Deregulation of c-myc gene expression in human colon carcinoma is not accompanied by amplification or rearrangement of the gene
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Published in: | Molecular and Cellular Biology Vol. 5; no. 8; pp. 1969 - 1976 |
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AbstractList | The structure and expression of the c-myc oncogene were examined in 29 primary human colon adenocarcinomas. Dot blot hybridization of total RNA showed that 21 tumors (72%) had considerably elevated expression of c-myc (5- to 40-fold) relative to normal colonic mucosa. These data were corroborated by Northern blots of polyadenylated RNA, which showed a 2.3-kilobase transcript. Southern analysis of the c-myc locus in these tumors indicated the absence of amplification or DNA rearrangement in a 35-kilobase region encompassing the gene. In a parallel study, elevated expression of c-myc without amplification or DNA rearrangement was also observed in three of six colon carcinoma cell lines examined; in addition, unlike a normal colon cell line control, these three cell lines exhibited constitutive, high-level expression of the gene during their growth in cultures. These results indicate that elevated expression of the c-myc oncogene occurs frequently in primary human colon carcinomas and that the mechanism involved in the regulation of c-myc expression is altered in tumor-derived cell lines. Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue MCB About MCB Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy MCB RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0270-7306 Online ISSN: 1098-5549 Copyright © 2014 by the American Society for Microbiology. For an alternate route to MCB .asm.org, visit: MCB The structure and expression of the c-myc oncogene were examined in 29 primary human colon adenocarcinomas. Dot blot hybridization of total RNA showed that 21 tumors had considerably elevated expression of c-myc (5- to 40-fold) relative to normal colonic mucosa. These data were corroborated by Northern blots of polyadenylated RNA, which showed a 2.3-kilobase transcript. Southern analysis of the c-myc locus in these tumors indicated the absence of amplification or DNA rearrangement in a 35-kilobase region encompassing the gene. In a parallel study, elevated expression of c-myc without amplification or DNA rearrangement was also observed in three of six colon carcinoma cell lines examined. The results indicate that elevated expression of the c-myc oncogene occurs frequently in primary human colon carcinomas and that the mechanism invloved in the regulation of c-myc expression is altered in tumor-derived cell lines. |
Author | S M Astrin M D Erisman R E Diehl C C Morse P G Rothberg J M Spandorfer |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/3837853$$D View this record in MEDLINE/PubMed |
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Mendeley... The structure and expression of the c-myc oncogene were examined in 29 primary human colon adenocarcinomas. Dot blot hybridization of total RNA showed that 21... |
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StartPage | 1969 |
SubjectTerms | Cell Line Cells, Cultured Colon - metabolism Colonic Neoplasms - genetics Gene Amplification Genes, Regulator Humans Nucleic Acid Hybridization Oncogenes RNA, Neoplasm - isolation & purification Transcription, Genetic |
Title | Deregulation of c-myc gene expression in human colon carcinoma is not accompanied by amplification or rearrangement of the gene |
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