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Cancer Res ; 65(24): 11304-13, 2005 Dec 15.
Article in English | MEDLINE | ID: mdl-16357137

ABSTRACT

A BAC located in the 16q24.3 breast cancer loss of heterozygosity region was previously shown to restore cellular senescence when transferred into breast tumor cell lines. We have shown that FBXO31, although located just distal to this BAC, can induce cellular senescence in the breast cancer cell line MCF-7 and is the likely candidate senescence gene. FBXO31 has properties consistent with a tumor suppressor, because ectopic expression of FBXO31 in two breast cancer cell lines inhibited colony growth on plastic and inhibited cell proliferation in the MCF-7 cell line. In addition, compared with the relative expression in normal breast, levels of FBXO31 were down-regulated in breast tumor cell lines and primary tumors. FBXO31 was cell cycle regulated in the breast cell lines MCF-10A and SKBR3 with maximal expression from late G(2) to early G(1) phase. Ectopic expression of FBXO31 in the breast cancer cell line MDA-MB-468 resulted in the accumulation of cells at the G(1) phase of the cell cycle. FBXO31 contains an F-box domain and is associated with the proteins Skp1, Roc-1, and Cullin-1, suggesting that FBXO31 is a component of a SCF ubiquitination complex. We propose that FBXO31 functions as a tumor suppressor by generating SCF(FBXO31) complexes that target particular substrates, critical for the normal execution of the cell cycle, for ubiquitination and subsequent degradation.


Subject(s)
Breast Neoplasms/genetics , Cellular Senescence/genetics , Chromosomes, Human, Pair 16 , F-Box Proteins/genetics , Genes, Tumor Suppressor , Tumor Suppressor Proteins/genetics , Blotting, Northern , Breast Neoplasms/metabolism , Carrier Proteins/metabolism , Cell Cycle Proteins/metabolism , Cell Proliferation , Chromosomes, Artificial, Bacterial , Colony-Forming Units Assay , Cullin Proteins/metabolism , F-Box Proteins/metabolism , Female , G1 Phase , G2 Phase , Humans , Immunoprecipitation , Kidney/metabolism , Tumor Cells, Cultured , Tumor Suppressor Proteins/metabolism
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