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高分辨率比较基因组杂交显示的弥漫型胃癌基因组改变

Genomic alterations in diffuse-type gastric cancer as shown by high-resolution comparative genomic hybridization.

作者信息

Takeno Sylvia Satomi, Leal Mariana Ferreira, Lisboa Luara Carolina Frias, Lipay Mônica Vannucci, Khayat André Salim Nunes, Assumpção Paulo Pimentel, Burbano Rommel Rodríguez, Smith Marília de Arruda Cardoso

机构信息

Genetics Division, Department of Morphology and Genetics, Federal University of São Paulo, Campus São Paulo, Rua Botucatu 740, São Paulo, SP, Brazil.

出版信息

Cancer Genet Cytogenet. 2009 Apr 1;190(1):1-7. doi: 10.1016/j.cancergencyto.2008.09.007.

Abstract

Gastric adenocarcinoma is a serious public health concern, especially in northern Brazil. Gastric cancer can be subdivided into diffuse and intestinal types. Genetic imbalances in diffuse-type gastric cancer remain largely unknown. In the present study, we analyzed 24 advanced diffuse-type gastric cancer samples from northern Brazil subjects using high-resolution comparative genomic hybridization. We found chromosomal alterations in 75% of samples. In cancers with aneusomies, the mean genomic copy number alteration was 6.4. Losses of chromosome regions exceeded gains. The most frequent losses were located at chromosome regions 11q and 18q (five samples for each region), 1pq, 3q, 4q, 5q, 13q, and 14q (four samples), followed by 2pq, 7p, 9pq, 11p, and 16p (three samples). Our results confirm that gastric cancer has a complex pattern of chromosomal alterations that can be due to general chromosomal instability related to the advanced stage of gastric carcinogenesis. Loss of 11q and 18q were the most frequent chromosomal changes in diffuse-type gastric adenocarcinoma in individuals from northern Brazil. Frequent loss of 11q chromosome region in this gastric cancer may be peculiar among this population.

摘要

胃腺癌是一个严重的公共卫生问题,在巴西北部地区尤为如此。胃癌可分为弥漫型和肠型。弥漫型胃癌中的基因失衡情况在很大程度上仍不为人知。在本研究中,我们使用高分辨率比较基因组杂交技术分析了24例来自巴西北部地区受试者的晚期弥漫型胃癌样本。我们发现75%的样本存在染色体改变。在出现非整倍体的癌症中,平均基因组拷贝数改变为6.4。染色体区域的缺失超过了增加。最常见的缺失位于染色体区域11q和18q(每个区域有5个样本)、1pq、3q、4q、5q、13q和14q(4个样本),其次是2pq、7p、9pq、11p和16p(3个样本)。我们的结果证实,胃癌具有复杂的染色体改变模式,这可能是由于与胃癌发生晚期相关的一般染色体不稳定性所致。11q和18q的缺失是巴西北部地区个体弥漫型胃腺癌中最常见的染色体变化。该胃癌中11q染色体区域的频繁缺失在这一人群中可能较为特殊。

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