Zaravinos Apostolos
Department of Laboratory Medicine, Karolinska Institutet Huddinge, 171 77 Stockholm, Sweden.
J Oncol. 2015;2015:865816. doi: 10.1155/2015/865816. Epub 2015 Mar 25.
The epithelial to mesenchymal transition (EMT) is a powerful process in tumor invasion, metastasis, and tumorigenesis and describes the molecular reprogramming and phenotypic changes that are characterized by a transition from polarized immotile epithelial cells to motile mesenchymal cells. It is now well known that miRNAs are important regulators of malignant transformation and metastasis. The aberrant expression of the miR-200 family in cancer and its involvement in the initiation and progression of malignant transformation has been well demonstrated. The metastasis suppressive role of the miR-200 members is strongly associated with a pathologic EMT. This review describes the most recent advances regarding the influence of miRNAs in EMT and the control they exert in major signaling pathways in various cancers. The ability of the autocrine TGF-β/ZEB/miR-200 signaling regulatory network to control cell plasticity between the epithelial and mesenchymal state is further discussed. Various miRNAs are reported to directly target EMT transcription factors and components of the cell architecture, as well as miRNAs that are able to reverse the EMT process by targeting the Notch and Wnt signaling pathways. The link between cancer stem cells and EMT is also reported and the most recent developments regarding clinical trials that are currently using anti-miRNA constructs are further discussed.
上皮-间质转化(EMT)是肿瘤侵袭、转移和肿瘤发生过程中的一个重要过程,它描述了分子重编程和表型变化,其特征是从极化的静止上皮细胞转变为可移动的间质细胞。现在众所周知,微小RNA(miRNA)是恶性转化和转移的重要调节因子。miR-200家族在癌症中的异常表达及其在恶性转化起始和进展中的作用已得到充分证实。miR-200成员的转移抑制作用与病理性EMT密切相关。本综述描述了miRNA在EMT中的影响及其对各种癌症主要信号通路的调控方面的最新进展。进一步讨论了自分泌转化生长因子-β(TGF-β)/锌指E盒结合蛋白(ZEB)/miR-200信号调节网络控制上皮和间质状态之间细胞可塑性的能力。据报道,各种miRNA可直接靶向EMT转录因子和细胞结构成分,以及通过靶向Notch和Wnt信号通路来逆转EMT过程的miRNA。还报道了癌症干细胞与EMT之间的联系,并进一步讨论了目前使用抗miRNA构建体的临床试验的最新进展。