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PTEN Tumor Suppressor Network in PI3K-Akt Pathway Control.PI3K-Akt信号通路调控中的PTEN肿瘤抑制网络
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HSP90 inhibition is effective in breast cancer: a phase II trial of tanespimycin (17-AAG) plus trastuzumab in patients with HER2-positive metastatic breast cancer progressing on trastuzumab.HSP90 抑制在乳腺癌中有效:替吡法尼(17-AAG)联合曲妥珠单抗治疗曲妥珠单抗进展的 HER2 阳性转移性乳腺癌的 II 期试验。
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4
Expression status and prognostic significance of mammalian target of rapamycin pathway members in urothelial carcinoma of urinary bladder after cystectomy.膀胱切除术后膀胱癌中哺乳动物雷帕霉素靶蛋白通路成员的表达状态与预后意义。
Cancer. 2010 Dec 1;116(23):5517-26. doi: 10.1002/cncr.25502. Epub 2010 Oct 11.
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17-Allylamino-17-demethoxygeldanamycin induces downregulation of critical Hsp90 protein clients and results in cell cycle arrest and apoptosis of human urinary bladder cancer cells.17-烯丙氨基-17-去甲氧格尔德霉素诱导关键 HSP90 蛋白客户下调,导致人膀胱癌细胞周期停滞和凋亡。
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DJ-1: a novel independent prognostic marker for survival in glottic squamous cell carcinoma.DJ-1:声门型鳞状细胞癌生存的新型独立预后标志物。
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10
Activation of the PI3K/AKT pathway induces urothelial carcinoma of the renal pelvis: identification in human tumors and confirmation in animal models.PI3K/AKT信号通路的激活可诱发肾盂尿路上皮癌:在人类肿瘤中的鉴定及在动物模型中的证实。
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DJ-1和HSP90α的过表达以及PTEN的缺失与膀胱浸润性尿路上皮癌相关:可能的预后标志物。

Overexpression of DJ-1 and HSP90α, and loss of PTEN associated with invasive urothelial carcinoma of urinary bladder: Possible prognostic markers.

作者信息

Lee Hojung, Choi Seung Kyu, Ro Jae Y

机构信息

Department of Pathology, Eulji Medical Center, Eulji University School of Medicine, Seoul, Republic of Korea.

出版信息

Oncol Lett. 2012 Mar;3(3):507-512. doi: 10.3892/ol.2011.522. Epub 2011 Dec 13.

DOI:10.3892/ol.2011.522
PMID:22740940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3362422/
Abstract

DJ-1 and HSP90α play a significant role in the progression of various types of cancer and are known to be associated with phosphatase and tensin homolog deleted on chromosome 10 (PTEN), PI3K-p110α and pAkt, the signaling molecule proteins from the phosphatidylinositol 3-kinase (PI3K) pathway. However, the expression of these proteins and their clinical significance are not well characterized in urothelial carcinoma (UC). Immunohistochemical analysis of DJ-1, HSP90α, PTEN, pAkt and PI3K-p110α expression was performed on tumor samples from 102 patients with UC to assess the relationship between the expression of each protein and the pathological parameters. The expression of DJ-1 and HSP90α was positively correlated with the pathological stage of UC, whereas PTEN expression negatively correlated with, not only the pathological stage, but also the growth pattern and histological grade of UC. Although PI3K-p110α expression was significantly correlated with DJ-1 as well as PTEN expression in UC, PI3K-p110α expression itself failed to reveal any significant correlation with the clinicopathological parameters. In conclusion, the overexpression of DJ-1 and HSP90α, and a loss of PTEN are associated with invasive UC, and PI3K-p110α expression is correlated with DJ-1 and PTEN expression in UC.

摘要

DJ-1和HSP90α在多种癌症进展中发挥重要作用,且已知与10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)、PI3K-p110α及pAkt相关,这些是来自磷脂酰肌醇3激酶(PI3K)信号通路的分子蛋白。然而,这些蛋白在尿路上皮癌(UC)中的表达及其临床意义尚未得到充分表征。对102例UC患者的肿瘤样本进行了DJ-1、HSP90α、PTEN、pAkt和PI3K-p110α表达的免疫组化分析,以评估每种蛋白表达与病理参数之间的关系。DJ-1和HSP90α的表达与UC的病理分期呈正相关,而PTEN表达不仅与病理分期呈负相关,还与UC的生长模式和组织学分级呈负相关。虽然PI3K-p110α表达在UC中与DJ-1以及PTEN表达显著相关,但PI3K-p110α表达本身与临床病理参数未显示出任何显著相关性。总之,DJ-1和HSP90α的过表达以及PTEN的缺失与浸润性UC相关,且PI3K-p110α表达在UC中与DJ-1和PTEN表达相关。