基因
基因表达
细胞培养
分子生物学
细胞周期
生物
增强子
黑色素瘤
DNA微阵列
遗传学
作者
Yoshitaka Matsumoto,Mayumi Iwakawa,Yoshiya Furusawa,Ken-Ichi Ishikawa,Mizuho Aoki,Kaori Imadome,Izumi Matsumoto,Hirohiko Tsujii,Koichi Andō,Takashi Imai
标识
DOI:10.1080/09553000801953334
摘要
To elucidate the molecular changes in response to carbon beams (C-ions) in melanoma.We examined expression profiles of 6 melanoma cell lines exposed to C-ions or X-rays with 2 Gy using single-color microarrays.Twenty-two genes, including nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (NFKBIA), responded to C-ions in all six cell lines, based on analysis of variance (ANOVA) filtering (p < 0.001). We found 173 genes that responded in common to C-ions in four cell lines. We identified many down-regulated genes including the cell cycle - related genes that were more responsive to C-ions than X-rays. In contrast, most of the up-regulated genes including the tumor protein p53 (p53) target genes responded to both C-ions and X-rays. C-ions induced G2/M arrest significantly more than X-rays at 30 h (p < 0.05).Our findings suggest that down-regulation of gene expression plays a key role in the response to C-ions. Regulation of cell cycle - related genes and induction of prolonged G2/M arrest may be responsible for the extra sensitivity to C-ions, whereas p53-related genes may have similar roles in the sensitivities to both C-ions and X-rays.
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