• 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

miR-628-5p 是膀胱癌潜在的新型预后生物标志物,与免疫浸润相关。

miR-628-5p is a Potential Novel Prognosis Biomarker, Associated with Immune Infiltration in Bladder Urothelial Carcinoma.

机构信息

Department of Urology, Shantou Central Hospital, Jinping District, Shantou 515031, China.

出版信息

Curr Pharm Des. 2023;29(31):2477-2488. doi: 10.2174/0113816128254621231017062923.

DOI:10.2174/0113816128254621231017062923
PMID:37916623
Abstract

BACKGROUND

microRNA-628-5p (miR-628-5p) has a significant impact on certain types of cancer. The precise function of miR-628-5p in the context of bladder urothelial carcinoma (BLCA) remains ambiguous.

OBJECTIVE

We aimed to investigate the role of miR-628-5p in BLCA.

METHODS

The samples were collected from The Cancer Genome Atlas (TCGA). Statistics were employed to evaluate the correlation and predictive significance of miR-628-5p. We analyzed the target genes and regulatory network of miR-628-5p and the correlation between miR-628-5p and immune infiltration. The expression of miR-628-5p in BLCA cells was confirmed by quantitative reverse-transcription PCR (qRT-PCR).

RESULTS

miR-628-5p exhibited differential expression across various types of cancer. There was a significant association between high expression of miR-628-5p and primary therapy outcome (p < 0.05). High expression of miR-628-5p was observed to be associated with poorer overall survival (HR: 1.42; 95% CI: 1.06-1.90; p = 0.02), progress free survival (HR: 1.57; 95% CI: 1.17-2.11; p = 0.003), and disease specific survival (HR: 1.83; 95% CI: 1.28-2.62; p = 0.001) in BLCA. miR-628-5p was an independent prognostic factor in BLCA and may be involved in the development of the disease through various pathways, including focal adhesion, ECM-receptor interaction, PI3K-Akt signaling pathway, and MAPK signaling pathway, and among others. miR-628-5p expression was significantly correlated with immune infiltration in BLCA patients. Compared to normal bladder epithelial cells, BLCA cell lines exhibited a significant upregulation of miR-628-5p.

CONCLUSION

It is possible that miR-628-5p could serve as a hopeful therapeutic target and prognostic biomarker for individuals with BLCA.

摘要

背景

microRNA-628-5p(miR-628-5p)对某些类型的癌症有显著影响。miR-628-5p 在膀胱尿路上皮癌(BLCA)中的精确作用仍不清楚。

目的

我们旨在研究 miR-628-5p 在 BLCA 中的作用。

方法

本研究样本取自癌症基因组图谱(TCGA)。采用统计学方法评估 miR-628-5p 的相关性和预测意义。我们分析了 miR-628-5p 的靶基因和调控网络,以及 miR-628-5p 与免疫浸润的相关性。通过定量逆转录 PCR(qRT-PCR)验证 BLCA 细胞中 miR-628-5p 的表达。

结果

miR-628-5p 在各种癌症中表现出差异表达。miR-628-5p 的高表达与原发治疗结局显著相关(p<0.05)。miR-628-5p 高表达与总生存期(HR:1.42;95%CI:1.06-1.90;p=0.02)、无进展生存期(HR:1.57;95%CI:1.17-2.11;p=0.003)和疾病特异性生存期(HR:1.83;95%CI:1.28-2.62;p=0.001)较差相关。miR-628-5p 是 BLCA 的独立预后因素,可能通过多种途径参与疾病的发生发展,包括局灶黏附、ECM-受体相互作用、PI3K-Akt 信号通路和 MAPK 信号通路等。miR-628-5p 的表达与 BLCA 患者的免疫浸润显著相关。与正常膀胱上皮细胞相比,BLCA 细胞系中 miR-628-5p 的表达显著上调。

