Vatne V, Fjellbirkeland L, Litlekalsoey J, Hoestmark J
Department of Surgery, Haukeland Hospital, University of Bergen, Norway.
Anticancer Res. 1998 Nov-Dec;18(6A):3985-9.
To study invasion of transitional cell cancer three-dimensional coculture assay consisting of living human tissues has been developed. Multicellular spheroids initiated from an invasive human bladder tumour cell line (Hu-1703He) were confronted with precultured fragments derived from normal human bladder mucosa. The fragments consisted of a surface epithelium and a central stroma. An intact epithelium prevented adhesion of the tumour cells to the fragments. By removing the surface epithelium prior to confrontation, tumour cells rapidly adhered to, migrated on and invaded the bladder fragments. This process was demonstrated by an inverted confocal laser scanning microscope on live tissue pre-incubated with fluorescent dyes. The coculture model enables the study of factors regulating different steps of tumour invasion in human bladder.
为研究移行细胞癌的侵袭,已开发出一种由活人组织构成的三维共培养检测方法。从侵袭性人膀胱肿瘤细胞系(Hu-1703He)起始形成的多细胞球体,与源自正常人膀胱黏膜的预培养片段相互作用。这些片段由表面上皮和中央基质组成。完整的上皮可阻止肿瘤细胞黏附于片段。在相互作用前去除表面上皮,肿瘤细胞会迅速黏附、迁移并侵袭膀胱片段。这一过程通过倒置共聚焦激光扫描显微镜在预先用荧光染料孵育的活组织上得以证实。该共培养模型有助于研究调控人膀胱肿瘤侵袭不同步骤的因素。