Abstract

Transient chemotherapeutic response is a major obstacle to treating head and neck squamous cell carcinomas (HNSCC). Histone methyltransferase G9a has recently been shown to be abundantly expressed in HNSCC, and is required to maintain the malignant phenotype. In this study, we found that high G9a expression is significantly associated with poor chemotherapeutic response and disease-free survival in HNSCC patients. Similarly, G9a expression and enzymatic activity were elevated in cisplatin-resistant HNSCC cells. Genetic or pharmacologic inhibition of G9a sensitized the resistant cells to cisplatin, increasing cellular apoptosis. Mechanistic investigations indicated that G9a contributes to transcriptional activation of the glutamate-cysteine ligase catalytic subunit (GCLC), which results in upregulation of cellular glutathione (GSH) and drug resistance. In addition, we observed a significant positive correlation between G9a and GCLC expression in tumors of HNSCC patients. Taken together, our findings provide evidence that G9a protects HNSCC cells against chemotherapy by increasing the synthesis of GSH, and imply G9a as a promising target for overcoming cisplatin resistance in HNSCC. Mol Cancer Ther; 16(7); 1421-34. ©2017 AACR.

Highlights

  • Head and neck squamous cell carcinoma (HNSCC) is the sixth leading cause of cancer-related deaths worldwide, and has become a major public health problem owing to its serious impact on patients' quality of life [1]

  • G9a expression is associated with poor chemotherapeutic response and cisplatin sensitivity in HNSCC

  • To investigate the effect of G9a expression on chemotherapeutic response in HNSCC, 56 surgical resection tumor specimens from HNSCC patients receiving neoadjuvant therapy were subjected to IHC analysis with a G9a-specific antibody

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Summary

Introduction

Head and neck squamous cell carcinoma (HNSCC) is the sixth leading cause of cancer-related deaths worldwide, and has become a major public health problem owing to its serious impact on patients' quality of life [1]. Despite decades of improving treatment strategies, the prognosis for advanced HNSCC remains unfavorable. One of the main obstacles to successful HNSCC treatment is acquired resistance to anticancer drugs. The response rate to most first-line chemotherapy regimens decreases [2]. It is urgent to elucidate the mechanisms causing HNSCC unresponsiveness to anticancer drugs. Emerging evidence indicates that alteration of epigenetics could lead to acquired drug resistance [3].

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