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韩国肝细胞癌患者10号染色体长臂23区杂合性缺失及10号染色体缺失的磷酸酶及张力蛋白同源物肿瘤抑制基因突变

Loss of heterozygosity on chromosome 10q23 and mutation of the phosphatase and tensin homolog deleted from chromosome 10 tumor suppressor gene in Korean hepatocellular carcinoma patients.

作者信息

Bae Jei-Jun, Rho Jin-Woo, Lee Tae-Jin, Yun Sung-Su, Kim Hong-Jin, Choi Joon-Hyuk, Jeong Daewon, Jang Byeong-Churl, Lee Tae-Yoon

机构信息

Department of Microbiology, College of Medicine, Yeungnam University, Daegu 705-717, Korea.

出版信息

Oncol Rep. 2007 Oct;18(4):1007-13.

Abstract

Loss of heterozygosity (LOH) in the 10q23 chromosomal region was analyzed in 18 tissue samples from Korean hepatocellular carcinoma (HCC) patients. LOH at the phosphatase and tensin homolog deleted from chromosome 10 (PTEN) region (D10S215, AFMa086wg9 and D10S541) was found in 8 of the 18 (44.4%) HCCs. LOH (20%) and microsatellite instability (26.7%) were also frequently found at the D10S2177 locus, which is located on the telomere side of the PTEN region. LOH was found in other loci, such as AFM280we1 and D10S2281. The presence of LOH in regions other than the PTEN region on chromosome 10q23 suggested the presence of additional tumor suppressor gene(s). PTEN mutation was found in only a subset of HCCs: A single base insertion at the end of the 5'-end splice signal (AG-GUAAGUU) in intron 5 and a silent mutation in exon 6 (codon 188, CTG-Val to CTA). Our data collectively suggest that the genetic alterations of chromosome 10q23, including the PTEN gene, could be important in hepatocarcinogenesis in the Korean population.

摘要

对18例韩国肝细胞癌(HCC)患者的组织样本进行了10q23染色体区域杂合性缺失(LOH)分析。在18例HCC中的8例(44.4%)中发现了10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)区域(D10S215、AFMa086wg9和D10S541)的LOH。在位于PTEN区域端粒侧的D10S2177位点也经常发现LOH(20%)和微卫星不稳定性(26.7%)。在其他位点如AFM280we1和D10S2281也发现了LOH。10q23染色体上PTEN区域以外的区域存在LOH提示存在其他肿瘤抑制基因。仅在一部分HCC中发现了PTEN突变:内含子5中5'-端剪接信号(AG-GUAAGUU)末端的单个碱基插入以及外显子6中的沉默突变(密码子188,CTG-Val变为CTA)。我们的数据共同表明,包括PTEN基因在内的10q23染色体的基因改变在韩国人群的肝癌发生中可能很重要。

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