Jacquemier Jocelyne, Ginestier Christophe, Charafe-Jauffret Emmanuelle, Bertucci François, Bege Thierry, Geneix Jeanine, Birnbaum Daniel
Département d'Oncologie Moléculaire, Institut Paoli-Calmettes, 232 Bd de Sainte Marguerite, 13273 Marseille Cedex 9, France.
Ann Pathol. 2003 Dec;23(6):623-32.
Progress in the knowledge of molecular genetics and 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 microarrays" (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, processed in identical conditions, from reduced amount of archival tIssues, with an excellent correlation with standard methods, and a 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展以及高通量技术的可用性为识别人类癌症中的新诊断和预后标志物及新治疗靶点提供了机会。最近开发的“组织微阵列”(TMA)技术允许对临床样本进行平行分子分析。利用该技术和免疫组织化学(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,所需存档组织量减少,与标准方法具有良好的相关性,且成本和时间降低。本文对该技术进行了简要综述,并指出了TMA构建及其在临床研究中的应用的几个方面。