结论

miR-628-5p 可能成为 BLCA 患者有希望的治疗靶点和预后生物标志物。

相似文献

1
miR-628-5p is a Potential Novel Prognosis Biomarker, Associated with Immune Infiltration in Bladder Urothelial Carcinoma.miR-628-5p 是膀胱癌潜在的新型预后生物标志物,与免疫浸润相关。
Curr Pharm Des. 2023;29(31):2477-2488. doi: 10.2174/0113816128254621231017062923.
2
Prognostic value of COL10A1 and its correlation with tumor-infiltrating immune cells in urothelial bladder cancer: A comprehensive study based on bioinformatics and clinical analysis validation.COL10A1 在尿路上皮膀胱癌中的预后价值及其与肿瘤浸润免疫细胞的相关性:基于生物信息学和临床分析验证的综合研究。
Front Immunol. 2023 Mar 17;14:955949. doi: 10.3389/fimmu.2023.955949. eCollection 2023.
3
Prognostic significance and immunoinfiltration analysis of genes associated with epithelial-mesenchymal transition and energy metabolism in bladder urothelial carcinoma.与膀胱尿路上皮癌上皮-间质转化和能量代谢相关基因的预后意义及免疫浸润分析。
Aging (Albany NY). 2023 Nov 24;15(22):13312-13328. doi: 10.18632/aging.205242.
4
TEAD4 functions as a prognostic biomarker and triggers EMT via PI3K/AKT pathway in bladder cancer.TEAD4 在膀胱癌中作为预后生物标志物,通过 PI3K/AKT 通路触发 EMT。
J Exp Clin Cancer Res. 2022 May 17;41(1):175. doi: 10.1186/s13046-022-02377-3.
5
PRR11 is a prognostic biomarker and correlates with immune infiltrates in bladder urothelial carcinoma.PRR11 是一种预后生物标志物,与膀胱尿路上皮癌的免疫浸润相关。
Sci Rep. 2023 Feb 4;13(1):2051. doi: 10.1038/s41598-023-29316-2.
6
Uncovering the potential functions of lymph node metastasis-associated aberrant methylation differentially expressed genes and their association with the immune infiltration and prognosis in bladder urothelial carcinoma.揭示淋巴结转移相关异常甲基化差异表达基因的潜在功能及其与膀胱癌免疫浸润和预后的关系。
PeerJ. 2023 Apr 24;11:e15284. doi: 10.7717/peerj.15284. eCollection 2023.
7
PVT1 is a prognostic marker associated with immune invasion of bladder urothelial carcinoma.PVT1 是与膀胱尿路上皮癌免疫浸润相关的预后标志物。
Math Biosci Eng. 2022 Jan;19(1):169-190. doi: 10.3934/mbe.2022009. Epub 2021 Nov 9.
8
TUBA1C is a potential new prognostic biomarker and promotes bladder urothelial carcinoma progression by regulating the cell cycle.TUBA1C 是一种潜在的新的预后生物标志物,通过调节细胞周期促进膀胱尿路上皮癌的进展。
BMC Cancer. 2023 Aug 1;23(1):716. doi: 10.1186/s12885-023-11209-2.
9
Transcriptional expressions of hsa-mir-183 predicted target genes as independent indicators for prognosis in bladder urothelial carcinoma.hsa-mir-183 预测靶基因的转录表达作为膀胱癌的独立预后指标。
Aging (Albany NY). 2022 May 3;14(9):3782-3800. doi: 10.18632/aging.204040.
10
Comprehensive analysis of PRPF19 immune infiltrates, DNA methylation, senescence-associated secretory phenotype and ceRNA network in bladder cancer.膀胱癌中 PRPF19 免疫浸润物、DNA 甲基化、衰老相关分泌表型和 ceRNA 网络的综合分析。
Front Immunol. 2023 Nov 6;14:1289198. doi: 10.3389/fimmu.2023.1289198. eCollection 2023.

引用本文的文献

1
ZP3 Expression in Pancreatic Adenocarcinoma: Its Implications for the Prognosis and Therapy.胰腺癌中ZP3的表达:其对预后和治疗的意义
Protein Pept Lett. 2025;32(2):124-138. doi: 10.2174/0109298665350171241204153202.