| Literature DB >> 2322116 |
G D Steele1, S Davis, H Yow, J M Wong, E N Rivers, I C Summerhayes, T S Ravikumar, L B Chen.
Abstract
Alterations in gene expression associated with colorectal cancer have been difficult to study because mucosal cell progenitors are not available in culture. We therefore examined specific genes in approximately 100 human colon cancer cell lines using complementary DNA probes and found profound alterations and heterogenity of gene expression in human colorectal carcinoma. Our data imply that understanding human colorectal cancer will not be accomplished by studying one or two oncogenes in a limited number of cell lines or fresh human tissue. More appropriate postulates of transformation to dictate experimental design may include the investigation of proposed three-dimensional structural changes of interface chromatin or other generalized structural relationships that could predispose to an aberrant gene expression program during transformation. Furthermore, focusing on mechanisms of initiation and defining the molecular genetic markers of gastrointestinal mucosal initiation should lead to a more focused set of genetic, rather than epigenetic, mechanisms that underlie oncogenic transformation.Entities:
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Year: 1990 PMID: 2322116 DOI: 10.1001/archsurg.1990.01410160079018
Source DB: PubMed Journal: Arch Surg ISSN: 0004-0010