• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

RAGE和SOX2在前列腺良性和恶性病变中的表达比较

Comparative Expression of RAGE and SOX2 in Benign and Malignant Prostatic Lesions.

作者信息

Aboushousha Tarek, Lashen Rana, Abdelnaser Khadega, Helal Noha, Moussa Mona, Omran Zeinab, Eldahshan Samir, El Ganzoury Hossam

机构信息

Department of Pathology, Theodor Bilharz Research Institute, Cairo, Egypt. Email:

出版信息

Asian Pac J Cancer Prev. 2019 Feb 26;20(2):615-620. doi: 10.31557/APJCP.2019.20.2.615.

DOI:10.31557/APJCP.2019.20.2.615
PMID:30806068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6897005/
Abstract

Background: Prostate cancer (PCa) is a common health problem in elderly. RAGE (Receptor for advanced glycation end products) is overexpressed in multiple human cancers. SOX2 (Sex-determining region Y box 2) also functions as an oncoprotein and promotes cancer progression but the mechanisms involved remain largely unknown. Aim: The current study investigated the expression patterns of RAGE and SOX2 in benign and malignant prostate samples in correlation with the histopathological findings in order to evaluate their role as prognostic markers or therapeutic targets. Methods: Immunohistochemical staining for RAGE and SOX2 antibodies was applied on 87 prostatic biopsies [16 of prostatitis, 20 of benign prostatic hyperplasia (BPH) and 51 of PCa]. Results: Expression of RAGE and SOX2 (percentage of positive cells) was significantly higher in PCa lesions compared with prostatitis (p<0.01) and BPH (p<0.0001) and was also significantly higher in prostatitis compared with BPH lesions (p<0.01). Also, percentage of positive RAGE and SOX2 cells showed a significant stepwise increase from Gleason Grade 3 to Grade 5 and were significantly higher in high Gleason Scores (≥8) compared to lower Scores (≤7) with statistical significance (p=0.001). Conclusion: RAGE and SOX2 were up-regulated in prostate cancer lesions, mainly in advanced grades, suggesting an active role of both antigens in the development and progression of prostate cancer and expecting the possibility of their use as therapeutic targets.

摘要

背景

前列腺癌(PCa)是老年人常见的健康问题。晚期糖基化终产物受体(RAGE)在多种人类癌症中过度表达。性别决定区Y框蛋白2(SOX2)也作为一种癌蛋白发挥作用并促进癌症进展,但其涉及的机制在很大程度上仍不清楚。目的:本研究调查RAGE和SOX2在良性和恶性前列腺样本中的表达模式,并与组织病理学结果相关联,以评估它们作为预后标志物或治疗靶点的作用。方法:对87例前列腺活检组织[16例前列腺炎、20例良性前列腺增生(BPH)和51例PCa]进行RAGE和SOX2抗体的免疫组织化学染色。结果:与前列腺炎(p<0.01)和BPH(p<0.0001)相比,PCa病变中RAGE和SOX2的表达(阳性细胞百分比)显著更高,与BPH病变相比,前列腺炎中的表达也显著更高(p<0.01)。此外,RAGE和SOX2阳性细胞百分比从Gleason分级3级到5级呈显著逐步增加,与较低评分(≤7)相比,高Gleason评分(≥8)中的表达显著更高,具有统计学意义(p=0.001)。结论:RAGE和SOX2在前列腺癌病变中上调,主要在高级别中,表明这两种抗原在前列腺癌的发生和进展中发挥积极作用,并有望将其用作治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/6897005/9d84f6d71e68/APJCP-20-615-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/6897005/730a0e0654dd/APJCP-20-615-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/6897005/9d84f6d71e68/APJCP-20-615-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/6897005/730a0e0654dd/APJCP-20-615-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/6897005/9d84f6d71e68/APJCP-20-615-g002.jpg

