• 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

胰腺癌干细胞:对胰腺癌治疗的启示

Pancreatic cancer stem cells: implications for the treatment of pancreatic cancer.

作者信息

Simeone Diane M

机构信息

University of Michigan, Ann Arbor, Michigan 48109, USA.

出版信息

Clin Cancer Res. 2008 Sep 15;14(18):5646-8. doi: 10.1158/1078-0432.CCR-08-0584.

DOI:10.1158/1078-0432.CCR-08-0584
PMID:18794070
Abstract

Pancreatic cancer is a highly lethal disease that is usually diagnosed at a late stage for which there are few effective therapies. Emerging evidence has suggested that malignant tumors are quite heterogeneous and that they are composed of a small subset of distinct cancer cells (usually defined by cell surface marker expression) that are responsible for tumor initiation and propagation, termed cancer stem cells. These cells are termed cancer stem cells because, like normal stem cells, they possess the ability to self-renew and make differentiated progeny. Recent studies of human pancreatic cancers have shown a population of pancreatic cancer stem cells that have aberrantly activated developmental signaling pathways, are resistant to standard chemotherapy and radiation, and have up-regulated signaling cascades that are integral for tumor metastasis. An improved understanding of the biological behavior of these cells may lead to more effective therapies to treat pancreatic cancer. In this review, approaches to develop and test therapeutics targeting pancreatic cancer stem cells are discussed.

摘要

胰腺癌是一种高度致命的疾病,通常在晚期才被诊断出来,而针对晚期胰腺癌几乎没有有效的治疗方法。新出现的证据表明,恶性肿瘤具有高度异质性,由一小部分不同的癌细胞(通常根据细胞表面标志物表达来定义)组成,这些癌细胞负责肿瘤的起始和增殖,被称为癌症干细胞。这些细胞之所以被称为癌症干细胞,是因为它们与正常干细胞一样,具有自我更新和产生分化后代的能力。最近对人类胰腺癌的研究表明,存在一群胰腺癌干细胞,它们异常激活了发育信号通路,对标准化疗和放疗具有抗性,并且上调了对肿瘤转移至关重要的信号级联反应。对这些细胞生物学行为的更好理解可能会带来更有效的胰腺癌治疗方法。在这篇综述中,将讨论开发和测试针对胰腺癌干细胞的治疗方法。

相似文献

1
Pancreatic cancer stem cells: implications for the treatment of pancreatic cancer.胰腺癌干细胞:对胰腺癌治疗的启示
Clin Cancer Res. 2008 Sep 15;14(18):5646-8. doi: 10.1158/1078-0432.CCR-08-0584.
2
Identification of human pancreatic cancer stem cells.人胰腺癌干细胞的鉴定。
Methods Mol Biol. 2009;568:161-73. doi: 10.1007/978-1-59745-280-9_10.
3
Targeting cancer stem cells for more effective therapies: Taking out cancer's locomotive engine.靶向癌症干细胞以实现更有效的治疗:摘除癌症的动力引擎。
Biochem Pharmacol. 2009 Aug 15;78(4):326-34. doi: 10.1016/j.bcp.2009.03.020. Epub 2009 Apr 1.
4
Pancreatic cancer stem cells and relevance to cancer treatments.胰腺癌干细胞及其与癌症治疗的相关性。
J Cell Biochem. 2009 May 1;107(1):40-5. doi: 10.1002/jcb.22093.
5
Cancer stem cells in solid tumors.实体瘤中的癌症干细胞。
Onkologie. 2009 Oct;32(10):605-9. doi: 10.1159/000232375. Epub 2009 Sep 14.
6
Do stem-like cells play a role in drug resistance of sarcomas?干细胞在肉瘤的耐药中发挥作用吗?
Expert Rev Anticancer Ther. 2010 Feb;10(2):261-70. doi: 10.1586/era.09.184.
7
Pancreatic cancer stem cells--insights and perspectives.胰腺癌干细胞——见解与展望
Expert Opin Biol Ther. 2009 Oct;9(10):1271-8. doi: 10.1517/14712590903246362.
8
Cancer, stem cells, and oncolytic viruses.癌症、干细胞与溶瘤病毒。
Ann Med. 2008;40(7):496-505. doi: 10.1080/07853890802021342.
9
Metastatic activity and chemotherapy resistance in human pancreatic cancer--influence of cancer stem cells.人胰腺癌中的转移活性与化疗耐药性——癌症干细胞的影响
Surgery. 2009 Sep;146(3):430-4. doi: 10.1016/j.surg.2009.05.003. Epub 2009 Jun 25.
10
Cancer stem cells: an old idea--a paradigm shift.癌症干细胞:一个古老的概念——一场范式转变。
Cancer Res. 2006 Feb 15;66(4):1883-90; discussion 1895-6. doi: 10.1158/0008-5472.CAN-05-3153.

