• 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

TP53、CDKN2A、SMAD4和KRAS在胰腺癌中的意义

Significance of TP53, CDKN2A, SMAD4 and KRAS in Pancreatic Cancer.

作者信息

Stefanoudakis Dimitrios, Frountzas Maximos, Schizas Dimitrios, Michalopoulos Nikolaos V, Drakaki Alexandra, Toutouzas Konstantinos G

机构信息

First Propaedeutic Department of Surgery, Hippocration General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.

First Department of Surgery, Laikon General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.

出版信息

Curr Issues Mol Biol. 2024 Mar 23;46(4):2827-2844. doi: 10.3390/cimb46040177.

DOI:10.3390/cimb46040177
PMID:38666907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11049225/
Abstract

The present review demonstrates the major tumor suppressor genes, including TP53, CDKN2A and SMAD4, associated with pancreatic cancer. Each gene's role, prevalence and impact on tumor development and progression are analyzed, focusing on the intricate molecular landscape of pancreatic cancer. In addition, this review underscores the prognostic significance of specific mutations, such as loss of TP53, and explores some potential targeted therapies tailored to these molecular signatures. The findings highlight the importance of genomic analyses for risk assessment, early detection and the design of personalized treatment approaches in pancreatic cancer. Overall, this review provides a comprehensive analysis of the molecular intricacies of pancreatic tumors, paving the way for more effective and tailored therapeutic interventions.

摘要

本综述展示了与胰腺癌相关的主要肿瘤抑制基因,包括TP53、CDKN2A和SMAD4。分析了每个基因在肿瘤发生和进展中的作用、发生率及影响,重点关注胰腺癌复杂的分子格局。此外,本综述强调了特定突变(如TP53缺失)的预后意义,并探索了一些针对这些分子特征的潜在靶向治疗方法。研究结果突出了基因组分析在胰腺癌风险评估、早期检测及个性化治疗方案设计中的重要性。总体而言,本综述对胰腺肿瘤的分子复杂性进行了全面分析,为更有效、更具针对性的治疗干预铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/36b61812a90a/cimb-46-00177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/32bff09f02f2/cimb-46-00177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/36f1516682c3/cimb-46-00177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/36b61812a90a/cimb-46-00177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/32bff09f02f2/cimb-46-00177-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/36f1516682c3/cimb-46-00177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/256c/11049225/36b61812a90a/cimb-46-00177-g003.jpg

相似文献

1
Significance of TP53, CDKN2A, SMAD4 and KRAS in Pancreatic Cancer.TP53、CDKN2A、SMAD4和KRAS在胰腺癌中的意义
Curr Issues Mol Biol. 2024 Mar 23;46(4):2827-2844. doi: 10.3390/cimb46040177.
2
Immunohistochemically detected expression of 3 major genes (CDKN2A/p16, TP53, and SMAD4/DPC4) strongly predicts survival in patients with resectable pancreatic cancer.免疫组化检测到 3 个主要基因(CDKN2A/p16、TP53 和 SMAD4/DPC4)的表达水平强烈预测了可切除胰腺癌患者的生存情况。
Ann Surg. 2013 Aug;258(2):336-46. doi: 10.1097/SLA.0b013e3182827a65.
3
Long-term survivors of pancreatic adenocarcinoma show low rates of genetic alterations in KRAS, TP53 and SMAD4.胰腺导管腺癌的长期幸存者中 KRAS、TP53 和 SMAD4 的基因突变率较低。
Cancer Biomark. 2018 Feb 6;21(2):323-334. doi: 10.3233/CBM-170464.
4
Clinical Effect of Driver Mutations of , and in Pancreatic Cancer: A Meta-Analysis.胰腺癌中 、 和 驱动基因突变的临床效应:一项荟萃分析。
Genet Test Mol Biomarkers. 2020 Dec;24(12):777-788. doi: 10.1089/gtmb.2020.0078.
5
Pancreatic adenocarcinomas without KRAS, TP53, CDKN2A and SMAD4 mutations and CDKN2A/CDKN2B copy number alterations: a review of the genomic landscape to unveil therapeutic avenues.无 KRAS、TP53、CDKN2A 和 SMAD4 突变及 CDKN2A/CDKN2B 拷贝数改变的胰腺导管腺癌:揭示治疗途径的基因组全景回顾。
Chin Clin Oncol. 2023 Feb;12(1):2. doi: 10.21037/cco-22-108.
6
Utility of Assessing the Number of Mutated KRAS, CDKN2A, TP53, and SMAD4 Genes Using a Targeted Deep Sequencing Assay as a Prognostic Biomarker for Pancreatic Cancer.使用靶向深度测序检测评估KRAS、CDKN2A、TP53和SMAD4基因突变数量作为胰腺癌预后生物标志物的效用
Pancreas. 2017 Mar;46(3):335-340. doi: 10.1097/MPA.0000000000000760.
7
Identification of TPI1 As a potential therapeutic target in pancreatic cancer with dependency of TP53 mutation using multi-omics analysis.利用多组学分析鉴定 TPI1 作为具有 TP53 突变依赖性的胰腺癌潜在治疗靶点。
Cancer Sci. 2024 Nov;115(11):3622-3635. doi: 10.1111/cas.16302. Epub 2024 Sep 11.
8
Combination of KRAS and SMAD4 mutations in formalin-fixed paraffin-embedded tissues as a biomarker for pancreatic cancer.KRAS 和 SMAD4 基因突变联合在福尔马林固定石蜡包埋组织中作为胰腺癌的生物标志物。
Cancer Sci. 2020 Jun;111(6):2174-2182. doi: 10.1111/cas.14425. Epub 2020 May 30.
9
Genetic analyses of isolated high-grade pancreatic intraepithelial neoplasia (HG-PanIN) reveal paucity of alterations in TP53 and SMAD4.对孤立性高级别胰腺上皮内瘤变(HG-PanIN)的基因分析显示,TP53和SMAD4的改变很少。
J Pathol. 2017 May;242(1):16-23. doi: 10.1002/path.4884. Epub 2017 Mar 30.
10
Genomic sequencing of key genes in mouse pancreatic cancer cells.对小鼠胰腺癌细胞中关键基因进行基因组测序。
Curr Mol Med. 2012 Mar;12(3):331-41. doi: 10.2174/156652412799218868.

