Brzozowa Marlena, Michalski Marek, Wyrobiec Grzegorz, Piecuch Adam, Dittfeld Anna, Harabin-Słowińska Marzena, Boroń Dariusz, Wojnicz Romuald
Chair and Department of Histology and Embryology, Faculty of Medicine and Dentistry in Zabrze, Medical University of Silesia, Katowice, Poland.
Contemp Oncol (Pozn). 2015;19(4):265-70. doi: 10.5114/wo.2014.42173. Epub 2015 Sep 28.
Snail1 is a zinc-finger transcription factor, which plays a role in colorectal cancer development by silencing E-cadherin expression and inducing epithelialmesenchymal transition (EMT). During EMT tumour cells acquire a mesenchymal phenotype that is responsible for their invasive activities. Consequently, Snail1 expression in colorectal cancer is usually associated with progression and metastasis. Some studies revealed that about 77% of colon cancer samples display Snail1 immunoreactivity both in activated fibroblasts and in carcinoma cells that have undergone EMT. Therefore, expression of this factor in the stroma may indicate how many cells possess the abilities to escape from the primary tumour mass, invade the basal lamina and colonise distant target organs. Blocking snail proteins activity has the potential to avert cancer cell metastasis by interfering with such cellular processes as remodelling of the actin cytoskeleton, migration and invasion, which are clearly associated with the aggressive phenotype of the disease. Moreover, the link between factors from the snail family and cancer stem cells suggests that inhibitory agents may also prove their potency as inhibitors of cancer recurrence.
Snail1是一种锌指转录因子,它通过使E-钙黏蛋白表达沉默并诱导上皮-间质转化(EMT),在结直肠癌发展过程中发挥作用。在EMT过程中,肿瘤细胞获得一种间质表型,这种表型与其侵袭活性有关。因此,Snail1在结直肠癌中的表达通常与进展和转移相关。一些研究表明,约77%的结肠癌样本在活化的成纤维细胞和经历EMT的癌细胞中均显示Snail1免疫反应性。因此,该因子在基质中的表达可能表明有多少细胞具备逃离原发肿瘤块、侵入基底膜并在远处靶器官定植的能力。阻断蜗牛蛋白的活性有可能通过干扰诸如肌动蛋白细胞骨架重塑、迁移和侵袭等细胞过程来避免癌细胞转移,这些过程显然与该疾病的侵袭性表型相关。此外,蜗牛家族因子与癌症干细胞之间的联系表明,抑制剂也可能证明其作为癌症复发抑制剂的效力。