Suppr超能文献

膀胱癌中6p21.3区域的杂合性缺失及HLA I类分子表型改变

LOH at 6p21.3 region and HLA class I altered phenotypes in bladder carcinomas.

作者信息

Maleno Isabel, Romero Jose Maria, Cabrera Teresa, Paco Laura, Aptsiauri Natalia, Cozar Jose Manuel, Tallada Miguel, López-Nevot Miguel Angel, Garrido Federico

机构信息

Dept. de Análisis Clínicos, Hospital Universitario Virgen de las Nieves, Avd. Fuerzas Armadas 2, 18014, Granada, Spain.

出版信息

Immunogenetics. 2006 Jul;58(7):503-10. doi: 10.1007/s00251-006-0111-8. Epub 2006 May 17.

Abstract

Alterations in HLA class I antigen expression have been frequently described in different epithelial tumors and are thought to favor tumor immune escape from T lymphocyte recognition. Multiple molecular mechanisms are responsible for these altered HLA class I tumor phenotypes. Some are structural defects that produce unresponsiveness to treatment with interferons. Others include alterations in regulatory mechanisms that can be switched on by treatment of tumor cells with different cytokines. One important mechanism belonging to the first group is loss of heterozygosity (LOH) at chromosome region 6p21.3, which can lead to HLA haplotype loss. In this investigation, the frequency of LOH at 6p21 chromosome region was studied in 69 bladder carcinomas. Short tandem repeat analysis showed that 35% of cases had LOH in this chromosome region. By considering these results together with immunohistological findings previously published by our group, we identified a distribution pattern of HLA class I altered phenotypes in bladder cancer. The most frequently altered phenotype in bladder carcinomas was total loss of HLA class I expression (17 cases, 25%), followed by phenotype II associated with HLA haplotype loss (12 cases, 17.5%), and HLA allelic loss (ten cases, 14.5%). Nine cases (13%) were classified as having a compound phenotype, five cases (7%) as having HLA locus loss, and in 16 cases (23%) no alteration in HLA expression was detected. An important conclusion of this report is that a combination of different molecular and immunohistological techniques is required to precisely define which HLA alleles are lost during tumor progression and to characterize the underlying mechanisms of these losses. These studies should be performed when a cancer patient is to be included in an immunotherapy protocol that aims to stimulate different immune effector mechanisms.

摘要

HLA I类抗原表达的改变在不同上皮肿瘤中屡有报道,被认为有利于肿瘤从T淋巴细胞识别中实现免疫逃逸。多种分子机制导致了这些HLA I类肿瘤表型的改变。一些是结构缺陷,导致对干扰素治疗无反应。其他包括调节机制的改变,可通过用不同细胞因子处理肿瘤细胞来开启。属于第一组的一个重要机制是6号染色体区域6p21.3的杂合性缺失(LOH),这可导致HLA单倍型丢失。在本研究中,对69例膀胱癌患者6p21染色体区域的LOH频率进行了研究。短串联重复序列分析显示,35%的病例在该染色体区域存在LOH。结合这些结果以及我们小组先前发表的免疫组织学研究结果,我们确定了膀胱癌中HLA I类改变表型的分布模式。膀胱癌中最常改变的表型是HLA I类表达完全缺失(17例,25%),其次是与HLA单倍型丢失相关的表型II(12例,17.5%),以及HLA等位基因丢失(10例,14.5%)。9例(13%)被归类为具有复合表型,5例(7%)为HLA基因座丢失,16例(23%)未检测到HLA表达改变。本报告的一个重要结论是,需要结合不同的分子和免疫组织学技术来精确确定肿瘤进展过程中哪些HLA等位基因丢失,并表征这些丢失的潜在机制。当癌症患者要纳入旨在刺激不同免疫效应机制的免疫治疗方案时,应进行这些研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验