Liu Teng-fei, Yin Zhi-hua, Gan Run-liang, Zhao Qiang, Dong Lin, Zhou Jian-guo, Dong Bi-hua
Cancer Institute, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Jul;28(7):1229-32.
To obtain allelic loss mapping and define the minimal lost region on chromosome 1q21 in gastric carcinomas, and explore role of 1q21 loss of heterozygosity (LOH) in the development and progression of gastric carcinogenesis.
Using 7 high-density microsatellite markers and PCR method, lq21 LOH was analyzed in 30 paired specimens of fresh gastric carcinoma, and the relation between 1q21 LOH and the clinicopathological features of the malignancy was tested.
The LOH frequency on chromosome 1q21 from these gastric carcinoma tissues reached 60% (18/30). The LOH frequencies of the microsatellite markers D1S514, D1S2696, D1S498, D1S305, D1S2624, D1S2635 and D1S2702 were 13.3%, 10%, 20%, 23.3%, 33.3%, 40% and 23.3%, respectively. The minimal lost region on 1q21 LOH in the gastric carcinoma tissues was located in the region between D1S2624 and D1S2707, in the vicinity of D1S2635. No significant relations of 1q21 LOH to the patients' age, gender, location of the primary foci, clinical staging, or the tumor differentiation were noted (P>0.05), but 1q21 LOH was correlated to lymph node metastases of the malignancy (P<0.05).
Higher frequency of 1q21 LOH occurs in gastric carcinoma cells, suggesting the presence of potential tumor suppressor genes closely associated with gastric carcinogenesis near the region of D1S2635.
获得等位基因缺失图谱并确定胃癌中1q21染色体上的最小缺失区域,探讨1q21杂合性缺失(LOH)在胃癌发生发展过程中的作用。
采用7个高密度微卫星标记和PCR方法,对30对新鲜胃癌标本进行1q21 LOH分析,并检测1q21 LOH与恶性肿瘤临床病理特征之间的关系。
这些胃癌组织中1q21染色体上的LOH频率达到60%(18/30)。微卫星标记D1S514、D1S2696、D1S498、D1S305、D1S2624、D1S2635和D1S2702的LOH频率分别为13.3%、10%、20%、23.3%、33.3%、40%和23.3%。胃癌组织中1q21 LOH的最小缺失区域位于D1S2624和D1S2707之间,靠近D1S2635。未发现1q21 LOH与患者年龄、性别、原发灶位置、临床分期或肿瘤分化之间存在显著关系(P>0.05),但1q21 LOH与恶性肿瘤的淋巴结转移相关(P<0.05)。
胃癌细胞中1q21 LOH频率较高,提示在D1S2635区域附近存在与胃癌发生密切相关的潜在抑癌基因。