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中国食管鳞状细胞癌中6p21杂合性缺失与HLA I类分子表达情况

Loss of heterozygosity at 6p21 and HLA class I expression in esophageal squamous cell carcinomas in China.

作者信息

Zhao Xiaogang, Sun Qifeng, Tian Hui, Cong Bo, Jiang Xingtao, Peng Chuanliang

机构信息

Thoracic Surgery, Second Hospital of Shandong University, Jinan, China.

出版信息

Asian Pac J Cancer Prev. 2011;12(10):2741-5.

Abstract

BACKGROUND AND OBJECTIVE

The loss or downregulation of human leukocyte antigen ( HLA-I) has been proposed to contribute to immune evasion by cancer cells. Since the human leukocyte antigen (HLA-I) complex is located at 6p21.3, loss of heterozygosity of this region may alter HLA class I tumor phenotypes. The aim of this study was to analysis loss of heterozygosity (LOH) of chromosome 6p in ESCC samples and correlate this with HLA class I expression.

MATERIALS AND METHODS

A total of 87 formalin-fixed, paraffin-embeded and frozen-fresh of ECSS lesions were collected. HLA-Iand antigen-processing machinery component expression was investigated by immunohistochemistry with anti-HLA class I monoclonal antibody and a panel of 49 ESCCs with downregulated HLA class I expression were selected for LOH studies using 3 microsatellite markers located at 6p21.3 (D6S105,D6S265,D6S273).

RESULTS

HLA-Iantigen,TAP1 and LMP were lost or down-regulated in 57.5, 29.8 and 47.0% of the ESCC lesions, respectively. In 23/49(46.9%) of the ESCCs, allelic loss for at least one locus at 6p21.3 was found.

CONCLUSIONS

Our data show that downregulation of HLA class I expression is correlated with loss of heterozygosity regions at 6p21.3 in ESCC.

摘要

背景与目的

已有研究提出人类白细胞抗原(HLA-I)的缺失或下调有助于癌细胞逃避免疫。由于人类白细胞抗原(HLA-I)复合体位于6p21.3,该区域杂合性缺失可能会改变HLA I类肿瘤表型。本研究的目的是分析食管鳞状细胞癌(ESCC)样本中6号染色体p臂的杂合性缺失(LOH)情况,并将其与HLA I类表达相关联。

材料与方法

共收集了87例经福尔马林固定、石蜡包埋以及冷冻新鲜的ESCC病变样本。采用抗HLA I类单克隆抗体通过免疫组织化学法研究HLA-I及抗原加工机制成分的表达,并使用位于6p21.3的3个微卫星标记(D6S105、D6S265、D6S273),选择49例HLA I类表达下调的ESCC进行LOH研究。

结果

在ESCC病变中,HLA-I抗原、TAP1和LMP的缺失或下调分别占57.5%、29.8%和47.0%。在49例ESCC中的23例(46.9%)中,发现6p21.3至少一个位点存在等位基因缺失。

结论

我们的数据表明,ESCC中HLA I类表达下调与6p21.3杂合性缺失区域相关。

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