Abstract
We compared the cytogenetic pattern of 20 different primary tumor cell cultures (PTCC) of renal cell carcinoma (RCC) to their cytokine secretion and oncogene expression. High secretion of IL-6 (gene locus on chromosome 7p21-p14) was correlated with the gain of an additional chromosome 7. Structural changes involving chromosome 5q22, the site of the GM-CSF gene, were matched with the high secretion of GM-CSF in PTCC. No such association was found for beta 2-microglobulin, TGF-beta 1, TNF-alpha, IL-8, and oncogenes, such as c-fos, c-myc, and pan-ras. Our approach may be useful in simultaneously analyzing several factors contributing to tumor progression and may contribute to understanding the multistep development of RCC.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Carcinoma, Renal Cell / genetics
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Carcinoma, Renal Cell / metabolism*
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Cytokines / biosynthesis*
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Cytokines / genetics
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Drug Resistance, Multiple
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Drug Resistance, Neoplasm
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Epidermal Growth Factor / biosynthesis
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Female
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Gene Expression Regulation, Neoplastic*
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Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis
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HSP70 Heat-Shock Proteins / biosynthesis
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Humans
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Intercellular Adhesion Molecule-1 / biosynthesis
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Interleukins / biosynthesis
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Male
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Middle Aged
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Proto-Oncogenes* / genetics
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Transforming Growth Factor alpha / biosynthesis
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Tumor Cells, Cultured
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Tumor Necrosis Factor-alpha / biosynthesis
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Tumor Suppressor Protein p53 / biosynthesis
Substances
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Cytokines
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HSP70 Heat-Shock Proteins
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Interleukins
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Transforming Growth Factor alpha
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Tumor Necrosis Factor-alpha
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Tumor Suppressor Protein p53
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Intercellular Adhesion Molecule-1
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Epidermal Growth Factor
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Granulocyte-Macrophage Colony-Stimulating Factor