NF kappa B mediates cisplatin resistance through histone modifications in head and neck squamous cell carcinoma (HNSCC)

作者：Almeida Luciana O; Abrahao Aline C; Rosselli Murai Luciana K; Giudice Fernanda S; Zagni Chiara; Leopoldino Andreia M; Squarize Cristiane H; Castilho Rogerio M^*

来源：FEBS Open Bio, 2014, 4(1): 96-104.

DOI：10.1016/j.fob.2013.12.003

• HNSCC
• Chromatin remodeling
• HDAC inhibitor
• Histone acetylation
• NF kappa B
• Chemoresistance

Cisplatin-based chemotherapy is the standard treatment of choice for head and neck squamous cell carcinoma (HNSCC). The efficiency of platinum-based therapies is directly influenced by the development of tumor resistance. Multiple signaling pathways have been linked to tumor resistance, including activation of nuclear factor kappa B (NF kappa B). We explore a novel mechanism by which NF kappa B drives HNSCC resistance through histone modifications. Post-translational modification of histones alters chromatin structure, facilitating the binding of nuclear factors that mediate DNA repair, transcription, and other processes. We found that chemoresistant HNSCC cells with active NF kappa B signaling respond to chemotherapy by reducing nuclear BRCA1 levels and by promoting histone deacetylation (chromatin compaction). Activation of this molecular signature resulted in impaired DNA damage repair, prolonged accumulation of histone gamma H2AX and increased genomic instability. We found that pharmacological induction of histone acetylation using HDAC inhibitors prevented NF kappa B-induced cisplatin resistance. Furthermore, silencing NF kappa B in HNSCC induced acetylation of tumor histones, resulting in reduced chemoresistance and increased cytotoxicity following cisplatin treatment. Collectively, these findings suggest that epigenetic modifications of HNSCC resulting from NF kappa B-induced histone modifications constitute a novel molecular mechanism responsible for chemoresistance in HNSCC. Therefore, targeted inhibition of HDAC may be used as a viable therapeutic strategy for disrupting tumor resistance caused by NF kappa B.

• 出版日期2014