相似文献

1
Comparative Expression of RAGE and SOX2 in Benign and Malignant Prostatic Lesions.RAGE和SOX2在前列腺良性和恶性病变中的表达比较
Asian Pac J Cancer Prev. 2019 Feb 26;20(2):615-620. doi: 10.31557/APJCP.2019.20.2.615.
2
Prostate health index and prostate cancer gene 3 score but not percent-free Prostate Specific Antigen have a predictive role in differentiating histological prostatitis from PCa and other nonneoplastic lesions (BPH and HG-PIN) at repeat biopsy.前列腺健康指数和前列腺癌基因3评分,而非游离前列腺特异性抗原百分比,在重复活检时对鉴别组织学前列腺炎与前列腺癌及其他非肿瘤性病变(良性前列腺增生和高级别前列腺上皮内瘤变)具有预测作用。
Urol Oncol. 2015 Oct;33(10):424.e17-23. doi: 10.1016/j.urolonc.2015.05.032. Epub 2015 Jul 7.
3
Diagnostic and prognostic value of serum miR-15a and miR-16-1 expression among egyptian patients with prostate cancer.血清 miR-15a 和 miR-16-1 表达在埃及前列腺癌患者中的诊断和预后价值。
IUBMB Life. 2018 May;70(5):437-444. doi: 10.1002/iub.1733. Epub 2018 Mar 9.
4
Immunohistochemical expression of topoisomerase II alpha and Her-2/neu in prostatic carcinoma and benign prostatic hyperplasia.拓扑异构酶IIα和Her-2/neu在前列腺癌和良性前列腺增生中的免疫组化表达
J Egypt Natl Canc Inst. 2008 Jun;20(2):158-67.
5
Immunohistochemical expression of interleukin-2 receptor and interleukin-6 in patients with prostate cancer and benign prostatic hyperplasia: association with asymptomatic inflammatory prostatitis NIH category IV.白细胞介素-2受体和白细胞介素-6在前列腺癌和良性前列腺增生患者中的免疫组化表达:与无症状性炎症性前列腺炎NIH IV类的关联
Scand J Urol. 2015 Apr;49(2):120-6. doi: 10.3109/21681805.2014.971427. Epub 2014 Nov 3.
6
Differential expression of Low density lipoprotein Receptor-related Protein 1 (LRP-1) and matrix metalloproteinase-9 (MMP-9) in prostate gland: From normal to malignant lesions.低密度脂蛋白受体相关蛋白1(LRP-1)和基质金属蛋白酶-9(MMP-9)在前列腺中的差异表达:从正常病变到恶性病变
Pathol Res Pract. 2017 Jan;213(1):66-71. doi: 10.1016/j.prp.2016.11.008. Epub 2016 Nov 24.
7
Klf4 transcription factor is expressed in the cytoplasm of prostate cancer cells.Klf4 转录因子在前列腺癌细胞的细胞质中表达。
Eur J Cancer. 2013 Mar;49(4):955-63. doi: 10.1016/j.ejca.2012.09.023. Epub 2012 Oct 22.
8
Oxidative stress parameters in patients with prostate cancer, benign prostatic hyperplasia and asymptomatic inflammatory prostatitis: A prospective controlled study.前列腺癌、良性前列腺增生和无症状性炎性前列腺炎患者的氧化应激参数:一项前瞻性对照研究。
Adv Clin Exp Med. 2017 Oct;26(7):1095-1099. doi: 10.17219/acem/66837.
9
Can expressed prostatic secretions effect prostate biopsy decision of urologist?前列腺液的表达是否会影响泌尿科医生对前列腺活检的决策?
Int Braz J Urol. 2019 Mar-Apr;45(2):246-252. doi: 10.1590/S1677-5538.IBJU.2018.0292.
10
The diagnostic utility of novel immunohistochemical marker ERG in the workup of prostate biopsies with "atypical glands suspicious for cancer".新型免疫组织化学标志物 ERG 在“疑似癌的非典型腺体”前列腺活检中的诊断效用。
Am J Surg Pathol. 2011 Apr;35(4):608-14. doi: 10.1097/PAS.0b013e31820bcd2d.

