cases are diagnosed every year [1]. It is being recognized that human papillomavirus (HPV) can play a role in the development of a subset of head and neck cancers [3]. Cisplatin is one of the commonly used chemotherapeutic agents for the treatment of head and neck cancers [5]. Cisplatin is an inorganic platinum agent, which can bind to DNA, inducing intrastrand and interstrand DNA crosslinks, as well as DNA-protein cross-links. These cross-links result in apoptosis and cell-growth inhibition [6]. There is a need to develop novel therapeutic strategies that are more effective and have fewer side effects than currently used treatment regimens

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