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首页> 外文期刊>Molecular medicine. >Correlation between PDZK1, Cdc37, Akt and Breast Cancer Malignancy: The Role of PDZK1 in Cell Growth through Akt Stabilization by Increasing and Interacting with Cdc37
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Correlation between PDZK1, Cdc37, Akt and Breast Cancer Malignancy: The Role of PDZK1 in Cell Growth through Akt Stabilization by Increasing and Interacting with Cdc37

机译:PDZK1,Cdc37,Akt和乳腺癌恶性肿瘤之间的相关性:PDZK1通过增加和与Cdc37的相互作用通过Akt稳定化在细胞生长中的作用

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PDZ domain containing 1 (PDZK1) is a scaffold protein that plays a role in the fate of several proteins. Estrogen can induce PDZK1gene expression; however, our recent report showed that PDZK1 expression in the breast cancer cell line MCF-7 is indirect and involvesinsulin-like growth factor (IGF)-1 receptor function. Such a relationship was established in cell culture systems and humanbreast cancer tissues. Here we show that overexpression of PDZK1 promoted an increase in cyclin D1 and enhanced anchorageindependentgrowth of MCF-7 cells in the absence of 17β-estradiol, suggesting that PDZK1 harbors oncogenic activity. Indeed,PDKZ1 overexpression enhanced epidermal growth factor receptor (EGFR)-stimulated MEK/ERK1/2 signaling and IGF-induced Aktphosphorylation. PDZK1 appeared to play this role, in part, by stabilizing the integrity of the growth promoting factors Akt, humanepidermal growth factor receptor 2 (Her2/Neu) and EGFR. Increased Akt levels occurred via a decrease in the ubiquitination ofthe kinase. PDZK1 overexpression was associated with resistance to paclitaxel/5-fluorouracil/etoposide only at low concentrations.Although the increased stability of Akt was sensitive to heat shock protein 90 (HSP90) inhibition, increased levels of the cochaperonecell division cycle 37 (Cdc37), as well as its ability to bind PDZK1, appear to play a larger role in kinase stability. Using humantissue microarrays, we show strong positive correlation between PDZK1, Akt and Cdc37 protein levels, and all correlated withhuman breast malignancy. There were no positive correlations between PDZK1 and Cdc37 at the mRNA levels, confirming our invitro studies. These results demonstrate a relationship between PDZK1, Akt and Cdc37, and potentially Her2/Neu and EGFR, inbreast cancer, representing a new axis that can be targeted therapeutically to reduce the burden of human breast cancer.
机译:包含1的PDZ域(PDZK1)是一种支架蛋白,在几种蛋白的命运中起作用。雌激素可诱导PDZK1基因表达;但是,我们最近的报告显示PDZK1在乳腺癌细胞MCF-7中的表达是间接的,并且涉及胰岛素样生长因子(IGF)-1受体功能。在细胞培养系统和人类乳腺癌组织中建立了这样的关系。在这里,我们显示PDZK1的过表达在没有17β-雌二醇的情况下促进细胞周期蛋白D1的增加和MCF-7细胞锚定非依赖性生长的增加,表明PDZK1具有致癌活性。确实,PDKZ1过表达增强了表皮生长因子受体(EGFR)刺激的MEK / ERK1 / 2信号转导和IGF诱导的Akt磷酸化。 PDZK1似乎部分通过稳定生长促进因子Akt,人表皮生长因子受体2(Her2 / Neu)和EGFR的完整性发挥了作用。通过减少激酶的泛素化,增加了Akt水平。 PDZK1的过表达仅在低浓度下与对紫杉醇/ 5-氟尿嘧啶/依托泊苷的耐药有关。尽管Akt的稳定性增加对热休克蛋白90(HSP90)抑制敏感,但伴随的伴侣细胞分裂周期37(Cdc37)的水平升高以及其结合PDZK1的能力,似乎在激酶稳定性中起着更大的作用。使用人组织微阵列,我们显示PDZK1,Akt和Cdc37蛋白水平之间有很强的正相关性,所有这些都与人乳腺恶性肿瘤相关。在mRNA水平上PDZK1和Cdc37之间没有正相关,证实了我们的体外研究。这些结果表明PDZK1,Akt和Cdc37与潜在的Her2 / Neu和EGFR乳腺癌之间的关系,代表了可以治疗性降低人类乳腺癌负担的新轴。

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