• 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

真核翻译起始因子在膀胱癌中的表达。

Expression of Eukaryotic Translation Initiation Factors in the Urothelial Carcinoma of the Bladder.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Erlangen, Germany.

Dessau Medical Center and Brandenburg Medical School Theodor Fontane, Dessau-Roßlau, Germany.

出版信息

Anticancer Res. 2023 Apr;43(4):1437-1448. doi: 10.21873/anticanres.16292.

DOI:10.21873/anticanres.16292
PMID:36974813
Abstract

BACKGROUND/AIM: Urothelial carcinoma (UC) of the urinary bladder is the second most common tumor in the field of urology and is characterized by a relatively aggressive growth behavior. New therapeutic approaches are required to improve the prognosis of affected patients. We hypothesized a link between dysregulation of eIFs and the development of UC. Therefore, in the present work, we investigated the expression behavior of eIF1, eIF1AY, eIF1AX, eIF2α, eIF3a, eIF3b, eIF4B, eIF4E, eIF4G, eIF5A, eIF5B, and eIF6 in UC compared with that in urothelial tissue.

MATERIALS AND METHODS

Paraffin-embedded tumor tissue samples from 107 patients suffering from UC were examined. Seventy-six patients contained adjacent urothelial tissue. Three tumor tissue cylinders (tumor collective) and two urothelial tissue cylinders (control collective) were collected per patient and embedded in tissue microarray (TMA) blocks. Immunohistochemical staining of the TMA sections was then performed. The staining results were assessed semi-quantitatively. Staining intensities and immunoreactive scores (IRS) of both collectives were compared. In each case, a distinction was made between cytoplasmic and nuclear staining.

RESULTS

Significant up-regulation of eIF1AY, eIF2α, eIF3a, eIF3b, eIF4B, eIF4G, eIF5B, and eIF6 was found in the cytoplasm of UC. In contrast, eIF1 and eIF5A were significantly down-regulated in the cytoplasm of UC. eIF5A and eIF6 were significantly down-regulated in the nuclei of UC.

CONCLUSION

Dysregulation of eIFs in the urothelium of the urinary bladder is linked to carcinogenesis at this site.

摘要

背景/目的:膀胱癌是泌尿外科领域第二大常见肿瘤,其生长行为具有相对侵袭性。需要新的治疗方法来改善受影响患者的预后。我们假设 eIFs 的失调与 UC 的发展之间存在联系。因此,在本研究中,我们研究了 eIF1、eIF1AY、eIF1AX、eIF2α、eIF3a、eIF3b、eIF4B、eIF4E、eIF4G、eIF5A、eIF5B 和 eIF6 在 UC 中的表达行为与尿路上皮组织中的表达行为进行了比较。

材料和方法

对 107 例 UC 患者的石蜡包埋肿瘤组织样本进行了检查。76 例患者包含相邻的尿路上皮组织。每位患者采集 3 个肿瘤组织圆柱体(肿瘤集合)和 2 个尿路上皮组织圆柱体(对照集合),并将其嵌入组织微阵列(TMA)块中。然后对 TMA 切片进行免疫组织化学染色。对染色结果进行半定量评估。比较两个集合的染色强度和免疫反应性评分(IRS)。在每种情况下,均对细胞质和核染色进行区分。

结果

在 UC 的细胞质中发现 eIF1AY、eIF2α、eIF3a、eIF3b、eIF4B、eIF4G、eIF5B 和 eIF6 的表达显著上调。相比之下,UC 细胞质中的 eIF1 和 eIF5A 表达显著下调。UC 细胞核中的 eIF5A 和 eIF6 表达显著下调。

