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转移性骨肉瘤的基因表达在体外和体内存在差异。

Metastatic osteosarcoma gene expression differs in vitro and in vivo.

作者信息

Lisle Jennifer W, Choi Joseph Y, Horton Jason A, Allen Matthew J, Damron Timothy A

机构信息

Department of Orthopedic Surgery, Musculoskeletal Sciences Research Center, SUNY Upstate Medical University, Suite 130, 550 Harrison Street, Syracuse, NY 13202, USA.

出版信息

Clin Orthop Relat Res. 2008 Sep;466(9):2071-80. doi: 10.1007/s11999-008-0309-1. Epub 2008 May 31.

DOI:10.1007/s11999-008-0309-1
PMID:18516656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2493017/
Abstract

An understanding of differential gene expression in highly metastatic osteosarcoma could provide gene targets for treatment of metastases. We compared gene expression profiles of high- (LM7) and low- (LM2) metastatic SaOS2-derived cell lines in an in vitro tissue culture model and examined several differentially regulated genes in vivo in a murine orthotopic xenograft model. We hypothesized an orthotopic inoculation of LM2 and LM7 cells would establish a primary lesion and the gene expression profile of cells grafted in this fashion would resemble the gene expression profile observed in an in vitro model. Thirty-five days after inoculation, animals were euthanized and both tibiae were harvested and rapidly frozen in liquid nitrogen. Human-specific GAPDH mRNA was present in two of four tibias inoculated with LM2 cells and three of four tibias inoculated with LM7 cells. Tibiae displaying the presence of human cells were assayed by semiquantitative reverse transcriptase polymerase chain reaction. We observed poor correspondence of in vitro to in vivo gene expression for either cell line. Accordingly, in vitro osteosarcoma gene expression data must be interpreted with caution until confirmed in vivo. Our orthotopic injection model allowed in vivo study of differential gene expression between these two cell lines but did not show radiographic evidence of an established primary lesion.

摘要

了解高转移性骨肉瘤中的差异基因表达可为转移瘤的治疗提供基因靶点。我们在体外组织培养模型中比较了高转移性(LM7)和低转移性(LM2)的源自SaOS2的细胞系的基因表达谱,并在小鼠原位异种移植模型中在体内检测了几个差异调节的基因。我们假设原位接种LM2和LM7细胞会形成原发性病变,以这种方式移植的细胞的基因表达谱将类似于在体外模型中观察到的基因表达谱。接种后35天,对动物实施安乐死并采集双侧胫骨,迅速在液氮中冷冻。在接种LM2细胞的四只胫骨中有两只以及接种LM7细胞的四只胫骨中有三只检测到了人特异性甘油醛-3-磷酸脱氢酶(GAPDH)mRNA。对显示有人细胞存在的胫骨进行半定量逆转录聚合酶链反应检测。我们观察到,两种细胞系的体外基因表达与体内基因表达之间的对应性均较差。因此,在体内得到证实之前,体外骨肉瘤基因表达数据的解读必须谨慎。我们的原位注射模型能够在体内研究这两种细胞系之间的差异基因表达,但未显示出已形成原发性病变的影像学证据。

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本文引用的文献

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