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透明肾细胞癌中与6号染色体区域6p21杂合性缺失相关的HLA单倍型缺失频率较低。

Low frequency of HLA haplotype loss associated with loss of heterozygocity in chromosome region 6p21 in clear renal cell carcinomas.

作者信息

Maleno Isabel, Lopez Nevot Miguel Angel, Seliger Barbara, Garrido Federico

机构信息

Departmento Analisis Clinicos, Hospital Universitario Virgen Nieves, Granada, Spain.

出版信息

Int J Cancer. 2004 Apr 20;109(4):636-8. doi: 10.1002/ijc.20000.

Abstract

HLA class I loss or downregulation is a widespread mechanism used by tumor cells to avoid tumor recognition by cytotoxic T lymphocytes favoring tumor immune escape. Multiple molecular mechanisms are responsible for these altered HLA class I tumor phenotypes. It has been described in different epithelial tumors that loss of heterozygosity (LOH) at chromosome region 6p21.3 is a frequent mechanism that leads to HLA haplotype loss, ranging between 40 and 50%, depending on the tumor entity analyzed. Here we have tested the frequency of LOH at 6p21 chromosome region in Renal Cell Carcinomas (RCC) of the clear cell and chromophobe subtype. A low frequency of HLA haplotype loss (6.6%) was found in clear cell RCC. These data significantly differ from those reported in other epithelial tumors. In contrast, in RCC of chromophobe subtype this frequency was 10 times higher (3 out of 5 cases analyzed). These results indicate that LOH at 6p21.3 is not a frequent mechanism that leads to HLA class I abnormalities in clear cell RCC. In addition, the chromophobe RCC subtypes differ not only in histopathological criteria but also in the frequency of LOH-mediating HLA class I alterations. These results might help to understand the significantly different biological behavior of both RCC subtypes.

摘要

HLA I类分子缺失或下调是肿瘤细胞用于逃避细胞毒性T淋巴细胞对肿瘤的识别从而促进肿瘤免疫逃逸的一种广泛机制。多种分子机制导致了这些改变的HLA I类肿瘤表型。在不同的上皮性肿瘤中已发现,6号染色体区域6p21.3的杂合性缺失(LOH)是导致HLA单倍型缺失的常见机制,根据所分析的肿瘤实体不同,其发生率在40%至50%之间。在此,我们检测了透明细胞和嫌色细胞亚型肾细胞癌(RCC)中6p21染色体区域的LOH频率。在透明细胞RCC中发现HLA单倍型缺失的频率较低(6.6%)。这些数据与其他上皮性肿瘤报道的数据显著不同。相比之下,在嫌色细胞亚型RCC中,该频率高出10倍(分析的5例中有3例)。这些结果表明,6p21.3处的LOH并非导致透明细胞RCC中HLA I类异常的常见机制。此外,嫌色细胞RCC亚型不仅在组织病理学标准上不同,而且在由LOH介导的HLA I类改变的频率上也不同。这些结果可能有助于理解这两种RCC亚型显著不同的生物学行为。

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