日本人原代培养肾皮质细胞基因表达的个体差异

A. Sasaki, Y. Oshima, Saeko Kishimoto, Akio Fujimura
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引用次数: 0

摘要

我们使用微阵列来检测源自日本受试者的肾小管细胞原代培养中基因表达的个体差异。患者均为肾或尿路单发肿瘤,病理诊断为肾细胞癌或移行细胞癌。从组织的非肿瘤部分采集的肾组织样本被认为是正常组织,因为从临床实验室数据来看,没有异常的显微镜发现和肾功能障碍的证据。采用Affymetrix基因芯片HG-U133A和HG-U133B阵列分析了9个人肾细胞培养物的全基因组基因表达谱。约有8500个转录本在被试中表现出显著差异表达(p < 0.05),其中1338个转录本变异系数大于50%。其中一些转录物编码药物代谢酶(如UGT1A8和UGT1A9)或钠/磷酸盐共转运蛋白(如PDZK1)。这些数据为利用原代培养的日本受试者肾皮质细胞进行毒性基因组学研究提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Individual Differences in Gene Expression in Primary Cultured Renal Cortex Cells Derived from Japanese Subjects
We used microarrays to examine individual-based differences in gene expression in primary cultures of renal tubular cells derived from Japanese subjects. The subjects had solitary tumors in the kidney or urinary tract, which were diagnosed pathologically as renal cell carcinoma or transitional cell carcinoma. Renal tissue samples collected from a non-tumorous portion of the tissue were regarded as normal tissues, as there were no abnormal microscopic findings and no evidence of renal dysfunction from the clinical laboratory data. The genome-wide gene expression profiles of nine human renal cell cultures were analyzed using the Affymetrix GeneChip HG-U133A and HG-U133B arrays. Approximately 8, 500 transcripts exhibited significant differential expression (p < 0.05) among the subjects, and the coefficients of variation for 1, 338 transcripts were greater than 50%. Some of these transcripts encode drug-metabolizing enzymes (e.g., UGT1A8 and UGT1A9) or sodium/phosphate cotransporters (e.g., PDZK1). These data provide the basis for toxicogenomic studies using primary cultured renal cortical cells from Japanese subjects.
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