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前列腺癌中的Stat3激活

Stat3 activation in prostatic carcinomas.

作者信息

Dhir Rajiv, Ni Zuyao, Lou Wei, DeMiguel Fernando, Grandis Jennifer Rubin, Gao Allen C

机构信息

Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

出版信息

Prostate. 2002 Jun 1;51(4):241-6. doi: 10.1002/pros.10079.

Abstract

BACKGROUND

Activated Stat3 is found in various types of immortal cell lines and cancers. We and others have previously demonstrated that Stat3 is constitutively activated in rat and human prostate cancer cell lines, and that Stat3 activation is involved in IL-6-mediated signaling transduction in prostate cancer cells. The aim of this study is to examine quantitative Stat3 activity in benign and malignant human prostate tissues and analyze the association between Stat3 activity levels and the clinical and pathologic parameters.

METHODS

Stat3 activity levels were analyzed in a total of 104 human primary prostate tissues using electromobility shift assay and immunohistochemical staining for phosphorylated Stat3. The tissue samples used were 42 prostate carcinomas, 42 matched normal prostate tissues from patients with prostatic adenocarcinoma (normal adjacent to tumor), and 20 normal prostate tissues from organ donors.

RESULTS

Significantly higher levels of constitutive Stat3 activity were detected in both prostate carcinomas and the matched normal prostate tissues adjacent to tumors compared to the normal prostates from donors without prostate cancer. There was no significant difference of Stat3 activity in foci of tumor and normal prostate tissue adjacent to tumor. No correlation was seen between Stat3 activity and Gleason grade or serum PSA levels in samples from prostate carcinomas.

CONCLUSIONS

These results indicate that Stat3 is constitutively activated in prostate cancer. The high level of Stat3 activity in both the prostate carcinomas and the normal prostate tissues adjacent to tumors suggests that Stat3 activation may occur before detectable histological alterations of the prostate.

摘要

背景

活化的Stat3存在于多种类型的永生化细胞系和癌症中。我们及其他研究人员先前已证明,Stat3在大鼠和人类前列腺癌细胞系中持续活化,且Stat3活化参与前列腺癌细胞中白细胞介素-6介导的信号转导。本研究旨在检测人良性和恶性前列腺组织中Stat3的定量活性,并分析Stat3活性水平与临床及病理参数之间的关联。

方法

使用电泳迁移率变动分析和磷酸化Stat3免疫组织化学染色,对总共104个人原发性前列腺组织的Stat3活性水平进行分析。所用组织样本包括42例前列腺癌、42例来自前列腺腺癌患者的配对正常前列腺组织(肿瘤旁正常组织)以及20例来自器官供体的正常前列腺组织。

结果

与无前列腺癌的供体正常前列腺相比,前列腺癌及肿瘤旁配对正常前列腺组织中均检测到显著更高水平的持续性Stat3活性。肿瘤灶与肿瘤旁正常前列腺组织中的Stat3活性无显著差异。前列腺癌样本中Stat3活性与Gleason分级或血清前列腺特异抗原(PSA)水平之间无相关性。

结论

这些结果表明Stat3在前列腺癌中持续活化。前列腺癌及肿瘤旁正常前列腺组织中Stat3活性的高水平表明,Stat3活化可能在前列腺可检测到的组织学改变之前就已发生。

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