Komatsu Naoki, Kawamata Norihiko, Takeuchi Seisho, Yin Dong, Chien Wenwen, Miller Carl W, Koeffler H Phillip
Department of Hematology/Respiratory, Cedars-Sinai Medical Center/University of California at Los Angeles School of Medicine, 90048, USA.
Oncol Rep. 2006 Jan;15(1):187-91.
Current chemotherapy of advanced non-small cell lung cancer (NSCLC) produces only a modest increase in survival time. New approaches are needed for this disease. The development of lung cancer is associated with silencing tumor suppressor genes that can occur not only by deletion or mutation, but also by epigenetic changes including histone deacetylation of key lysines. Histone deacetylase inhibitor (HDACI) increases histone acetylation, resulting in DNA with a more open chromatin that favors transcription. We found that the HDACI, suberoylanilide hydroxamic acid (SAHA), suppressed cell growth of five non-small cell lung cancer cell lines in a dose-dependent manner (50% growth inhibition approximately 2 microM). Cell cycle assay by fluorescence-activated cell sorting (FACS) demonstrated that SAHA induced a significant G0-G1 growth arrest of NSCLC cells. Protein assay by Western blot analysis showed that SAHA induced expression of p21WAF1. These results demonstrated that administration of SAHA may be a novel approach to the treatment of non-small cell lung cancer.
目前晚期非小细胞肺癌(NSCLC)的化疗仅使生存时间略有延长。针对这种疾病需要新的治疗方法。肺癌的发生与肿瘤抑制基因沉默有关,这种沉默不仅可通过缺失或突变发生,还可通过表观遗传变化发生,包括关键赖氨酸的组蛋白去乙酰化。组蛋白去乙酰化酶抑制剂(HDACI)可增加组蛋白乙酰化,导致染色质更开放的DNA,有利于转录。我们发现,HDACI 辛二酰苯胺异羟肟酸(SAHA)以剂量依赖方式抑制五种非小细胞肺癌细胞系的细胞生长(约2 microM时50%生长抑制)。通过荧光激活细胞分选(FACS)进行的细胞周期分析表明,SAHA诱导NSCLC细胞显著的G0-G1期生长停滞。通过蛋白质印迹分析进行的蛋白质检测表明,SAHA诱导p21WAF1表达。这些结果表明,给予SAHA可能是治疗非小细胞肺癌的一种新方法。