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首页> 外文期刊>Immunogenetics >HLA class I alterations in breast carcinoma are associated with a high frequency of the loss of heterozygosity at chromosomes 6 and 15
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HLA class I alterations in breast carcinoma are associated with a high frequency of the loss of heterozygosity at chromosomes 6 and 15

机译:HLA乳腺癌中的I类改变与染色体6和15的杂合子丧失的高频率相关

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摘要

HLA class I (HLA-I) molecules play a crucial role in the presentation of tumor antigenic peptides to CD8+ T cells. Tumor HLA-I loss provides a route of immune escape from T cell-mediated killing. We analyzed HLA-I expression in 98 cryopreserved breast cancer tissues using a broad panel of anti-HLA-I antibodies. Genomic HLA-I typing was performed using DNA obtained from autologous normal breast tissue. Analysis of the loss of heterozygosity (LOH) in the HLA-I region of chromosome 6 (LOH-6) and in the β2-microglobulin (B2M) region of chromosome 15 (LOH-15) was done by microsatellite amplification of DNA isolated from microdissected tumor areas. B2M gene sequencing was done using this DNA form HLA-I-negative tumors. Immunohistological analysis revealed various types of HLA-I alterations in 79 tumors (81%), including total HLA-I loss in 53 cases (54%) and partial loss in 16 samples (14%). In 19 cases (19%), HLA-I expression was positive. Using microsatellite analysis, we detected LOH in 36 cases out of 92 evaluated (39%), including 15 samples with only LOH-6, 14 with LOH-15, and seven tumors with LOH-6 and LOH-15 at the same time. Remarkably, we detected LOH-6 in eight tumors with positive HLA-I immunolabeling. We did not find any B2M mutations in HLA-I-negative breast tumors. In conclusion, LOH at chromosomes 6 and 15 has a high incidence in breast cancer and occurs in tumors with different HLA-I immunophenotypes. This common molecular mechanism of HLA-I alterations may reduce the ability of cytotoxic T lymphocytes? to kill tumor cells and negatively influence the clinical success of cancer immunotherapy.
机译:HLA类I(HLA-I)分子在肿瘤抗原肽呈递至CD8 + T细胞中起着至关重要的作用。肿瘤HLA-I损失提供了一种免疫逃逸的途径从T细胞介导的杀伤。我们使用宽的抗HLA-1抗体分析了98乳腺癌组织中的HLA-I表达。使用从自体正常乳腺组织中获得的DNA进行基因组HLA-I键入。通过分离的DNA的微卫星扩增来分析染色体6(LOH-6)的HLA-I区和β2-微球蛋白(B2M)区域的杂合性(LOH-15)中的β2-微球蛋白(B2M)区域中的损失微小肿瘤区域。使用该DNA形成HLA-I阴性肿瘤进行B2M基因测序。免疫组织学分析显示出79例肿瘤(81%)中的各种类型的HLA-1改变,包括53例(54%)中的总HLA-I损失,16个样品中的部分损失(14%)。在19例(19%)中,HLA-I表达是阳性的。使用微卫星分析,我们在92例评估(39%)中检测到LOH,其中包括只有LOH-6,14的15个样品,同时具有LOH-6和LOH-15的七种肿瘤。值得注意的是,我们在八个肿瘤中检测到LOH-6,阳性HLA-I免疫标签。我们没有发现HLA-I阴性乳腺肿瘤中的任何B2M突变。总之,染色体6和15的LOH在乳腺癌中具有高发病率,并且发生在具有不同HLA-I免疫胞间型的肿瘤中。这种常见的HLA-I改变的分子机制可降低细胞毒性T淋巴细胞的能力吗?杀死肿瘤细胞并对癌症免疫疗法的临床成功产生负面影响。

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