引用本文的文献

1
Early Detection of Pancreatic Cancer: Current Advances and Future Opportunities.胰腺癌的早期检测:当前进展与未来机遇
Biomedicines. 2025 Jul 15;13(7):1733. doi: 10.3390/biomedicines13071733.
2
Editorial: Molecular markers for pancreatic cancers: new technologies and applications in the clinical practice.社论:胰腺癌的分子标志物:新技术及其在临床实践中的应用
Front Oncol. 2025 Jul 8;15:1651566. doi: 10.3389/fonc.2025.1651566. eCollection 2025.
3
Molecular Biomarkers for the Diagnosis and Prognostication of Pancreatic Ductal Adenocarcinoma.

本文引用的文献

1
Post-operative mortality and recurrence patterns in pancreatic cancer according to KRAS mutation and CDKN2A, p53, and SMAD4 expression.根据 KRAS 突变以及 CDKN2A、p53 和 SMAD4 表达情况评估胰腺癌患者的术后死亡率和复发模式。
J Pathol Clin Res. 2023 Sep;9(5):339-353. doi: 10.1002/cjp2.323. Epub 2023 Jun 8.
2
Comprehensive analyses of cuproptosis-related gene CDKN2A on prognosis and immunologic therapy in human tumors.全面分析铜死亡相关基因 CDKN2A 对人类肿瘤预后和免疫治疗的影响。
Medicine (Baltimore). 2023 Apr 7;102(14):e33468. doi: 10.1097/MD.0000000000033468.
3
Pancreatic adenocarcinomas without KRAS, TP53, CDKN2A and SMAD4 mutations and CDKN2A/CDKN2B copy number alterations: a review of the genomic landscape to unveil therapeutic avenues.
用于胰腺导管腺癌诊断和预后评估的分子生物标志物
J Pers Med. 2025 Jun 5;15(6):236. doi: 10.3390/jpm15060236.
4
Advances in the application of extracellular vesicles in precise diagnosis of pancreatic cancer.细胞外囊泡在胰腺癌精准诊断中的应用进展
Eur J Med Res. 2025 Jun 13;30(1):478. doi: 10.1186/s40001-025-02739-5.
5
The role of HSPB1 in modulating ferroptosis in pancreatic cancer via the TP53/SLC7A11/GPX4 axis.HSPB1通过TP53/SLC7A11/GPX4轴在调节胰腺癌铁死亡中的作用。
Discov Oncol. 2025 Jun 12;16(1):1076. doi: 10.1007/s12672-025-02803-w.
6
Tumor-associated macrophages (TAMs): Constructing an immunosuppressive microenvironment bridge for pancreatic ductal adenocarcinoma (PDAC).肿瘤相关巨噬细胞(TAMs):为胰腺导管腺癌(PDAC)构建免疫抑制微环境桥梁
Cancer Pathog Ther. 2024 Jul 23;3(3):183-196. doi: 10.1016/j.cpt.2024.07.004. eCollection 2025 May.
7
Unraveling the therapeutic landscape of miRNAs in pancreatic cancer.解析胰腺癌中微小RNA的治疗前景
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jun 2. doi: 10.1007/s00210-025-04301-w.
8
Recent Advances and Challenges in the Treatment of Advanced Pancreatic Cancer: An Update on Completed and Ongoing Clinical Trials.晚期胰腺癌治疗的最新进展与挑战:已完成及正在进行的临床试验综述
