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Deletion, Mutation, and Loss of Expression of KLF6 in Human Prostate Cancer

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2003 Mar 26
PMID 12651626
Citations 50
Authors
Affiliations
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Abstract

Kruppel-like factors (KLFs) are a group of transcription factors that appear to be involved in different biological processes including carcinogenesis. In a recent study, KLF6 was reported as a tumor suppressor gene in prostate cancer because of its frequent loss of heterozygosity (LOH) and mutation as well as functional suppression of cell proliferation. Loss of chromosomal locus spanning KLF6 is relatively infrequent in other published studies of prostate cancer, however. To clarify the role of KLF6 in prostate cancers, particularly those that are high grade, we examined KLF6 for deletion, mutation, and loss of expression in 96 prostate cancer samples including 21 xenografts/cell lines. Loss of heterozygosity occurred in 4 (19%) of 21 xenografts/cell lines and 8 (28%) of 29 informative tumors. Fourteen of the 96 (15%) samples showed 15 somatic sequence changes in the KLF6 gene, including 7 that changed KLF6 peptide sequences, 4 that did not, and 4 that were located in untranslated regions. Expression levels of KLF6 were significantly lost in 4 of 20 (20%) xenografts/cell lines of prostate cancer, as detected by RT-PCR and Northern blot analysis. These findings indicate that significant genetic alterations of KLF6 occur in a minority of high-grade prostate cancers.

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References
1.
Murakami Y, Albertsen H, Brothman A, Leach R, White R . Suppression of the malignant phenotype of human prostate cancer cell line PPC-1 by introduction of normal fragments of human chromosome 10. Cancer Res. 1996; 56(9):2157-60. View

2.
Ittmann M . Allelic loss on chromosome 10 in prostate adenocarcinoma. Cancer Res. 1996; 56(9):2143-7. View

3.
Komiya A, Suzuki H, Ueda T, Yatani R, Emi M, Ito H . Allelic losses at loci on chromosome 10 are associated with metastasis and progression of human prostate cancer. Genes Chromosomes Cancer. 1996; 17(4):245-53. DOI: 10.1002/(SICI)1098-2264(199612)17:4<245::AID-GCC6>3.0.CO;2-3. View

4.
Subramaniam M, Hefferan T, Tau K, Peus D, Pittelkow M, Jalal S . Tissue, cell type, and breast cancer stage-specific expression of a TGF-beta inducible early transcription factor gene. J Cell Biochem. 1998; 68(2):226-36. View

5.
Whang Y, Wu X, Suzuki H, Reiter R, Tran C, Vessella R . Inactivation of the tumor suppressor PTEN/MMAC1 in advanced human prostate cancer through loss of expression. Proc Natl Acad Sci U S A. 1998; 95(9):5246-50. PMC: 20246. DOI: 10.1073/pnas.95.9.5246. View