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Cytogenetic Studies of Tumor Tissue from Patients with Nonfamilial Renal Cell Carcinoma

TLDR
The results suggest that renal cell carcinoma may be cytogenetically classified into 3 categories: tumors with changes of chromosome 3: (b) tumors with other clonal aberrations; and (c) tumors without clonal changes.
Abstract
A method combining an enzymatic technique and short term culture was applied to 27 tumor tissues from 22 patients with nonfamilial renal cell carcinoma in order to establish the chromosome changes in these tumors. Chromosome analyses were successfully carried out in quinacrine mustard-Hoechst 33258 and G-banded preparations of 14 tumors from 12 patients, including 2 cases in which established cell lines were obtained after 43 and 64 days in culture and maintained for 25 and 30 passages in an in vitro system, respectively. The modal chromosome numbers ranged from 38–46 in 11 samples, involving chromosomes in structural and numerical changes and 72 chromosomes in one case, with the remaining 2 samples showing a variety of chromosome numbers. Banding analysis revealed 45 clonal aberrations in 11 tumor samples from 10 patients and nonclonal aberrations in the remaining 3 samples from 2 of the patients. Rearrangements of chromosome 3 were observed in 12 tumors, with the breakpoints on this chromosome almost totally clustered from p11 to p21. In one case both primary and metastatic tumors were studied, and an isochromosome for the long arm of chromosome 1 was observed as clonal in origin in the metastatic tissue. Two cases showed nonclonal changes. The remaining case had one clonal abnormality, i.e. , deletion of 6q. Of the remaining 33 clones, chromosomes 1, 2, 6, 11, and 17 were frequently involved. These results suggest that renal cell carcinoma may be cytogenetically classified into 3 categories: ( a ) tumors with changes of chromosome 3; ( b ) tumors with other clonal aberrations; and ( c ) tumors without clonal changes. Rearrangements of chromosome 3 may be possibly associated with the genesis and/or progression of renal cell carcinoma.

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Journal ArticleDOI

Chromosome aberrations and cancer

TL;DR: The association of consistent chromosome aberrations with particular types of cancer has led to the identification of some of these genes and the elucidation of their mechanisms of action.
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The Approaching Era of the Tumor Suppressor Genes

TL;DR: Tumor suppressor genes will probably turn out to be as, if not more, diversified as the oncogenes and consideration of both kinds of genes may reveal common or interrelated functional properties.
Book ChapterDOI

Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes

TL;DR: Though hMLH1 plays an obvious role in the development of specific mismatch repair-deficient cancers, it cannot revert the tumor phenotype and therefore cannot be considered a proper tumor suppressor, and this review discusses the methodological advantages and limitations of the various approaches.
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Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer.

W. M. Linehan, +2 more
- 15 Feb 1995 - 
TL;DR: There is an increased incidence of renal cancer among workers exposed to asbestos and among leather workers, 4,5 and a strong correlation has been found with cigarette smoking.
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Cytogenetics of papillary renal cell tumors

TL;DR: Chromosome aberrations were determined in short‐term cultures of 18 papillary renal cell tumors, as well as in the cell line ACHN, and the results were evaluated together with previously published cases and found that chromosomes 7, 17, and 16 and the Y chromosome were specifically involved in the karyotype changes in this tumor type.
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