Cancers (Basel). 2025 Apr 14;17(8):1319. doi: 10.3390/cancers17081319.
9
Mechanistic insights and therapeutic strategies for targeting autophagy in pancreatic ductal adenocarcinoma.胰腺导管腺癌中靶向自噬的机制见解与治疗策略
Discov Oncol. 2025 Apr 23;16(1):592. doi: 10.1007/s12672-025-02400-x.
10
Advances in Non-Invasive Screening Methods for Gastrointestinal Cancers: How Continued Innovation Has Revolutionized Early Cancer Detection.胃肠道癌症非侵入性筛查方法的进展:持续创新如何彻底改变早期癌症检测
Cancers (Basel). 2025 Mar 24;17(7):1085. doi: 10.3390/cancers17071085.
无 KRAS、TP53、CDKN2A 和 SMAD4 突变及 CDKN2A/CDKN2B 拷贝数改变的胰腺导管腺癌:揭示治疗途径的基因组全景回顾。
Chin Clin Oncol. 2023 Feb;12(1):2. doi: 10.21037/cco-22-108.
4
Multifaceted role for p53 in pancreatic cancer suppression.p53 在胰腺癌抑制中的多效性作用。
Proc Natl Acad Sci U S A. 2023 Mar 7;120(10):e2211937120. doi: 10.1073/pnas.2211937120. Epub 2023 Feb 27.
5
Cost-effectiveness of pancreas surveillance: The CDKN2A-p16-Leiden cohort.胰腺监测的成本效益:CDKN2A-p16-Leiden 队列研究。
United European Gastroenterol J. 2023 Mar;11(2):163-170. doi: 10.1002/ueg2.12360. Epub 2023 Feb 13.
6
Elucidation of the Role of SMAD4 in Epithelial-Mesenchymal Plasticity: Does It Help to Better Understand the Consequences of Inactivation in the Malignant Progression of Pancreatic Ductal Adenocarcinoma?阐明SMAD4在上皮-间质可塑性中的作用:这是否有助于更好地理解其失活在胰腺导管腺癌恶性进展中的后果?
Cancers (Basel). 2023 Jan 18;15(3):581. doi: 10.3390/cancers15030581.
7
Cancer statistics, 2023.癌症统计数据,2023 年。
CA Cancer J Clin. 2023 Jan;73(1):17-48. doi: 10.3322/caac.21763.
8
Effects of TP53 Mutations and miRs on Immune Responses in the Tumor Microenvironment Important in Pancreatic Cancer Progression.TP53 突变和 miR 对胰腺癌进展中肿瘤微环境免疫反应的影响。
Cells. 2022 Jul 9;11(14):2155. doi: 10.3390/cells11142155.
9
Wild type and gain of function mutant TP53 can regulate the sensitivity of pancreatic cancer cells to chemotherapeutic drugs, EGFR/Ras/Raf/MEK, and PI3K/mTORC1/GSK-3 pathway inhibitors, nutraceuticals and alter metabolic properties.野生型和功能获得性突变 TP53 可以调节胰腺癌细胞对化疗药物、EGFR/Ras/Raf/MEK 和 PI3K/mTORC1/GSK-3 通路抑制剂、营养保健品的敏感性,并改变代谢特性。
Aging (Albany NY). 2022 Apr 27;14(8):3365-3386. doi: 10.18632/aging.204038.
10
Molecular Characterization of KRAS Wild-type Tumors in Patients with Pancreatic Adenocarcinoma.KRAS 野生型胰腺腺癌患者的分子特征。
Clin Cancer Res. 2022 Jun 13;28(12):2704-2714. doi: 10.1158/1078-0432.CCR-21-3581.