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PMID: 1394214 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Distribution of cells expressing myc proteins in human colorectal epithelium, polyps, and malignant tumors.

Cancer research ·Vol. 52 ·No. 21 ·1992-11-01 ·Pages 5853-64

Melhem MF, Meisler AI, Finley GG, Bryce WH, Jones MO, Tribby II, Pipas JM, Koski RA

Abstract

The myc gene family encodes nuclear phosphoproteins that are thought to play a role in the control of cellular proliferation and differentiation. We have undertaken an immunohistochemical study assessing the expression of myc gene family proteins in individual cells of normal colonic mucosa, colorectal polyps, and colorectal adenocarcinomas. We screened a panel of mouse monoclonal antibodies that we raised against recombinant human c-myc and N-myc proteins for recognition of myc proteins in paraffin tissue sections. Two of these antibodies, H120C69 and H8C150, were selected for indirect immunoperoxidase staining of tissue sections from 16 normal mucosas, 24 polyps, and 30 adenocarcinomas. In normal colon, about 25% of the cells in the lower one-third of the crypts of Lieberkühn stain for myc-related protein. This distribution resembles that of proliferating cells in the crypt. Benign hyperplastic polyps resemble normal mucosa in their myc staining pattern, with about 25% of the cells positive. In adenomatous polyps, the putative precursors of adenocarcinomas, from 50 to 100% of the cells stain positively for myc protein. In these cases, stained cells extend to the luminal surface, consistent with the previously reported expansion of the proliferation zone in these lesions. All adenocarcinomas examined had increased levels of myc protein relative to normal mucosa. The tumor cells exhibited markedly heterogeneous myc staining patterns, both among different tumors and, in some cases, within a single tumor. Comparison with Ki-67 monoclonal antibody staining indicates that myc protein expression in many tumors is uncoupled from cellular proliferation. Surprisingly, we observed increased numbers of myc-expressing cells and increased levels of myc protein in histologically normal colon directly adjacent to tumor, suggesting that many colorectal carcinomas secrete growth factors that activate gene expression in neighboring normal mucosa.

MeSH Terms
Adenocarcinoma/chemistry,pathology Antibodies, Monoclonal Antibody Specificity Cell Nucleus/chemistry Colon/chemistry,cytology,pathology Colonic Neoplasms/chemistry,pathology Colonic Polyps/chemistry,pathology Cytosol/chemistry Frozen Sections Humans Hyperplasia Immunohistochemistry Intestinal Mucosa/chemistry,cytology Ki-67 Antigen Nuclear Proteins/analysis Paraffin Embedding Proto-Oncogene Proteins c-myc/analysis RNA, Messenger/analysis Tumor Cells, Cultured
Chemicals
Antibodies, Monoclonal Ki-67 Antigen Nuclear Proteins Proto-Oncogene Proteins c-myc RNA, Messenger
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Melhem M F
Department of Pathology, University of Pittsburgh School of Medicine, Pennsylvania 15260.
Meisler A I
Finley G G
Bryce W H
Jones M O
Tribby I I
Pipas J M
Koski R A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1992-11-01
Pages
5853-64
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · CA46547 · United States
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