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Discovery of Clinical Candidate BMS-906024: A Potent Pan-Notch Inhibitor for the Treatment of Leukemia and Solid Tumors.临床候选药物BMS-906024的发现:一种用于治疗白血病和实体瘤的强效泛Notch抑制剂。
ACS Med Chem Lett. 2015 Mar 11;6(5):523-7. doi: 10.1021/acsmedchemlett.5b00001. eCollection 2015 May 14.
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Wnt blockers inhibit the proliferation of lung cancer stem cells.Wnt阻断剂可抑制肺癌干细胞的增殖。
Drug Des Devel Ther. 2015 Apr 28;9:2399-407. doi: 10.2147/DDDT.S76602. eCollection 2015.
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Curcumin effectively inhibits oncogenic NF-κB signaling and restrains stemness features in liver cancer.姜黄素可有效抑制致癌性核因子-κB信号传导,并抑制肝癌中的干性特征。
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Targeting Notch signaling with a Notch2/Notch3 antagonist (tarextumab) inhibits tumor growth and decreases tumor-initiating cell frequency.靶向 Notch 信号通路的 Notch2/Notch3 拮抗剂(tarextumab)可抑制肿瘤生长并降低肿瘤起始细胞频率。
Clin Cancer Res. 2015 May 1;21(9):2084-95. doi: 10.1158/1078-0432.CCR-14-2808.
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Combined inhibition of AKT/mTOR and MDM2 enhances Glioblastoma Multiforme cell apoptosis and differentiation of cancer stem cells.联合抑制AKT/mTOR和MDM2可增强多形性胶质母细胞瘤细胞凋亡及癌症干细胞的分化。
Sci Rep. 2015 Apr 21;5:9956. doi: 10.1038/srep09956.
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Characterization of a murine model of metastatic human non-small cell lung cancer and effect of CXCR4 inhibition on the growth of metastases.转移性人类非小细胞肺癌小鼠模型的特征及CXCR4抑制对转移灶生长的影响
Oncoscience. 2015 Feb 9;2(3):263-71. doi: 10.18632/oncoscience.117. eCollection 2015.
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Concise Review: Targeting Cancer Stem Cells Using Immunologic Approaches.简要综述:利用免疫方法靶向癌症干细胞
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Carbonic anhydrase-IX score is a novel biomarker that predicts recurrence and survival for high-risk, nonmetastatic renal cell carcinoma: Data from the phase III ARISER clinical trial.碳酸酐酶IX评分是一种预测高危、非转移性肾细胞癌复发和生存情况的新型生物标志物:来自III期ARISER临床试验的数据。
Urol Oncol. 2015 May;33(5):204.e25-33. doi: 10.1016/j.urolonc.2015.02.013. Epub 2015 Mar 29.
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Angiogenesis in cancer: Anti-VEGF escape mechanisms.癌症中的血管生成:抗 VEGF 逃逸机制。
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Consequences of Disrupted Notch Signaling in Bladder Cancer. Notch 信号通路中断在膀胱癌中的后果。
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针对癌症干细胞的疗法:当前趋势与未来挑战。

Therapies targeting cancer stem cells: Current trends and future challenges.

作者信息

Dragu Denisa L, Necula Laura G, Bleotu Coralia, Diaconu Carmen C, Chivu-Economescu Mihaela

机构信息

Denisa L Dragu, Laura G Necula, Coralia Bleotu, Carmen C Diaconu, Mihaela Chivu-Economescu, Cellular and Molecular Department, Stefan S. Nicolau Institute of Virology, 030304 Bucharest, Romania.

出版信息

World J Stem Cells. 2015 Oct 26;7(9):1185-201. doi: 10.4252/wjsc.v7.i9.1185.

DOI:10.4252/wjsc.v7.i9.1185
PMID:26516409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4620424/
Abstract

Traditional therapies against cancer, chemo- and radiotherapy, have multiple limitations that lead to treatment failure and cancer recurrence. These limitations are related to systemic and local toxicity, while treatment failure and cancer relapse are due to drug resistance and self-renewal, properties of a small population of tumor cells called cancer stem cells (CSCs). These cells are involved in cancer initiation, maintenance, metastasis and recurrence. Therefore, in order to develop efficient treatments that can induce a long-lasting clinical response preventing tumor relapse it is important to develop drugs that can specifically target and eliminate CSCs. Recent identification of surface markers and understanding of molecular feature associated with CSC phenotype helped with the design of effective treatments. In this review we discuss targeting surface biomarkers, signaling pathways that regulate CSCs self-renewal and differentiation, drug-efflux pumps involved in apoptosis resistance, microenvironmental signals that sustain CSCs growth, manipulation of miRNA expression, and induction of CSCs apoptosis and differentiation, with specific aim to hamper CSCs regeneration and cancer relapse. Some of these agents are under evaluation in preclinical and clinical studies, most of them for using in combination with traditional therapies. The combined therapy using conventional anticancer drugs with CSCs-targeting agents, may offer a promising strategy for management and eradication of different types of cancers.

摘要

传统的抗癌疗法,即化疗和放疗,存在多种局限性,这些局限性会导致治疗失败和癌症复发。这些局限性与全身和局部毒性有关,而治疗失败和癌症复发则归因于耐药性和自我更新,这是一小部分被称为癌症干细胞(CSCs)的肿瘤细胞所具有的特性。这些细胞参与癌症的起始、维持、转移和复发。因此,为了开发能够诱导长期临床反应以防止肿瘤复发的有效治疗方法,开发能够特异性靶向并消除癌症干细胞的药物非常重要。最近对表面标志物的鉴定以及对与癌症干细胞表型相关分子特征的了解有助于设计有效的治疗方法。在这篇综述中,我们讨论了靶向表面生物标志物、调节癌症干细胞自我更新和分化的信号通路、参与抗凋亡的药物外排泵、维持癌症干细胞生长的微环境信号、对微小RNA表达的调控以及诱导癌症干细胞凋亡和分化,特别旨在阻碍癌症干细胞的再生和癌症复发。其中一些药物正在临床前和临床研究中进行评估,大多数是用于与传统疗法联合使用。使用传统抗癌药物与靶向癌症干细胞的药物联合治疗,可能为管理和根除不同类型的癌症提供一种有前景的策略。