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NF-κB 诱导激酶调节乳腺癌中的干细胞表型。

NF-kappaΒ-inducing kinase regulates stem cell phenotype in breast cancer.

机构信息

Instituto Nacional de Medicina Genómica (INMEGEN), México, 14610, México.

Unidad de Investigación Médica en Enfermedades Oncológicas (UIMEO), Hospital de Oncología IMSS, México.

出版信息

Sci Rep. 2016 Nov 23;6:37340. doi: 10.1038/srep37340.

Abstract

Breast cancer stem cells (BCSCs) overexpress components of the Nuclear factor-kappa B (NF-κB) signaling cascade and consequently display high NF-κB activity levels. Breast cancer cell lines with high proportion of CSCs exhibit high NF-κB-inducing kinase (NIK) expression. The role of NIK in the phenotype of cancer stem cell regulation is poorly understood. Expression of NIK was analyzed by quantitative RT-PCR in BCSCs. NIK levels were manipulated through transfection of specific shRNAs or an expression vector. The effect of NIK in the cancer stem cell properties was assessed by mammosphere formation, mice xenografts and stem markers expression. BCSCs expressed higher levels of NIK and its inhibition through small hairpin (shRNA), reduced the expression of CSC markers and impaired clonogenicity and tumorigenesis. Genome-wide expression analyses suggested that NIK acts on ERK1/2 pathway to exert its activity. In addition, forced expression of NIK increased the BCSC population and enhanced breast cancer cell tumorigenicity. The in vivo relevance of these results is further supported by a tissue microarray of breast cancer samples in which we observed correlated expression of Aldehyde dehydrogenase (ALDH) and NIK protein. Our results support the essential involvement of NIK in BCSC phenotypic regulation via ERK1/2 and NF-κB.

摘要

乳腺癌干细胞(BCSCs)过度表达核因子-κB(NF-κB)信号级联反应的组成部分,因此表现出高 NF-κB 活性水平。具有高比例 CSC 的乳腺癌细胞系表现出高 NF-κB 诱导激酶(NIK)表达。NIK 在癌症干细胞调节表型中的作用知之甚少。通过定量 RT-PCR 分析 BCSCs 中的 NIK 表达。通过转染特异性 shRNA 或表达载体来操纵 NIK 水平。通过乳腺球体形成、小鼠异种移植和干细胞标志物表达评估 NIK 在癌症干细胞特性中的作用。BCSCs 表达更高水平的 NIK,通过短发夹(shRNA)抑制 NIK 表达,降低 CSC 标志物的表达,并损害克隆形成能力和肿瘤发生。全基因组表达分析表明,NIK 通过 ERK1/2 途径发挥作用。此外,强制表达 NIK 增加了 BCSC 群体,并增强了乳腺癌细胞的致瘤性。乳腺癌样本的组织微阵列进一步支持了这些结果的体内相关性,我们观察到醛脱氢酶(ALDH)和 NIK 蛋白的表达相关。我们的结果支持 NIK 通过 ERK1/2 和 NF-κB 对 BCSC 表型调节的重要参与。

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