Chochi Yasuyo, Kawauchi Shigeto, Nakao Motonao, Furuya Tomoko, Hashimoto Kiichiro, Oga Atunori, Oka Masaaki, Sasaki Kohsuke
Department of Pathology, Yamaguchi University Graduate School of Medicine, Ube 755-8505, Japan.
J Pathol. 2009 Apr;217(5):677-84. doi: 10.1002/path.2491.
In accordance with cancer progression, genomic aberrations accumulate in cancer cells in a stepwise fashion. However, whether there are genomic changes linked with tumour progression remains unclarified. The purpose of this study is to elucidate the relationship between genomic alterations and clinical stages in hepatocellular carcinoma (HCC). A technology of array-based CGH using DNA chips spotted with 1440 BAC clones was applied to 42 surgically removed HCCs to examine the DNA copy number aberrations. A frequent copy number gain was detected on chromosomal regions 1q, 8q and Xq. In particular, gains of 1q42.12, 1q43 and 8q24.3 were detected in more than 65% of tumours. A frequent copy number loss was detected on chromosomal regions 1p, 4q, 6q, 8p and 17p. Losses of 8p21 and 17p13 were detected in more than 55% of HCCs. However, the DNA copy number gains of clones on 6p and 8q24.12 were more frequent in stage III/IV tumours than in stage I/II tumours (p < 0.001). In particular, the gain of the whole 6p was virtually limited to advanced-staged HCCs. The gain of the whole 6p is suggested to be a genomic marker for the late stages in HCCs. These observations therefore support the concept of genomic staging in HCC.
随着癌症进展,基因组畸变以逐步的方式在癌细胞中积累。然而,是否存在与肿瘤进展相关的基因组变化仍不明确。本研究的目的是阐明肝细胞癌(HCC)中基因组改变与临床分期之间的关系。将一种基于DNA芯片的比较基因组杂交(CGH)技术应用于42例手术切除的HCC,该芯片上点样了1440个BAC克隆,以检测DNA拷贝数畸变。在染色体区域1q、8q和Xq检测到频繁的拷贝数增加。特别是,在超过65%的肿瘤中检测到1q42.12、1q43和8q24.3的增加。在染色体区域1p、4q、6q、8p和17p检测到频繁的拷贝数减少。在超过55%的HCC中检测到8p21和17p13的缺失。然而,6p和8q24.12上克隆的DNA拷贝数增加在III/IV期肿瘤中比在I/II期肿瘤中更频繁(p < 0.001)。特别是,整个6p的增加实际上仅限于晚期HCC。整个6p的增加被认为是HCC晚期的一个基因组标志物。因此,这些观察结果支持了HCC中基因组分期的概念。