Jacquemier Jocelyne, Ginestier Christophe, Bertucci François, Jauffret Emmanuelle Charafe, Geneix Jeanine, Birnbaum Daniel
Département d'oncologie moléculaire, Institut Paoli-Calmettes, 232, bd de Sainte-Marguerite, 13273 Marseille Cedex 9.
Bull Cancer. 2003 Jan;90(1):31-8.
The progress in the knowledge of molecular genetics and the availability of high-throughput technologies offer the opportunity to identify new diagnostic and prognostic markers and new therapeutic targets in human cancer. The recently developed "tissue microarraysî (TMA) technology allows parallel molecular profiling of clinical samples. Using this technique and immunohistochemistry (IHC), fluorescence in situ hybridisation (FISH), or RNA in situ hybridisation (ISH), the pathologist is now able to perform unprecedented large-scale analyses. The advantages are significant: large number of cases assessed simultaneously for numerous markers, processing in identical conditions, reduced amount of archival tissues, excellent correlation with standard methods, reduction in cost and time. This article provides a short review of this technology, and points out several aspects of the TMA construction and its applications for clinical research.
分子遗传学知识的进步以及高通量技术的应用,为识别人类癌症新的诊断和预后标志物以及新的治疗靶点提供了契机。最近开发的“组织微阵列”(TMA)技术能够对临床样本进行平行分子分析。利用该技术及免疫组织化学(IHC)、荧光原位杂交(FISH)或RNA原位杂交(ISH),病理学家现在能够进行前所未有的大规模分析。其优势显著:可同时对大量病例的众多标志物进行评估,在相同条件下处理,减少存档组织用量,与标准方法相关性良好,降低成本和时间。本文对该技术进行简要综述,并指出TMA构建及其在临床研究中的应用的几个方面。