Butyrate response factor 1 enhances cisplatin sensitivity in human head and neck squamous cell carcinoma cell lines. Academic Article uri icon

Overview

abstract

  • Cisplatin is a widely used chemotherapeutic agent in head and neck squamous cell carcinoma (HNSCC). Resistance to cisplatin is a common feature of HNSCC. To identify genes that may regulate cisplatin sensitivity, we carried out a cDNA microarray analysis of gene expression in cisplatin-sensitive and cisplatin-resistant HNSCC-derived cell lines. Among genes differentially expressed by cisplatin treatment, we have confirmed the elevated expression of butyrate responsive factor 1 (BRF1) in cisplatin-sensitive HNSCC cells and have demonstrated that the expression level of BRF1 is associated with cisplatin-sensitivity. Specific inhibition of BRF1 expression using an antisense oligodeoxynucleotide (ODN) decreased the cisplatin-sensitivity and, on the contrary, overexpression of BRF1 increased cisplatin-sensitivity in HNSCC cells. Elevated expression of BRF1 decreased the level of the human inhibitor of apoptosis protein-2 (cIAP2) and increased the caspase-3 activity in HNSCC cells. In addition, elevated expression of BRF1 decreased the expression level of enhanced green fluorescent protein (EGFP) linked to a 3' terminal AU-rich element (ARE) of cIAP2 mRNA. These findings demonstrate that BRF1 expression enhanced cisplatin sensitivity in HNSCC cells by reducing the levels of cIAP2 mRNA.

authors

  • Lee, Seung Koo
  • Kim, Seong Bum
  • Kim, Jong Soo
  • Moon, Chang Hoon
  • Han, Myung Shin
  • Lee, Byung Ju
  • Chung, Dae Kyun
  • Min, Young Joo
  • Park, Jae Hoo
  • Choi, Dae Hwa
  • Cho, Hong Rae
  • Park, Sang Kyu
  • Park, Jeong Woo

publication date

  • October 20, 2005

Research

keywords

  • Antineoplastic Agents
  • Carcinoma, Squamous Cell
  • Cisplatin
  • DNA-Binding Proteins
  • Head and Neck Neoplasms
  • Immediate-Early Proteins

Identity

Scopus Document Identifier

  • 24344502263

Digital Object Identifier (DOI)

  • 10.1002/ijc.21133

PubMed ID

  • 15880358

Additional Document Info

volume

  • 117

issue

  • 1