The overall aim of this research is to identify and characterize four classes of genes involved in multistage carcinogenesis. The first class includes genes associated with susceptibility to tumor promoter-induced neoplastic transformation. The second class includes genes that specify expression of tumor cell phenotype. The third class is tumor suppressor genes, and the fourth, apoptosis-causing genes. Mouse JB6 promotion-resistant (P-), promotion-sensitive (P+), and tumorigenic (Tx) JB6-derived epidermal cell lines have been found to differ in the expression or activity of several susceptibility-related genes described in the accompanying project, Z01CP05383-12 LVC, """"""""Membrane Signal Transduction in Tumor Promotion."""""""" Human nasopharyngeal carcinomas (NPCs) from China show a heterozygous expressed mutation in codon 280 of the tumor suppressor gene, p53. The novel mutated p53 has oncogenic activity and functions dominantly in the presence of wild-type p53 to inhibit transcriptional activation and to cause progression toward neoplastic phenotype in two models. Since a high proportion of human NPCs and tumorigenic mouse JB6 cells express only wild-type p53, we have inquired as to whether events downstream of p53 might be inactivated, thus losing p53-dependent tumor suppressor activity as if a p53 mutation had occurred. WAF-1/CIP-1, a gene transcriptionally controlled by p53 that regulates complexes involved in the G1 checkpoint, has been found not to be mutated in NPC or in JB6 tumor cells. A codon 31 polymorphism in WAF-1 has been found, however, that offers utility for following allele distribution in Chinese populations. A new candidate tumor suppressor gene has been identified by the differential mRNA display technique applied to the mouse JB6 P- to P+ to Tx progression series. This gene, identified as tissue inhibitor of metalloproteinase-3 (TIMP-3), is expressed in preneoplastic, but not neoplastic (Tx), JB6 cells. When expressed in colon carcinoma cells that lack it, TIMP-3 suppresses carcinoma growth in nude mice and produces G1 arrest.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CP005382-12
Application #
5201480
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Division of Cancer Epidemiology and Genetics
Department
Type
DUNS #
City
State
Country
United States
Zip Code