Kuwahara Yoshitaka, Tanabe Chikako, Ikeuchi Tatsuro, Aoyagi Kazuhiko, Nishigaki Michiko, Sakamoto Hiromi, Hoshinaga Kiyotaka, Yoshida Teruhiko, Sasaki Hiroki, Terada Masaaki
Genetics Division, National Cancer Center Research Institute, Tokyo, Japan.
Genes Chromosomes Cancer. 2004 Oct;41(2):125-32. doi: 10.1002/gcc.20075.
Gene amplification is a common phenomenon in cancer. Cytogenetic analyses have indicated that breakage-fusion-bridge (BFB) cycles drive intrachromosomal amplification of some oncogenes in a head-to-head manner in human cancers. However, the complex structures of an amplified sequence found in cancers are not always explained by the BFB model. At the 17q21 locus, which is not linked to common fragile sites, we discovered a recombination hot spot harboring amplicon repeats in tandem in a head-to-tail orientation, with the interamplicon junctions in each cancer cell being homogeneous. These findings clearly show the presence of alternative mechanisms other than BFB cycles in oncogene amplification.
基因扩增是癌症中的常见现象。细胞遗传学分析表明,断裂-融合-桥(BFB)循环以头对头的方式驱动人类癌症中某些癌基因的染色体内扩增。然而,癌症中发现的扩增序列的复杂结构并不总是能用BFB模型来解释。在与常见脆性位点无关的17q21位点,我们发现了一个重组热点,其中包含以头对尾方向串联的扩增子重复序列,每个癌细胞中的扩增子间连接是均匀的。这些发现清楚地表明,在癌基因扩增中存在除BFB循环之外的其他机制。