引用本文的文献

1
Therapeutic potential of flavonoids in gastrointestinal cancer: Focus on signaling pathways and improvement strategies (Review).黄酮类化合物在胃肠道癌中的治疗潜力:聚焦信号通路及改善策略(综述)
Mol Med Rep. 2025 Apr;31(4). doi: 10.3892/mmr.2025.13474. Epub 2025 Feb 28.
2
The p53 reactivator PRIMA-1 synergises with 5-fluorouracil to induce apoptosis in pancreatic cancer cells.p53 再激活剂 PRIMA-1 与 5-氟尿嘧啶协同诱导胰腺癌细胞凋亡。
Invest New Drugs. 2023 Aug;41(4):587-595. doi: 10.1007/s10637-023-01380-5. Epub 2023 Jul 4.
3
Recent advance of herbal medicines in cancer- a molecular approach.
草药在癌症治疗中的最新进展——分子学方法
Heliyon. 2023 Feb 14;9(2):e13684. doi: 10.1016/j.heliyon.2023.e13684. eCollection 2023 Feb.
4
Resistance to Gemcitabine in Pancreatic Ductal Adenocarcinoma: A Physiopathologic and Pharmacologic Review.胰腺导管腺癌对吉西他滨的耐药性:生理病理学与药理学综述
Cancers (Basel). 2022 May 18;14(10):2486. doi: 10.3390/cancers14102486.
5
Induction of Apoptosis in Human Pancreatic Cancer Stem Cells by the Endoplasmic Reticulum-Targeted Alkylphospholipid Analog Edelfosine and Potentiation by Autophagy Inhibition.内质网靶向烷基磷脂类似物依地福新诱导人胰腺癌干细胞凋亡及自噬抑制的增强作用
Cancers (Basel). 2021 Dec 5;13(23):6124. doi: 10.3390/cancers13236124.
6
Engineering of a functional pancreatic acinus with reprogrammed cancer cells by induced expression.通过诱导表达工程化具有重编程癌细胞功能的胰腺腺泡
Lab Chip. 2021 Sep 28;21(19):3675-3685. doi: 10.1039/d1lc00350j.
7
Inflammation, Extracellular Matrix Remodeling, and Proteostasis in Tumor Microenvironment.肿瘤微环境中的炎症、细胞外基质重塑和蛋白质稳态
Int J Mol Sci. 2021 Jul 28;22(15):8102. doi: 10.3390/ijms22158102.
8
Transcriptomic Profiling Identifies DCBLD2 as a Diagnostic and Prognostic Biomarker in Pancreatic Ductal Adenocarcinoma.转录组分析确定DCBLD2为胰腺导管腺癌的诊断和预后生物标志物。
Front Mol Biosci. 2021 Mar 23;8:659168. doi: 10.3389/fmolb.2021.659168. eCollection 2021.
9
Development and validation of a cancer stem cell-related signature for prognostic prediction in pancreatic ductal adenocarcinoma.用于预测胰腺导管腺癌预后的癌症干细胞相关特征的开发与验证
J Transl Med. 2020 Sep 21;18(1):360. doi: 10.1186/s12967-020-02527-1.
10
Upregulation of DUSP14 Affects Proliferation, Invasion and Metastasis, Potentially via Epithelial-Mesenchymal Transition and Is Associated with Poor Prognosis in Pancreatic Cancer.DUSP14的上调可能通过上皮-间质转化影响增殖、侵袭和转移,并与胰腺癌的不良预后相关。
Cancer Manag Res. 2020 Mar 20;12:2097-2108. doi: 10.2147/CMAR.S240040. eCollection 2020.