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In situ detection of c-myc mRNA in adenocarcinomas, adenomas, and mucosa of human colon.

Abstract
We used a sensitive RNA:RNA in situ hybridization technique to study steady-state levels of c-myc proto-oncogene mRNA in primary human colon adenocarcinomas, villous adenomas, and normal mucosa samples. Frozen tissue sections, fixed in 4% buffered paraformaldehyde, were hybridized to 35S-labeled anti-sense transcripts of a c-myc clone and processed for autoradiography. The specificity of the hybridization was controlled by using 35S-labeled plasmid transcripts as a negative control, while RNA preservation in the tissue sample was assessed by using 35S-labeled anti-sense transcripts of a murine 28S rRNA clone. c-myc RNA was detectable in all the carcinomas (eight) and villous adenomas (four), but steady-state levels varied from high to low in different tumors with similar histology. Low levels of c-myc RNA were detected in epithelial stem cells of some of the normal mucosa samples (five). No genetic alterations of the c-myc locus were found by Southern analysis of DNAs extracted from the carcinomas.
AuthorsR Mariani-Costantini, C Theillet, P Hutzell, G Merlo, J Schlom, R Callahan
JournalThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (J Histochem Cytochem) Vol. 37 Issue 3 Pg. 293-8 (Mar 1989) ISSN: 0022-1554 [Print] United States
PMID2645359 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • DNA Probes
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-myc
  • RNA Probes
  • RNA, Messenger
Topics
  • Adenocarcinoma (analysis)
  • Adenoma (analysis)
  • Blotting, Northern
  • Colon (analysis)
  • Colonic Neoplasms (analysis)
  • DNA Probes
  • Humans
  • Intestinal Mucosa (analysis)
  • Nucleic Acid Hybridization
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins (genetics)
  • Proto-Oncogene Proteins c-myc
  • RNA Probes
  • RNA, Messenger (analysis)

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