Lu Y J, Dong X Y, Shipley J, Zhang R G, Cheng S J
Department of Cancer Etiology, Cancer Institute (Hospital), CAMS and PUMC, Beijing, PR China.
Lung Cancer. 1999 Jan;23(1):61-6. doi: 10.1016/s0169-5002(98)00093-2.
The chromosomal imbalances in nine cases of primary non-small cell lung cancer (NSCLC) and two cell lines derived from normal human bronchial epithelial (HBE) tissue were identified by comparative genomic hybridization (CGH). Gain of material from 3q and loss of 3p material were the most frequent changes in the primary tumors. Other commonly found imbalances included gain of material from 1q, 7p, 8q, 9q, 17q and 20q, and losses involving 4, 5q, 8p, 10 and 13q. High level gain was found in two cases, both encompassing the 3q23-q27 region. Loss of 3p was also found in both of the HBE cell lines suggesting that loss of one or more tumor supressor genes on 3p may be important for epithelial transformation and could be involved in the earlier stages of lung cancer development.
通过比较基因组杂交(CGH)鉴定了9例原发性非小细胞肺癌(NSCLC)以及源自正常人支气管上皮(HBE)组织的两个细胞系中的染色体失衡情况。3q物质增加和3p物质缺失是原发性肿瘤中最常见的变化。其他常见的失衡包括1q、7p、8q、9q、17q和20q物质增加,以及涉及4、5q、8p、10和13q的缺失。在两例中发现了高水平的增加,均包含3q23 - q27区域。在两个HBE细胞系中也发现了3p缺失,这表明3p上一个或多个肿瘤抑制基因的缺失可能对上皮细胞转化很重要,并且可能参与肺癌发展的早期阶段。