Human bladder tumor fragments were cultured on collagen gel. In this system, the three dimensional architecture, cell-to-stroma and cell-to-cell interactions, and tumor heterogeneity were maintained. Cell viability and labeling index (LI) were determined by exposure to 3H-thymidine and autoradiography. Of the samples from 20 patients with transitional cell carcinoma, 14 (70%) were successfully cultured and had a mean LI of 32%. In addition, one specimen from a patient with squamous cell carcinoma was cultured and had a LI of 61%. Cultured samples were tested for chemosensitivity using a two hour exposure of mitomycin C in concentrations ranging from one to 50 micrograms./ml. A dose-dependent relationship was demonstrated; LI decreased as mitomycin C concentrations increased. The methodology described provides an alternative to suspension or monolayer techniques of culturing human bladder tumors for pharmacological studies.
Andrew Shumaker, Miriam Harel, Jordan Gitlin, Steven C. Friedman, Lori Dyer, Jaime Freyle, Paul Zelkovic, Mark Horowitz, Ronnie Fine, Richard N. Schlussel
Jasper Mullenders, Evelien de Jongh, Anneta Brousali, Mieke Roosen, Jan P. A. Blom, Harry Begthel, Jeroen Korving, Trudy Jonges, Onno Kranenburg, Richard P. Meijer, Hans Clevers
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