Enhanced tumor growth of both primary and established human and murine tumor cells in athymic mice after coinjection with Matrigel. 1991

R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
Laboratory of Developmental Biology, National Institute of Dental Research, National Institutes of Health, Bethesda, MD 20892.

Previously we found that the reconstituted basement membrane matrix Matrigel, when premixed with human small-cell lung carcinoma cells and injected subcutaneously into athymic mice, permitted tumor growth, whereas cells injected in the absence of Matrigel did not form tumors. In the present study, we examined additional cell types and determined some of the underlying mechanisms involved in the promotion of tumor formation by Matrigel. The tumor cell lines that we studied included transformed mouse Englebreth-Holm-Swarm tumor cells (T-EHS), human submandibular carcinoma A253 cells, mouse melanoma B16F10 cells, human epidermoid carcinoma KB cells, and human primary renal cell carcinoma cells. When coinjected subcutaneously with Matrigel, these cell lines formed rapidly proliferating tumors. Primary biopsy specimens of human colon carcinoma, when dispersed and coinjected with Matrigel, also formed tumors. Only A253, KB, and B16F10 cells formed small tumors in the absence of Martrigel, but a fivefold to tenfold increase in tumor size was observed in the presence of Matrigel. These data demonstrate a useful method for improving the growth of human tumors in athymic mice.

UI MeSH Term Description Entries
D007797 Laminin Large, noncollagenous glycoprotein with antigenic properties. It is localized in the basement membrane lamina lucida and functions to bind epithelial cells to the basement membrane. Evidence suggests that the protein plays a role in tumor invasion. Merosin,Glycoprotein GP-2,Laminin M,Laminin M Chain,Chain, Laminin M,Glycoprotein GP 2,M Chain, Laminin
D008810 Mice, Inbred C57BL One of the first INBRED MOUSE STRAINS to be sequenced. This strain is commonly used as genetic background for transgenic mouse models. Refractory to many tumors, this strain is also preferred model for studying role of genetic variations in development of diseases. Mice, C57BL,Mouse, C57BL,Mouse, Inbred C57BL,C57BL Mice,C57BL Mice, Inbred,C57BL Mouse,C57BL Mouse, Inbred,Inbred C57BL Mice,Inbred C57BL Mouse
D008819 Mice, Nude Mutant mice homozygous for the recessive gene "nude" which fail to develop a thymus. They are useful in tumor studies and studies on immune responses. Athymic Mice,Mice, Athymic,Nude Mice,Mouse, Athymic,Mouse, Nude,Athymic Mouse,Nude Mouse
D009368 Neoplasm Transplantation Experimental transplantation of neoplasms in laboratory animals for research purposes. Transplantation, Neoplasm,Neoplasm Transplantations,Transplantations, Neoplasm
D009374 Neoplasms, Experimental Experimentally induced new abnormal growth of TISSUES in animals to provide models for studying human neoplasms. Experimental Neoplasms,Experimental Neoplasm,Neoplasm, Experimental
D011509 Proteoglycans Glycoproteins which have a very high polysaccharide content. Proteoglycan,Proteoglycan Type H
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D003094 Collagen A polypeptide substance comprising about one third of the total protein in mammalian organisms. It is the main constituent of SKIN; CONNECTIVE TISSUE; and the organic substance of bones (BONE AND BONES) and teeth (TOOTH). Avicon,Avitene,Collagen Felt,Collagen Fleece,Collagenfleece,Collastat,Dermodress,Microfibril Collagen Hemostat,Pangen,Zyderm,alpha-Collagen,Collagen Hemostat, Microfibril,alpha Collagen
D004338 Drug Combinations Single preparations containing two or more active agents, for the purpose of their concurrent administration as a fixed dose mixture. Drug Combination,Combination, Drug,Combinations, Drug
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
January 1993, Breast cancer research and treatment,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
October 1991, Journal of the National Cancer Institute,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
January 1998, Neurosurgery,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
January 1985, Experimental cell biology,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
October 1986, Histology and histopathology,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
October 1978, Cancer research,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
December 2005, Clinical cancer research : an official journal of the American Association for Cancer Research,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
July 1986, International journal of cancer,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
March 1984, Cancer research,
R Fridman, and M C Kibbey, and L S Royce, and M Zain, and M Sweeney, and D L Jicha, and J R Yannelli, and G R Martin, and H K Kleinman
September 1997, The Anatomical record,
Copied contents to your clipboard!