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不平衡易位,一种导致人类肺癌杂合性缺失的主要染色体改变。

Unbalanced translocation, a major chromosome alteration causing loss of heterozygosity in human lung cancer.

作者信息

Ogiwara H, Kohno T, Nakanishi H, Nagayama K, Sato M, Yokota J

机构信息

Biology Division, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.

出版信息

Oncogene. 2008 Aug 14;27(35):4788-97. doi: 10.1038/onc.2008.113. Epub 2008 Apr 14.

Abstract

Loss of heterozygosity (LOH) is a major genetic event causing inactivation of tumor suppressor genes in human carcinogenesis. To elucidate chromosomal mechanisms causing LOH, 201 LOHs in 10 cases of human lung cancer, which were detected by a genome-wide single nucleotide polymorphism array analysis, were investigated for responsible chromosome alterations by integrating information on breakpoints for DNA copy number changes obtained by array-comparative genome hybridization and on numerical and structural chromosomal alterations obtained by spectral karyotyping. The majority (80%) of LOHs were partial chromosome LOHs caused by structural chromosomal alterations, while the remaining (20%) were whole chromosome LOHs caused by whole chromosome deletions. Unbalanced translocation was defined as the most frequent alteration, and it accounted for 30% of all LOHs. Three other structural alterations-interstitial deletion (19%), mitotic recombination (9%) and gene conversion (6%)-also contributed to the occurrence of LOH, while terminal deletion contributed to only a small subset (1%). Since unbalanced translocation is a common chromosomal alteration in lung cancer cells, the results in the present study strongly indicate that a considerable fraction of LOHs detected in lung cancer cells are caused by unbalanced translocation.

摘要

杂合性缺失(LOH)是人类致癌过程中导致肿瘤抑制基因失活的主要遗传事件。为了阐明导致LOH的染色体机制,我们通过整合阵列比较基因组杂交获得的DNA拷贝数变化断点信息以及光谱核型分析获得的染色体数目和结构改变信息,对通过全基因组单核苷酸多态性阵列分析检测到的10例人类肺癌中的201个LOH进行了研究,以寻找相关的染色体改变。大多数(80%)的LOH是由染色体结构改变引起的部分染色体LOH,而其余(20%)是由整条染色体缺失引起的整条染色体LOH。不平衡易位被确定为最常见的改变,占所有LOH的30%。其他三种结构改变——间质缺失(19%)、有丝分裂重组(9%)和基因转换(6%)——也促成了LOH的发生,而末端缺失仅导致一小部分(1%)。由于不平衡易位是肺癌细胞中常见的染色体改变,本研究结果强烈表明,在肺癌细胞中检测到的相当一部分LOH是由不平衡易位引起的。

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