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p53凋亡刺激蛋白的抑制性成员在膀胱癌中过度表达并与其进展相关。

Inhibitory member of the apoptosis-stimulating protein of p53 is overexpressed in bladder cancer and correlated to its progression.

作者信息

Wu Ziyu, Wang Sugui, Xue Peng, Wang Shoulin, Wang Gongcheng, Zhang Wei

机构信息

Department of Urology, the First Affiliated Hospital of Nanjing Medical University Department of Urology, Affiliated Huai'an Hospital of Xuzhou Medical University Department of Urology, the First People's Hospital of Lianyungang School of Public Health, Nanjing Medical University Department of Urology, Huai'an First People's Hospital, Nanjing Medical University, Jiangsu, China.

出版信息

Medicine (Baltimore). 2017 May;96(19):e6640. doi: 10.1097/MD.0000000000006640.

Abstract

Several lines of direct evidence show that inhibitory member of the apoptosis-stimulating protein of p53 (iASPP) has an important function in cancer progression. However, its expression pattern and relationship with clinical pathologic characteristics in bladder cancer (BC) have not been completely elucidated. In this study, firstly, samples from 3 patients with invasive BC were detected by liquid chromatography tandem mass spectrometry to confirm overexpression of iASPP in BC, then samples from patients with noninvasive and invasive BC were detected by real-time polymerase chain reaction, Western blot, and tissue microarry immunohistochemistry. The relationship between iASPP expression and various clinicopathological features was investigated. The results showed m-RNA and protein of iASPP were overexpressed in BC and the rate of iASPP-positive cells was positively correlated with Union for International Cancer Control-Tumor, Node, Metastases stage, histologic grade, lymph node metastasis and poor overall survive. The data demonstrate that iASPP is overexpressed in BC and promotes the malignancy of BC. iASPP maybe serve as a potential therapeutic target for BC.

摘要

多条直接证据表明,p53凋亡刺激蛋白的抑制成员(iASPP)在癌症进展中具有重要作用。然而,其在膀胱癌(BC)中的表达模式及其与临床病理特征的关系尚未完全阐明。在本研究中,首先,通过液相色谱串联质谱法检测了3例浸润性BC患者的样本,以证实iASPP在BC中的过表达,然后通过实时聚合酶链反应、蛋白质免疫印迹法和组织芯片免疫组化检测了非浸润性和浸润性BC患者的样本。研究了iASPP表达与各种临床病理特征之间的关系。结果显示,iASPP的mRNA和蛋白在BC中过表达,iASPP阳性细胞率与国际癌症控制联盟-肿瘤、淋巴结、转移分期、组织学分级、淋巴结转移及总体生存率差呈正相关。数据表明,iASPP在BC中过表达并促进BC的恶性程度。iASPP可能作为BC的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc52/5428572/8c9ec5eb54eb/medi-96-e6640-g002.jpg

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