Li Ming D, Konu Ozien, Kane Justin K, Becker Kevin G
Department of Pharmacology, University of Tennessee College of Medicine, Memphis 38163, USA.
Mol Neurobiol. 2002 Jun;25(3):265-85. doi: 10.1385/MN:25:3:265.
Since its development, microarray technique has revolutionized almost all fields of biomedical research by enabling high-throughput gene expression profiling. Using cDNA microarrays, thousands of genes from various organisms have been examined with respect to differentiation/development, disease diagnosis, and drug discovery Nevertheless, research on nicotine using cDNA microarrays has been rather limited. Therefore, it is our intention in this article to report the findings of our cDNA microarray study on nicotine. We first present an overview of the microarray technology, particularly focusing on the factors related to microarray design and analysis. Second, we provide a detailed description of several newly identified biological pathways in our laboratory, such as phosphatidylinositol signaling and calcium homeostasis, which are involved in response to chronic nicotine administration. Additionally, we illustrate how comparisons between microarray studies help identify candidate genes that potentially may explain the observed inverse association between smoking and schizophrenia. Lastly, given the early stage of microarray research on nicotine, we elaborate on the need for an efficient analysis of genetic networks to further enhance our understanding of the mechanisms involved in nicotine abuse and addiction.
自其发展以来,微阵列技术通过实现高通量基因表达谱分析,彻底改变了生物医学研究的几乎所有领域。利用cDNA微阵列,已经对来自各种生物体的数千个基因进行了关于分化/发育、疾病诊断和药物发现方面的研究。然而,使用cDNA微阵列对尼古丁的研究相当有限。因此,我们在本文中打算报告我们关于尼古丁的cDNA微阵列研究结果。我们首先概述微阵列技术,特别关注与微阵列设计和分析相关的因素。其次,我们详细描述了我们实验室新发现的几种生物途径,如磷脂酰肌醇信号传导和钙稳态,它们参与对慢性尼古丁给药的反应。此外,我们说明了微阵列研究之间的比较如何有助于识别可能解释观察到的吸烟与精神分裂症之间负相关关系的候选基因。最后,鉴于尼古丁微阵列研究尚处于早期阶段,我们阐述了对遗传网络进行有效分析的必要性,以进一步加深我们对尼古丁滥用和成瘾所涉及机制的理解。