引用本文的文献

1
The role of SOX transcription factors in prostate cancer: Focusing on SOX2.SOX转录因子在前列腺癌中的作用:聚焦于SOX2
Genes Dis. 2025 May 21;12(6):101692. doi: 10.1016/j.gendis.2025.101692. eCollection 2025 Nov.
2
The molecular pathogenesis of SOX2 in prostate cancer.SOX2在前列腺癌中的分子发病机制。
Discov Oncol. 2025 Feb 20;16(1):215. doi: 10.1007/s12672-025-01972-y.
3
RAGE as a Novel Biomarker for Prostate Cancer: A Systematic Review and Meta-Analysis.RAGE作为前列腺癌的一种新型生物标志物:系统评价与Meta分析

本文引用的文献

1
Immunohistochemical and Biochemical Expression Patterns of TTF-1, RAGE, GLUT-1 and SOX2 in HCV-Associated Hepatocellular Carcinomas.TTF-1、RAGE、GLUT-1和SOX2在丙型肝炎病毒相关肝细胞癌中的免疫组化及生化表达模式
Asian Pac J Cancer Prev. 2018 Jan 27;19(1):219-227. doi: 10.22034/APJCP.2018.19.1.219.
2
High ASMA Fibroblasts and Low Cytoplasmic HMGB1 Breast Cancer Cells Predict Poor Prognosis.高 ASMA 成纤维细胞和低细胞质 HMGB1 的乳腺癌细胞预示着不良预后。
Clin Breast Cancer. 2017 Oct;17(6):441-452.e2. doi: 10.1016/j.clbc.2017.04.007. Epub 2017 Apr 21.
3
Increased Expression of the Receptor for Advanced Glycation End-Products (RAGE) Is Associated with Advanced Breast Cancer Stage.
Cancers (Basel). 2023 Oct 9;15(19):4889. doi: 10.3390/cancers15194889.
4
Role of HMGB1 in Cisplatin-Persistent Lung Adenocarcinoma Cell Lines.HMGB1在顺铂耐药肺腺癌细胞系中的作用
Front Oncol. 2021 Dec 13;11:750677. doi: 10.3389/fonc.2021.750677. eCollection 2021.
5
The impact of receptor of advanced glycation end-products polymorphisms on prostate cancer progression and clinicopathological characteristics.晚期糖基化终产物受体多态性对前列腺癌进展及临床病理特征的影响。
J Cell Mol Med. 2021 Nov;25(22):10761-10769. doi: 10.1111/jcmm.17025. Epub 2021 Oct 27.
晚期乳腺癌患者中晚期糖基化终产物受体(RAGE)的表达增加。
Oncol Res Treat. 2016;39(10):622-628. doi: 10.1159/000449326. Epub 2016 Sep 15.
4
Hypoxia regulates SOX2 expression to promote prostate cancer cell invasion and sphere formation.缺氧调节SOX2表达以促进前列腺癌细胞侵袭和球状体形成。
Am J Cancer Res. 2016 May 1;6(5):1078-88. eCollection 2016.
5
SOX2 boosts major tumor progression genes in prostate cancer and is a functional biomarker of lymph node metastasis.SOX2促进前列腺癌主要肿瘤进展基因,并且是淋巴结转移的功能性生物标志物。
Oncotarget. 2016 Mar 15;7(11):12372-85. doi: 10.18632/oncotarget.6029.
6
Cancer incidence in egypt: results of the national population-based cancer registry program.埃及的癌症发病率:基于全国人口的癌症登记项目结果
J Cancer Epidemiol. 2014;2014:437971. doi: 10.1155/2014/437971. Epub 2014 Sep 21.
7
SOX2 and cancer: current research and its implications in the clinic.SOX2 与癌症:当前的研究及其在临床中的意义。
Clin Transl Med. 2014 Jul 4;3:19. doi: 10.1186/2001-1326-3-19. eCollection 2014.
8
Increased SOX2 expression in less differentiated breast carcinomas and their lymph node metastases.在分化程度较低的乳腺癌及其淋巴结转移中,SOX2 的表达增加。
Histopathology. 2014 Mar;64(4):494-503. doi: 10.1111/his.12257. Epub 2013 Nov 28.
9
Elevated expression of SOX2 and FGFR1 in correlation with poor prognosis in patients with small cell lung cancer.SOX2和FGFR1的高表达与小细胞肺癌患者的不良预后相关。
Int J Clin Exp Pathol. 2013 Nov 15;6(12):2846-54. eCollection 2013.
10
Predicting the risk of bone metastasis in prostate cancer.预测前列腺癌骨转移的风险。
Cancer Treat Rev. 2014 Feb;40(1):3-11. doi: 10.1016/j.ctrv.2013.07.001. Epub 2013 Jul 26.