Department of Colorectal Surgery, The Royal Marsden Hospital, London, UK.
Surg Oncol. 2012 Dec;21(4):316-23. doi: 10.1016/j.suronc.2012.08.003. Epub 2012 Sep 14.
Epithelial mesenchymal transition (EMT) may be physiological as part of embryological development, or pathological as part of cancer development. It is one of the key initiating events in the metastatic cascade. EMT has profound effects on tumour cell invasiveness, proliferation and motility. In the present article we aimed to review the potential role of EMT as a process to explain colorectal cancer progression and resistance to neoadjuvant therapy.
Extensive literature searches were performed in Pubmed, EMBASE and Google Scholar databases to identify relevant articles published before March 2012.
There is adequate evidence to support the complex upstream signalling alterations needed for EMT to occur in colorectal cancers. Changes of EMT are likely to be found at the tumour invasive front: the deepest, growing tumour margin. Loss of E-cadherin at the cell membrane causes loss of cellular integrity, with subsequent migration of malignant cells and tumour budding. These processes are associated with metastases and recurrence of colorectal cancer. There is early evidence from a limited number of studies that resistance to neoadjuvant therapy in colorectal cancer is associated with changes of EMT. However, there is a lack of supporting evidence originating from human colorectal cancer tissues.
Emerging evidence demonstrates that development of EMT in colorectal cancer leads to an aggressive phenotype that may promote metastatic spread, and augment treatment resistance during neoadjuvant therapy. A clearer understanding of the processes and role of EMT in colorectal cancer may also highlight novel therapeutic strategies.
上皮间质转化(EMT)可能是胚胎发育过程中的生理现象,也可能是癌症发展过程中的病理现象。它是转移级联过程中的关键起始事件之一。EMT 对肿瘤细胞的侵袭性、增殖和运动性有深远的影响。在本文中,我们旨在综述 EMT 作为一种解释结直肠癌进展和对新辅助治疗耐药的过程的潜在作用。
在 Pubmed、EMBASE 和 Google Scholar 数据库中进行了广泛的文献检索,以确定 2012 年 3 月前发表的相关文章。
有充分的证据支持 EMT 在结直肠癌中发生所需的复杂上游信号改变。EMT 的变化可能发生在肿瘤侵袭前沿:最深、生长最快的肿瘤边缘。细胞膜上 E-钙黏蛋白的丢失导致细胞完整性丧失,随后恶性细胞迁移和肿瘤芽生。这些过程与结直肠癌的转移和复发有关。有早期证据表明,结直肠癌对新辅助治疗的耐药性与 EMT 的改变有关。然而,缺乏来自人类结直肠癌组织的支持证据。
新出现的证据表明,结直肠癌中 EMT 的发展导致了侵袭性表型,可能促进转移扩散,并在新辅助治疗期间增强治疗耐药性。更清楚地了解 EMT 在结直肠癌中的过程和作用,也可能突出新的治疗策略。