Jolly Mohit Kumar, Ware Kathryn E, Gilja Shivee, Somarelli Jason A, Levine Herbert
Center for Theoretical Biological Physics, Rice University, Houston, TX, USA.
Duke Cancer Institute & Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Mol Oncol. 2017 Jul;11(7):755-769. doi: 10.1002/1878-0261.12083. Epub 2017 Jun 12.
Epithelial-to-mesenchymal transition (EMT) and its reverse mesenchymal-to-epithelial transition (MET) have been suggested to play crucial roles in metastatic dissemination of carcinomas. These phenotypic transitions between states are not binary. Instead, carcinoma cells often exhibit a spectrum of epithelial/mesenchymal phenotype(s). While epithelial/mesenchymal plasticity has been observed preclinically and clinically, whether any of these phenotypic transitions are indispensable for metastatic outgrowth remains an unanswered question. Here, we focus on epithelial/mesenchymal plasticity in metastatic dissemination and propose alternative mechanisms for successful dissemination and metastases beyond the traditional EMT/MET view. We highlight multiple hypotheses that can help reconcile conflicting observations, and outline the next set of key questions that can offer valuable insights into mechanisms of metastasis in multiple tumor models.
上皮-间质转化(EMT)及其反向的间质-上皮转化(MET)被认为在癌转移扩散中起关键作用。这些状态之间的表型转变并非二元性的。相反,癌细胞通常表现出一系列上皮/间质表型。虽然上皮/间质可塑性已在临床前和临床中观察到,但这些表型转变中的任何一种对于转移灶的生长是否不可或缺仍是一个未解决的问题。在这里,我们关注转移扩散中的上皮/间质可塑性,并提出超越传统EMT/MET观点的成功扩散和转移的替代机制。我们强调了多个有助于调和相互矛盾观察结果的假设,并概述了下一组关键问题,这些问题可为多种肿瘤模型中的转移机制提供有价值的见解。