• 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

具有增强转移潜能的癌症干细胞作为食管癌的治疗靶点。

Cancer stem cells with increased metastatic potential as a therapeutic target for esophageal cancer.

机构信息

Department of Cell Biology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands; Department of Radiation Oncology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands; Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands.

Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands.

出版信息

Semin Cancer Biol. 2017 Jun;44:60-66. doi: 10.1016/j.semcancer.2017.03.010. Epub 2017 Mar 30.

DOI:10.1016/j.semcancer.2017.03.010
PMID:28366541
Abstract

Esophageal cancers (EC) are highly aggressive tumors, commonly presented in a locally advanced stage with a poor prognosis and survival. Up to 50% of the patients are eligible for treatment with curative intent and receive the standard treatment with neoadjuvant chemoradiotherapy (nCRT) and surgery. Currently, pathologic complete response to nCRT is 20-30%, with a partial or no response in about 50% and 20%, respectively. EC recurrences occur frequently even after successful anti-cancer treatment, suggesting high aggressiveness with increased metastatic potential. A tumor sub-population of so-called cancer stem cells (CSCs), is known to display a high metastatic potential and resistance to conventional anti-cancer therapy, hereby being responsible for the unbeneficial clinical features. In this review, a concise overview will be given of the current literature on esophageal CSCs and related metastases. Esophageal CSC markers will be discussed followed by the pathways that initiate and sustain these cells. In addition, the cellular processes, epithelial-mesenchymal transition (EMT), hypoxia and autophagy, known to contribute to cancer stemness and metastasis will be explained. Finally, potential options for treatment also related to cancer genome atlas (TCGA) data on EC will be discussed.

摘要

食管癌(EC)是高度侵袭性的肿瘤,通常处于局部晚期,预后和生存率较差。多达 50%的患者有资格接受以治愈为目的的治疗,并接受新辅助放化疗(nCRT)和手术的标准治疗。目前,nCRT 的病理完全缓解率为 20-30%,部分缓解或无缓解率分别约为 50%和 20%。即使在成功的抗癌治疗后,食管癌仍经常复发,这表明其具有较高的侵袭性和转移潜能。所谓的癌症干细胞(CSC)的肿瘤亚群,已知具有较高的转移潜能和对常规抗癌治疗的耐药性,因此是导致不良临床特征的原因。在这篇综述中,将简要概述目前关于食管 CSC 及其相关转移的文献。将讨论食管 CSC 标志物,然后是启动和维持这些细胞的途径。此外,还将解释已知有助于癌症干细胞特性和转移的细胞过程,上皮-间充质转化(EMT)、缺氧和自噬。最后,还将讨论与食管癌癌症基因组图谱(TCGA)数据相关的潜在治疗选择。

相似文献

1
Cancer stem cells with increased metastatic potential as a therapeutic target for esophageal cancer.具有增强转移潜能的癌症干细胞作为食管癌的治疗靶点。
Semin Cancer Biol. 2017 Jun;44:60-66. doi: 10.1016/j.semcancer.2017.03.010. Epub 2017 Mar 30.
2
18F-FDG PET-CT after Neoadjuvant Chemoradiotherapy in Esophageal Cancer Patients to Optimize Surgical Decision Making.新辅助放化疗后18F-FDG PET-CT在食管癌患者中的应用以优化手术决策
PLoS One. 2015 Nov 3;10(11):e0133690. doi: 10.1371/journal.pone.0133690. eCollection 2015.
3
EMT, CTCs and CSCs in tumor relapse and drug-resistance.肿瘤复发和耐药中的上皮-间质转化、循环肿瘤细胞和癌症干细胞
Oncotarget. 2015 May 10;6(13):10697-711. doi: 10.18632/oncotarget.4037.
4
[Biomarkers of predicting response to neoadjuvant chemoradiotherapy in esophageal cancer].[预测食管癌新辅助放化疗反应的生物标志物]
Zhonghua Wei Chang Wai Ke Za Zhi. 2013 Sep;16(9):805-10.
5
Linking Cancer Stem Cell Plasticity to Therapeutic Resistance-Mechanism and Novel Therapeutic Strategies in Esophageal Cancer.将癌症干细胞可塑性与治疗抵抗机制相关联——食管癌的治疗策略新方向。
Cells. 2020 Jun 17;9(6):1481. doi: 10.3390/cells9061481.
6
Gli1, a potential regulator of esophageal cancer stem cell, is identified as an independent adverse prognostic factor in esophageal squamous cell carcinoma.Gli1作为食管癌干细胞的潜在调节因子,被确定为食管鳞状细胞癌的独立不良预后因素。
J Cancer Res Clin Oncol. 2017 Feb;143(2):243-254. doi: 10.1007/s00432-016-2273-6. Epub 2016 Sep 28.
7
Targeting carbonic anhydrase IX depletes breast cancer stem cells within the hypoxic niche.靶向碳酸酐酶 IX 可耗竭乏氧微环境中的乳腺癌干细胞。
Oncogene. 2013 Oct 31;32(44):5210-9. doi: 10.1038/onc.2012.550. Epub 2012 Dec 3.
8
Esophageal Adenocarcinoma Cells and Xenograft Tumors Exposed to Erb-b2 Receptor Tyrosine Kinase 2 and 3 Inhibitors Activate Transforming Growth Factor Beta Signaling, Which Induces Epithelial to Mesenchymal Transition.食管腺癌细胞和异种移植肿瘤暴露于表皮生长因子受体酪氨酸激酶 2 和 3 抑制剂可激活转化生长因子-β 信号通路,从而诱导上皮间质转化。
Gastroenterology. 2017 Jul;153(1):63-76.e14. doi: 10.1053/j.gastro.2017.03.004. Epub 2017 Mar 9.
9
The Role of Cancer Stem Cells in Recurrent and Drug-Resistant Lung Cancer.癌症干细胞在复发性和耐药性肺癌中的作用
Adv Exp Med Biol. 2016;890:57-74. doi: 10.1007/978-3-319-24932-2_4.
10
CCL21/CCR7 Axis Contributed to CD133+ Pancreatic Cancer Stem-Like Cell Metastasis via EMT and Erk/NF-κB Pathway.CCL21/CCR7轴通过上皮-间质转化和Erk/核因子κB通路促进CD133+胰腺癌干细胞样细胞转移。
PLoS One. 2016 Aug 9;11(8):e0158529. doi: 10.1371/journal.pone.0158529. eCollection 2016.

