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Rhomboid domain-containing protein 1 promotes breast cancer progression by regulating the p-Akt and CDK2 levels

机译:含菱形结构域的蛋白1通过调节p-Akt和CDK2的水平促进乳腺癌的进展

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Our previous work revealed that rhomboid domain-containing protein 1 (RHBDD1) participates in the modulation of cell growth and apoptosis in colorectal cancer cells. This study aimed to investigate the function of RHBDD1 in regulating breast cancer progression and its underlying molecular basis. Immunohistochemistry was performed to evaluate RHBDD1 expression in 116 breast cancer tissue and 39 adjacent normal tissue and expression of RHBDD1, phospho-Akt (p-Akt) and cyclin-dependent kinase 2 (CDK2) in the same 84 breast cancer specimens. RHBDD1-knock-out cells were established using breast cancer cell lines. In vitro studies were carried out to estimate the function of RHBDD1 in cell proliferation, migration and invasion. Fluorescence microscopy assay and flow cytometric analysis were used to measure apoptosis and cell cycle regulation. RNA sequencing and western blot analysis were used to investigate the molecular mechanisms of RHBDD1. RHBDD1 was highly up-regulated in breast cancer tissue compared with that in normal tissue and associated with pathological tumor (pT) stage, pathological tumor-node-metastasis (pTNM) stage and estrogen receptor (ER) expression. RHBDD1 up-regulation was associated with poor prognosis in several subtypes of breast cancer. Deletion of RHBDD1 promoted apoptosis and suppressed proliferation, migration and invasion in breast cancer cells. RHBDD1 deletion suppressed Akt activation and decreased CDK2 protein level via proteasome pathway, thus inhibited cell cycle progression and G1/S phase transition. Moreover, the protein level of RHBDD1, p-Akt and CDK2 was significantly positively correlated in breast cancer tissue. Our study reveals that RHBDD1 promotes breast cancer progression by regulating p-Akt and CDK2 protein levels, and might be a potential biomarker and prognostic indicator for breast cancer patients.
机译:我们以前的工作表明,含有菱形结构域的蛋白1(RHBDD1)参与了大肠癌细胞中细胞生长和凋亡的调节。这项研究旨在调查RHBDD1在调节乳腺癌进展中的功能及其潜在的分子基础。进行免疫组织化学以评估在相同的84个乳腺癌标本中RHBDD1在116个乳腺癌组织和39个邻近正常组织中的表达以及RHBDD1,phospho-Akt(p-Akt)和细胞周期蛋白依赖性激酶2(CDK2)的表达。使用乳腺癌细胞系建立了RHBDD1敲除细胞。进行了体外研究以评估RHBDD1在细胞增殖,迁移和侵袭中的功能。荧光显微镜法和流式细胞仪分析用于测量细胞凋亡和细胞周期调节。 RNA测序和蛋白质印迹分析被用来研究RHBDD1的分子机制。与正常组织相比,乳腺癌组织中的RHBDD1高度上调,并且与病理性肿瘤(pT)分期,病理性肿瘤淋巴结转移(pTNM)分期和雌激素受体(ER)表达有关。在几种亚型的乳腺癌中,RHBDD1上调与预后不良有关。 RHBDD1的缺失促进了乳腺癌细胞的凋亡并抑制了其增殖,迁移和侵袭。 RHBDD1缺失通过蛋白酶体途径抑制Akt激活并降低CDK2蛋白水平,从而抑制细胞周期进程和G1 / S相变。此外,在乳腺癌组织中,RHBDD1,p-Akt和CDK2的蛋白质水平显着正相关。我们的研究表明,RHBDD1通过调节p-Akt和CDK2蛋白水平促进乳腺癌的进展,并且可能是乳腺癌患者的潜在生物标志物和预后指标。

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