Department of Internal Medicine IV, University Heidelberg Hospital, Heidelberg, Germany.
Exp Dermatol. 2009 Dec;18(12):1067-9. doi: 10.1111/j.1600-0625.2009.00888.x.
Epithelial mesenchymal transition (EMT) has been implicated in neoplastic invasion and metastasis. We have previously generated six cell lines from human gingival mucosal keratinocytes immortalized by E6/E7 of human papillomavirus type 16. Ldk and NuB1 lines represented EMT phenotype and other four lines represented cobblestone non-EMT phenotype. These cell lines were utilized as model cells to determine whether inhibitors of apoptosis proteins and cell-cycle regulators were molecular players during EMT. EMT cells exhibited increased expression of vimentin, vascular endothelial growth factor (VEGF) receptor1 and the ability to form tubules on Matrigel as well as to grow anchorage independently. We found that EMT cells expressed significantly elevated levels of cIAP-1, Bclx and p27(kip) higher than non-EMT cells. These proteins could therefore be used as intrinsic indicators of EMT of human gingival keratinocytes.
上皮间质转化(EMT)与肿瘤的侵袭和转移有关。我们先前从 HPV16 的 E6/E7 永生化的人牙龈黏膜角质形成细胞中生成了 6 株细胞系。Ldk 和 NuB1 系代表 EMT 表型,其他 4 系代表鹅卵石样非 EMT 表型。这些细胞系被用作模型细胞,以确定凋亡蛋白抑制剂和细胞周期调节剂是否是 EMT 过程中的分子参与者。EMT 细胞表现出波形蛋白、血管内皮生长因子受体 1(VEGF 受体 1)的表达增加,以及在 Matrigel 上形成小管和锚定独立生长的能力。我们发现 EMT 细胞表达的 cIAP-1、Bclx 和 p27(kip)水平显著高于非 EMT 细胞。因此,这些蛋白可作为人牙龈角质形成细胞 EMT 的内在标志物。