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肿瘤原代培养物作为药物反应预测模型的可靠性:结直肠癌患者组织与原代培养物的表达谱比较。

Reliability of tumor primary cultures as a model for drug response prediction: expression profiles comparison of tissues versus primary cultures from colorectal cancer patients.

机构信息

Cancer Science Institute of Singapore, National University of Singapore, 28 Medical Drive #02-07, Singapore 117456, Singapore.

出版信息

J Cancer Res Clin Oncol. 2012 Mar;138(3):463-82. doi: 10.1007/s00432-011-1115-9. Epub 2011 Dec 21.

DOI:10.1007/s00432-011-1115-9
PMID:22186935
Abstract

PURPOSE

Since primary tumor cells from patients have been used as a model for assessment of drug response for individual patients, this study aims to evaluate the reliability of such a model in colorectal cancer (CRC) in predicting the response of tumor tissues through comparison of their expression profiles.

METHODS

Establishment of primary cultures from tissues obtained surgically from CRC patients allowed us to study the gene expression differences between normal and tumor tissues as well as primary cultures derived from the tumor mass. The tissues comparison highlights the molecular characteristics of tumors, while the comparison between primary tumor cells versus normal and tumor tissues allowed us to identify alterations associated with the establishment of culture. Genes-drug association analyses allowed us to fine-tune our expectations while using primary culture as a model for drug assessment.

RESULTS

Comparison between tumor cultures and original tissues through functional analyses showed the deregulations caused by culture establishment. Investigating the impact of such changes in genes-drug associations to identify the potential alterations in drug response, we found that primary cultures may have increased susceptibility toward paclitaxel, but reduced susceptibility toward analogues of fluorouracil compared with original tumors.

CONCLUSIONS

Response of primary tumor cells toward different drugs is not linearly associated to tumor tissues. Our results highlight the importance to account for the discrepancy in responses between the primary tumor cells and original counterparts in order to provide clinicians with important insights to improve selection of drugs for individual patients based on in vitro assays.

摘要

目的

由于已经将患者的原代肿瘤细胞用作评估个体患者药物反应的模型,因此本研究旨在通过比较其表达谱,评估该模型在结直肠癌(CRC)中预测肿瘤组织反应的可靠性。

方法

从 CRC 患者手术获得的组织中建立原代培养物,使我们能够研究正常组织与肿瘤组织以及源自肿瘤组织的原代培养物之间的基因表达差异。组织比较突出了肿瘤的分子特征,而原代肿瘤细胞与正常组织和肿瘤组织之间的比较使我们能够确定与培养建立相关的改变。基因-药物关联分析使我们能够在将原代培养物用作药物评估模型时,微调我们的预期。

结果

通过功能分析比较肿瘤培养物和原始组织,显示出培养建立引起的失调。研究这种基因-药物关联变化对药物反应潜在改变的影响,我们发现与原始肿瘤相比,原代培养物对紫杉醇的敏感性可能增加,但对氟尿嘧啶类似物的敏感性降低。

结论

原代肿瘤细胞对不同药物的反应与肿瘤组织没有线性关联。我们的结果强调了在体外测定中,为了为临床医生提供有关根据体外测定为个体患者选择药物的重要见解,必须考虑原代肿瘤细胞与原始对应物之间反应的差异。

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