Carsberg C J, Myers K A, Stern P L
CRC Department of Immunology, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.
Int J Cancer. 1996 Sep 27;68(1):84-92. doi: 10.1002/(SICI)1097-0215(19960927)68:1<84::AID-IJC15>3.0.CO;2-6.
The 5T4 antigen is defined by a monoclonal antibody (MAb) specific for human trophoblast. It is also expressed by many types of tumour cell and has been associated with metastasis and poor clinical outcome in a number of cancers. This pattern of expression is consistent with a mechanistic involvement of 5T4 molecules in the spread of cancer cells. The 5T4 antigen is a transmembrane glycoprotein with a 310 amino acid extracellular domain and a 44 amino acid cytoplasmic domain. Transfection of full-length 5T4 cDNA into epithelial cells alters cell-cell contacts and cellular motility. Thus, in 5T4-transfected CL-S1 murine mammary cells, 5T4 expression is associated with dendritic morphology, accompanied by abrogation of actin/cadherin-containing contacts and increased motility. In transfected MDCK canine kidney epithelial cells, 5T4 over-expression also results in increased motility, but disruption of cell-cell contacts, either by culturing cells in low calcium medium or by addition of HGF/SF, is needed. The effects of 5T4 expression on morphology and motility are separable since cells transfected with a truncated form of 5T4 cDNA in which the cytoplasmic domain is deleted reveal that the latter is necessary to abrogate actin/cadherin-containing contacts but does not influence the effects on motility. Thus, 5T4 molecules can deliver signals through both the extracellular and intracellular domains, and the resultant effects are consistent with a role for 5T4 molecules in invasion processes.
5T4抗原由一种针对人类滋养层细胞的单克隆抗体(MAb)所定义。它也在多种肿瘤细胞中表达,并且在多种癌症中与转移及不良临床预后相关。这种表达模式与5T4分子在癌细胞扩散过程中的机制性参与相一致。5T4抗原是一种跨膜糖蛋白,具有一个含310个氨基酸的细胞外结构域和一个含44个氨基酸的细胞质结构域。将全长5T4 cDNA转染到上皮细胞中会改变细胞间接触和细胞运动性。因此,在转染了5T4的CL-S1小鼠乳腺细胞中,5T4的表达与树突状形态相关,伴随着含肌动蛋白/钙黏着蛋白接触的消除和运动性增加。在转染的MDCK犬肾上皮细胞中,5T4的过表达也会导致运动性增加,但需要通过在低钙培养基中培养细胞或添加HGF/SF来破坏细胞间接触。5T4表达对形态和运动性的影响是可分离的,因为用缺失细胞质结构域的5T4 cDNA截短形式转染的细胞表明,后者对于消除含肌动蛋白/钙黏着蛋白的接触是必需但不影响对运动性的作用。因此,5T4分子可以通过细胞外和细胞内结构域传递信号,并且产生的效应与5T4分子在侵袭过程中的作用一致。