School of Life Sciences and Health, University of Roehampton, London SW15 4JD, UK.
Cells. 2022 Feb 13;11(4):649. doi: 10.3390/cells11040649.
In solid tumours, cancer cells that undergo epithelial mesenchymal transition (EMT) express characteristic gene expression signatures that promote invasive migration as well as the development of stemness, immunosuppression and drug/radiotherapy resistance, contributing to the formation of currently untreatable metastatic tumours. The cancer traits associated with EMT can be controlled by the signalling nodes at characteristic adhesion sites (focal contacts, invadopodia and microtentacles) where the regulation of cell migration, cell cycle progression and pro-survival signalling converge. In haematological tumours, ample evidence accumulated during the last decade indicates that the development of an EMT-like phenotype is indicative of poor disease prognosis. However, this EMT phenotype has not been directly linked to the assembly of specific forms of adhesions. In the current review we discuss the role of EMT in haematological malignancies and examine its possible link with the progression towards more invasive and aggressive forms of these tumours. We also review the known types of adhesions formed by haematological malignancies and speculate on their possible connection with the EMT phenotype. We postulate that understanding the architecture and regulation of EMT-related adhesions will lead to the discovery of new therapeutic interventions to overcome disease progression and resistance to therapies.
在实体肿瘤中,经历上皮间质转化(EMT)的癌细胞表达特征性基因表达谱,促进侵袭性迁移以及干性、免疫抑制和药物/放射治疗耐药性的发展,导致目前无法治疗的转移性肿瘤的形成。与 EMT 相关的癌症特征可以通过特征性粘附位点(粘着斑、侵袭伪足和微绒毛)的信号节点来控制,其中细胞迁移、细胞周期进程和促生存信号的调节汇聚在一起。在血液系统肿瘤中,过去十年积累的大量证据表明,EMT 样表型的发展预示着疾病预后不良。然而,这种 EMT 表型尚未与特定形式的粘附物的组装直接相关。在当前的综述中,我们讨论了 EMT 在血液系统恶性肿瘤中的作用,并探讨了其与这些肿瘤向更具侵袭性和侵袭性形式进展的可能联系。我们还回顾了血液系统恶性肿瘤形成的已知类型的粘附物,并推测它们与 EMT 表型的可能联系。我们假设,了解 EMT 相关粘附物的结构和调节将导致发现新的治疗干预措施,以克服疾病进展和对治疗的耐药性。