Lichun Yang, Ching Tang Cecilia Man, Wai Lau Kwok, Lung Maria Li
Department of Biology, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong (SAR), Kowloon, People's Republic of China.
Cancer Lett. 2004 Jan 8;203(1):71-7. doi: 10.1016/j.canlet.2003.09.027.
Multiple and extensive alterations in chromosome 9 were detected in thirty-four esophageal squamous cell carcinoma patients, using seventeen polymorphic markers localized to chromosome 9 to detect the loss of heterozygosity (LOH) by polymerase chain reaction techniques. The LOH rates detected in this study range from 42.9 to 80.0%. Three commonly deleted regions mapping to 9p23-p22, 9q13-q22.3, and 9q34 were observed. D9S1812 LOH at 9q22.1 was significantly associated with well- and moderately-differentiated tumors; LOH at D9S768, mapping to 9q13-21.3, indicated that drinking habits are not a significant risk factor for Chinese esophagus cancer. Interestingly, no case of microsatellite instability was observed.
利用定位于9号染色体上的17个多态性标记,通过聚合酶链反应技术检测杂合性缺失(LOH),在34例食管鳞状细胞癌患者中检测到9号染色体存在多处广泛改变。本研究中检测到的LOH率在42.9%至80.0%之间。观察到三个常见的缺失区域,分别定位于9p23 - p22、9q13 - q22.3和9q34。9q22.1处的D9S1812 LOH与高分化和中分化肿瘤显著相关;定位于9q13 - 21.3的D9S768处的LOH表明,饮酒习惯并非中国食管癌的重要危险因素。有趣的是,未观察到微卫星不稳定性病例。