结论

膀胱尿路上皮中 eIFs 的失调与该部位的癌变有关。

相似文献

1
Expression of Eukaryotic Translation Initiation Factors in the Urothelial Carcinoma of the Bladder.真核翻译起始因子在膀胱癌中的表达。
Anticancer Res. 2023 Apr;43(4):1437-1448. doi: 10.21873/anticanres.16292.
2
The Prognostic Significance of Eukaryotic Translation Initiation Factors (eIFs) in Endometrial Cancer.真核翻译起始因子(eIFs)在子宫内膜癌中的预后意义。
Int J Mol Sci. 2019 Dec 6;20(24):6169. doi: 10.3390/ijms20246169.
3
Human Epidermal Growth Factor Receptor 2 Overexpression in Micropapillary and Other Variants of Urothelial Carcinoma.人表皮生长因子受体 2 在微乳头状和其他变异型尿路上皮癌中的过表达。
Eur Urol Focus. 2018 Apr;4(3):399-404. doi: 10.1016/j.euf.2016.06.007. Epub 2016 Jun 21.
4
Utility of the laminin immunohistochemical stain in distinguishing invasive from noninvasive urothelial carcinoma.层粘连蛋白免疫组化染色在鉴别浸润性与非浸润性尿路上皮癌中的应用
J Cancer Res Ther. 2017 Oct-Dec;13(6):947-950. doi: 10.4103/0973-1482.179523.
5
Transient receptor potential vanilloid type 2 (TRPV2) expression in normal urothelium and in urothelial carcinoma of human bladder: correlation with the pathologic stage.瞬时受体电位香草酸亚型2(TRPV2)在人膀胱正常尿路上皮及尿路上皮癌中的表达:与病理分期的相关性
Eur Urol. 2008 Sep;54(3):612-20. doi: 10.1016/j.eururo.2007.10.016. Epub 2007 Oct 16.
6
GATA3 expression in paragangliomas: a pitfall potentially leading to misdiagnosis of urothelial carcinoma.GATA3 在副神经节瘤中的表达:一种潜在导致误诊为尿路上皮癌的陷阱。
Mod Pathol. 2013 Oct;26(10):1365-70. doi: 10.1038/modpathol.2013.76. Epub 2013 Apr 19.
7
Recently described and unusual variants of urothelial carcinoma of the urinary bladder.最近描述的和不常见的膀胱尿路上皮癌变体。
Pathology. 2012 Aug;44(5):407-18. doi: 10.1097/PAT.0b013e3283560172.
8
Invasive micropapillary urothelial carcinoma of the bladder.膀胱浸润性微乳头状尿路上皮癌。
Hum Pathol. 2010 Aug;41(8):1159-64. doi: 10.1016/j.humpath.2009.11.018. Epub 2010 Apr 8.
9
A comprehensive immunohistochemical and molecular approach to the PI3K/AKT/mTOR (phosphoinositide 3-kinase/v-akt murine thymoma viral oncogene/mammalian target of rapamycin) pathway in bladder urothelial carcinoma.全面的免疫组化和分子方法研究膀胱尿路上皮癌中的 PI3K/AKT/mTOR(磷酸肌醇 3-激酶/v-akt 鼠胸腺瘤病毒致癌基因/雷帕霉素的哺乳动物靶标)通路。
BJU Int. 2012 Dec;110(11 Pt C):E1237-48. doi: 10.1111/j.1464-410X.2012.11569.x. Epub 2012 Oct 29.
10
Epigenetic silencing of the dual-role signal mediator, ANGPTL4 in tumor tissues and its overexpression in the urothelial carcinoma microenvironment.肿瘤组织中双重作用信号介质 ANGPTL4 的表观遗传沉默及其在尿路上皮癌微环境中的过表达。
Oncogene. 2018 Feb 1;37(5):673-686. doi: 10.1038/onc.2017.375. Epub 2017 Oct 16.

引用本文的文献

1
ElF5B as a prognostic biomarker and its correlation with infiltrating immune cells in liver cancer.ElF5B作为一种预后生物标志物及其与肝癌中浸润免疫细胞的相关性。
Genes Genomics. 2025 Aug 25. doi: 10.1007/s13258-025-01671-6.
2
Sequestration of ribosomal subunits as inactive 80S by targeting eIF6 limits mitotic exit and cancer progression.通过靶向真核起始因子6(eIF6)将核糖体亚基隔离为无活性的80S核糖体,会限制有丝分裂退出和癌症进展。
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkae1272.
3
G3BP1 and SLU7 Jointly Promote Immune Evasion by Downregulating MHC-I via PI3K/Akt Activation in Bladder Cancer.
G3BP1 和 SLU7 通过激活 PI3K/Akt 下调 MHC-I 共同促进膀胱癌的免疫逃逸。
Adv Sci (Weinh). 2024 Feb;11(7):e2305922. doi: 10.1002/advs.202305922. Epub 2023 Dec 12.