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Merck

A preclinical xenograft model of prostate cancer using human tumors.

Nature protocols (2013-04-06)
Mitchell G Lawrence, Renea A Taylor, Roxanne Toivanen, John Pedersen, Sam Norden, David W Pook, Mark Frydenberg, Melissa M Papargiris, Birunthi Niranjan, Michelle G Richards, Hong Wang, Anne T Collins, Norman J Maitland, Gail P Risbridger
ABSTRAKT

Most cases of prostate cancer are now diagnosed as moderate-grade localized disease. These tumor specimens are important tools in the discovery and translation of prostate cancer research; however, unlike more advanced tumors, they are notoriously difficult to grow in the laboratory. We developed a system for efficiently xenografting localized human prostate cancer tissue, and we adapted this protocol to study the interactions between the specific subsets of epithelial and stromal cells. Fresh prostate tissues or isolated epithelial cells are recombined with mouse seminal vesicle mesenchyme (SVM) and grafted under the renal capsule of immunodeficient mice for optimum growth and survival. Alternatively, mouse mesenchyme can be replaced with human prostate fibroblasts in order to determine their contribution to tumor progression. Grafts can be grown for several months to determine the effectiveness of novel therapeutic compounds when administered to host mice, thereby paving the way for personalizing the treatment of individual prostate cancers.

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Sigma-Aldrich
Hyaluronidase from sheep testes, Type II, lyophilized powder, ≥300 units/mg solid
Sigma-Aldrich
Bovine Serum Albumin, heat shock fraction, pH 7, ≥98%
Sigma-Aldrich
Collagenase from Clostridium histolyticum, for general use, Type I, ≥125 CDU/mg solid
Sigma-Aldrich
Anti-Androgen Receptor antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution