Microarray Analysis Identifies a Unique Molecular Signature of Human ThyroidCancer Stem Cells

Reigh-Yi Lin
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引用次数: 2

Abstract

Anaplastic thyroid cancer (ATC) is the most lethal type of thyroid cancer, with a mean survival of six months from the time of diagnosis. Using patient-derived ATC cell lines, we have recently shown that ATC contains a minority population of cancer stem cells that can grow as self-renewing, non-adherent thyrospheres. Compared to bulk tumor cells raised in monolayers, these thyrospheres have increased clonogenic and tumor-initiating potential, and they robustly initiate tumors that closely resemble human ATC when orthotopically implanted into the thyroids of immunodeficient mice. Here we use the Affymetrix GeneChip analysis to identify gene expression differences between thyrospheres and monolayer cells from the human ATC cell line THJ-11T. Our microarray analysis identified a total of 1,659 differentially expressed gene transcripts, many of which have been implicated in key pathways such as those governing cell proliferation, migration, invasion, vasculogenesis, and chemoresistance. These results indicate that thyroid cancer stem cells have a distinct molecular signature. These data will be helpful for the design of future therapeutic strategies that directly target thyroid cancer stem cells.
微阵列分析鉴定了人类甲状腺癌干细胞的独特分子特征
间变性甲状腺癌(ATC)是最致命的甲状腺癌类型,从诊断时起平均生存时间为6个月。利用患者来源的ATC细胞系,我们最近发现ATC含有少数癌症干细胞,它们可以作为自我更新的非粘附性甲状腺细胞生长。与单层培养的大块肿瘤细胞相比,这些甲状腺细胞具有更高的克隆性和肿瘤启动潜力,并且当将其原位植入免疫缺陷小鼠的甲状腺时,它们强烈地启动与人类ATC相似的肿瘤。在这里,我们使用Affymetrix基因芯片分析鉴定了人ATC细胞系THJ-11T甲状腺球和单层细胞之间的基因表达差异。我们的微阵列分析共鉴定了1,659个差异表达基因转录本,其中许多与关键途径有关,如控制细胞增殖、迁移、侵袭、血管发生和化学耐药。这些结果表明甲状腺癌干细胞具有独特的分子特征。这些数据将有助于设计未来直接针对甲状腺癌干细胞的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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