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FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex

机译:FBXO31是染色体16q24.3衰老基因,候选乳腺肿瘤抑制因子和sCF复合物的组成部分

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摘要

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 G2 to early G1 phase. Ectopic expression of FBXO31 in the breast cancer cell line MDA-MB-468 resulted in the accumulation of cells at the G1 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 SCFFBXO31 complexes that target particular substrates, critical for the normal execution of the cell cycle, for ubiquitination and subsequent degradation. (Cancer Res 2005; 65(24): 11304-313)
机译:先前显示,位于16q24.3乳腺癌杂合性缺失区域的BAC在转移至乳腺癌细胞系后可恢复细胞衰老。我们已经显示,FBXO31尽管位于该BAC的远端,但可以在乳腺癌细胞系MCF-7中诱导细胞衰老,并且可能是候选的衰老基因。 FBXO31具有与肿瘤抑制物一致的特性,因为在两种乳腺癌细胞系中FBXO31的异位表达抑制了塑料上的集落生长,并抑制了MCF-7细胞系中的细胞增殖。此外,与正常乳腺中的相对表达相比,乳腺肿瘤细胞系和原发性肿瘤中FBXO31的水平下调。 FBXO31在乳腺癌细胞系MCF-10A和SKBR3中受到细胞周期调控,从G2晚期到G1早期达到最大表达。 FBXO31在乳腺癌细胞系MDA-MB-468中的异位表达导致细胞周期G1期的细胞蓄积。 FBXO31包含一个F-box域,并与蛋白Skp1,Roc-1和Cullin-1相关,这表明FBXO31是SCF泛素化复合体的一个组成部分。我们提出,FBXO31通过产生靶向特定底物的SCFFBXO31复合物而起肿瘤抑制作用,这对于细胞周期的正常执行,泛素化和随后的降解至关重要。 (Cancer Res 2005; 65(24):11304-313)

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