Departamento de Bioquímica, Instituto de Química –USP, São Paulo, Brasil.
Curr Pharm Biotechnol. 2011 Nov;12(11):1881-90. doi: 10.2174/138920111798377102.
During the past few years, Epithelial-Mesenchymal Transition (EMT) has emerged as one of the most hot spots in clinical research. Its existence in human tumors can form the basis for explaining characteristics of cancer progression and metastasis, as well as certain cases of drug resistance and relapses after treatment. These cellular responses are tightly regulated by intracellular signaling pathways evoked by humoral factors that include growth factors, chemokines and cytokines. Indeed, several gene regulatory programs known to promote EMT during development have recently been discovered to play key roles in cancer progression. A deeper understanding of the cellular and molecular basis of these different programs should aid in both the development of better diagnosis methods, as well as of specific treatments for invasive cancer. In this review we set out to summarize recent novel insights into the molecular players underlying EMT and its relation with cancer progression and metastasis.
在过去的几年中,上皮-间充质转化(EMT)已成为临床研究的热点之一。其在人类肿瘤中的存在可以为解释癌症进展和转移的特征以及某些情况下治疗后耐药和复发的原因提供依据。这些细胞反应受到体液因子(包括生长因子、趋化因子和细胞因子)激活的细胞内信号通路的严格调控。事实上,最近发现了几种已知在发育过程中促进 EMT 的基因调控程序,它们在癌症进展中发挥着关键作用。深入了解这些不同程序的细胞和分子基础,将有助于开发更好的诊断方法以及针对侵袭性癌症的特定治疗方法。在这篇综述中,我们总结了 EMT 的分子基础及其与癌症进展和转移的关系的最新研究进展。