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对源自rasV12/E1A转化的小鼠胚胎成纤维细胞的肿瘤进行基因表达谱分析,以鉴定肿瘤发生所需的基因。

Gene expression profiling of tumours derived from rasV12/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development.

作者信息

Vasseur Sophie, Malicet Cédric, Calvo Ezequiel L, Dagorn Jean Charles, Iovanna Juan L

机构信息

INSERM U,624, Stress Cellulaire, 163 Avenue de Luminy, Case 915, Parc Scientifique et Technologique de Luminy, 13288 Marseille Cedex 9, France.

出版信息

Mol Cancer. 2005 Jan 16;4(1):4. doi: 10.1186/1476-4598-4-4.

Abstract

BACKGROUND

In cancer, cellular transformation is followed by tumour development. Knowledge on the mechanisms of transformation, involving activation of proto-oncogenes and inactivation of tumour-suppressor genes has considerably improved whereas tumour development remains poorly understood. An interesting way of gaining information on tumour progression mechanisms would be to identify genes whose expression is altered during tumour formation. We used the Affymetrix-based DNA microarray technology to analyze gene expression profiles of tumours derived from rasV12/E1A-transformed mouse embryo fibroblasts in order to identify the genes that could be involved in tumour development.

RESULTS

Among the 12,000 genes analyzed in this study, only 489 showed altered expression during tumour development, 213 being up-regulated and 276 down-regulated. The genes differentially expressed are involved in a variety of cellular functions, including control of transcription, regulation of mRNA maturation and processing, regulation of protein translation, activation of interferon-induced genes, intracellular signalling, apoptosis, cell growth, angiogenesis, cytoskeleton, cell-to-cell interaction, extracellular matrix formation, metabolism and production of secretory factors.

CONCLUSIONS

Some of the genes identified in this work, whose expression is altered upon rasV12/E1A transformation of MEFs, could be new cancer therapeutic targets.

摘要

背景

在癌症中,细胞转化之后是肿瘤发展。关于涉及原癌基因激活和肿瘤抑制基因失活的转化机制的知识有了显著提高,而肿瘤发展仍知之甚少。获取肿瘤进展机制信息的一种有趣方法是识别在肿瘤形成过程中表达发生改变的基因。我们使用基于Affymetrix的DNA微阵列技术分析源自rasV12/E1A转化的小鼠胚胎成纤维细胞的肿瘤的基因表达谱,以识别可能参与肿瘤发展的基因。

结果

在本研究分析的12000个基因中,只有489个在肿瘤发展过程中表达发生改变,其中213个上调,276个下调。差异表达的基因涉及多种细胞功能,包括转录控制、mRNA成熟和加工的调节、蛋白质翻译的调节、干扰素诱导基因的激活、细胞内信号传导、细胞凋亡、细胞生长、血管生成、细胞骨架、细胞间相互作用、细胞外基质形成、代谢和分泌因子的产生。

结论

在这项工作中鉴定出的一些基因,其在MEF的rasV12/E1A转化后表达发生改变,可能是新的癌症治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3490/546195/43b3dba493ec/1476-4598-4-4-1.jpg

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