引用本文的文献

1
Integration of single-cell and bulk RNA sequencing to identify unique tumor stem cells and construct novel prognostic markers for assessing ESCA prognosis and drug sensitivity.整合单细胞和批量RNA测序以鉴定独特的肿瘤干细胞并构建用于评估食管癌预后和药物敏感性的新型预后标志物。
Front Oncol. 2025 Aug 27;15:1649877. doi: 10.3389/fonc.2025.1649877. eCollection 2025.
2
Chromatin Remodeler RSF1 as an Oncogenic Driver and Therapeutic Target in Esophageal Squamous Cell Carcinoma.染色质重塑因子RSF1作为食管鳞状细胞癌的致癌驱动因子和治疗靶点
Cells. 2025 Aug 15;14(16):1262. doi: 10.3390/cells14161262.
3
Real-world first-line serplulimab therapy for advanced esophageal cancer: effectiveness, safety, and clinical implications.
真实世界中晚期食管癌一线斯鲁利单抗治疗:疗效、安全性及临床意义
Front Med (Lausanne). 2025 Aug 6;12:1637458. doi: 10.3389/fmed.2025.1637458. eCollection 2025.
4
Key roles of ubiquitination in regulating critical regulators of cancer stem cell functionality.泛素化在调节癌症干细胞功能的关键调节因子中的关键作用。
Genes Dis. 2024 Apr 17;12(3):101311. doi: 10.1016/j.gendis.2024.101311. eCollection 2025 May.
5
Competing endogenous RNAs regulatory crosstalk networks: The messages from the RNA world to signaling pathways directing cancer stem cell development.竞争性内源RNA调控互作网络:从RNA世界到指导癌症干细胞发育的信号通路的信息
Heliyon. 2024 Jul 26;10(15):e35208. doi: 10.1016/j.heliyon.2024.e35208. eCollection 2024 Aug 15.
6
DNA polymerase iota promotes EMT and metastasis of esophageal squamous cell carcinoma by interacting with USP7 to stabilize HIF-1α.DNA 聚合酶iota 通过与 USP7 相互作用稳定 HIF-1α 促进食管鳞癌 EMT 和转移。
Cell Death Dis. 2024 Feb 24;15(2):171. doi: 10.1038/s41419-024-06552-6.
7
Prognostic value of Mandard score and nodal status for recurrence patterns and survival after multimodal treatment of oesophageal adenocarcinoma.多模式治疗食管腺癌后 Mandard 评分和淋巴结状态对复发模式和生存的预后价值。
Br J Surg. 2024 Jan 31;111(2). doi: 10.1093/bjs/znae034.
8
Potential markers of cancer stem-like cells in ESCC: a review of the current knowledge.食管癌中癌症干细胞样细胞的潜在标志物:当前知识综述
Front Oncol. 2024 Jan 4;13:1324819. doi: 10.3389/fonc.2023.1324819. eCollection 2023.
9
Engineered hydrogel reveals contribution of matrix mechanics to esophageal adenocarcinoma and identifies matrix-activated therapeutic targets.工程化水凝胶揭示了基质力学对食管腺癌的贡献,并确定了基质激活的治疗靶点。
J Clin Invest. 2023 Dec 1;133(23):e168146. doi: 10.1172/JCI168146.
10
Circ-FNDC3B Functions as an Oncogenic Factor in Esophageal Squamous Cell Carcinoma via Upregulating MYO5A by Absorbing miR-136-5p and miR-370-3p.环状结构 FNDC3B 通过吸附 miR-136-5p 和 miR-370-3p 上调 MYO5A 在食管鳞癌中发挥致癌因子的作用。
Biochem Genet. 2023 Oct;61(5):1917-1936. doi: 10.1007/s10528-023-10354-4. Epub 2023 Mar 8.