Journal
AMERICAN JOURNAL OF PATHOLOGY
Volume 164, Issue 5, Pages 1607-1614Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/S0002-9440(10)63719-4
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Funding
- NCI NIH HHS [R01 CA094858, R01CA94858] Funding Source: Medline
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The homeodomain transcription factor Nkx3.l and the cyclin-dependent kinase inhibitor p27(kip1) have both been implicated in Prostate tumor suppression. In addition, both of these molecules demonstrate haploinsufficiency for tumor suppression, in which loss of a single allele is sufficient to lead to the development of preneoplastic or neoplastic lesions. We have generated mice carrying compound mutant alleles of Nkx3.1 and p27 to explore the roles of these factors in prostate tumorigenesis. Our results indicate that Nkx3.1 and p27(kip1) cooperate to suppress the proliferation of prostatic epithelial cells and the formation of preneoplastic lesions resembling prostatic intraepithelial neoplasia. Cooperativity was most evident with complete loss of at least one of the two genes because compound heterozygous mice exhibited a prostatic phenotype that was no more severe than that of single heterozygous mutants. Thus Nkx3.1 and P27(kip1) regulate prostatic epithelial cell proliferation and tumor initiation by affecting both haploinsufficient and nonhaploinsufficient pathways.
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