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小干扰RNA和脱氧核酶在癌症治疗中的潜力

Therapeutic potential of siRNA and DNAzymes in cancer.

作者信息

Karnati Hanuma Kumar, Yalagala Ravi Shekar, Undi Rambabu, Pasupuleti Satya Ratan, Gutti Ravi Kumar

机构信息

Hematologic Oncology, Stem Cells and Blood Disorders Laboratory, Department of Biochemistry, School of Life Sciences, University of Hyderabad, (PO) Gachibowli, Hyderabad, AP, 500046, India.

出版信息

Tumour Biol. 2014 Oct;35(10):9505-21. doi: 10.1007/s13277-014-2477-9. Epub 2014 Aug 23.

DOI:10.1007/s13277-014-2477-9
PMID:25149153
Abstract

Cancer is characterized by uncontrolled cell growth, invasion, and metastasis and possess threat to humans worldwide. The scientific community is facing numerous challenges despite several efforts to cure cancer. Though a number of studies were done earlier, the molecular mechanism of cancer progression is not completely understood. Currently available treatments like surgery resection, adjuvant chemotherapy, and radiotherapy are not completely effective in curing all the cancers. Recent advances in the antisense technology provide a powerful tool to investigate various cancer pathways and target them. Small interfering RNAs (siRNAs) could be effective in downregulating the cancer-associated genes, but their in vivo delivery is the main obstacle. DNA enzymes (DNAzymes) have great potential in the treatment of cancer due to high selectivity and significant catalytic efficiency. In this review, we are focusing on antisense molecules such as siRNA and DNAzymes in cancer therapeutics development. This review also describes the challenges and approaches to overcome obstacles involved in using siRNA and DNAzymes in the treatment of cancers.

摘要

癌症的特征是细胞不受控制地生长、侵袭和转移,对全球人类构成威胁。尽管科学界为治愈癌症付出了诸多努力,但仍面临众多挑战。虽然此前已开展了大量研究,但癌症进展的分子机制尚未完全明晰。目前可用的治疗方法,如手术切除、辅助化疗和放疗,在治愈所有癌症方面并不完全有效。反义技术的最新进展为研究各种癌症途径并靶向这些途径提供了有力工具。小干扰RNA(siRNA)在下调癌症相关基因方面可能有效,但其体内递送是主要障碍。DNA酶(脱氧核酶)由于具有高选择性和显著的催化效率,在癌症治疗中具有巨大潜力。在本综述中,我们重点关注癌症治疗发展中的反义分子,如siRNA和DNA酶。本综述还描述了在癌症治疗中使用siRNA和DNA酶所涉及的挑战以及克服障碍的方法。

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Therapeutic potential of siRNA and DNAzymes in cancer.小干扰RNA和脱氧核酶在癌症治疗中的潜力
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2
DNAzymes as potential therapeutic molecules.脱氧核酶作为潜在的治疗分子。
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DNAzyme loaded nano-niosomes attenuate myocardial ischemia/reperfusion injury by targeting apoptosis, inflammation in a NF-κB dependent mechanism.载有 DNA 酶的纳米奈莫体通过靶向细胞凋亡、炎症反应NF-κB 依赖机制减轻心肌缺血/再灌注损伤。
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本文引用的文献

1
Fluorescence visualization screening for EBV-LMP1-targeted DNAzymes.荧光可视化筛选 EBV-LMP1 靶向 DNA 酶。
Otolaryngol Head Neck Surg. 2014 Feb;150(2):251-8. doi: 10.1177/0194599813514514. Epub 2013 Dec 9.
2
Antiangiogenic and antitumoral effects mediated by a vascular endothelial growth factor receptor 1 (VEGFR-1)-targeted DNAzyme.血管内皮生长因子受体1(VEGFR-1)靶向脱氧核酶介导的抗血管生成和抗肿瘤作用
Mol Med. 2013 Nov 8;19(1):377-86. doi: 10.2119/molmed.2013.00090.
3
The siRNA cocktail targeting VEGF and HER2 inhibition on the proliferation and induced apoptosis of gastric cancer cell.
一种用于触发基因光动力调节扩增的动态DNA纳米海绵。
Chem Sci. 2022 Mar 28;13(18):5155-5163. doi: 10.1039/d2sc00459c. eCollection 2022 May 11.
4
Recent advances in functionalized upconversion nanoparticles for light-activated tumor therapy.用于光激活肿瘤治疗的功能化上转换纳米粒子的最新进展
RSC Adv. 2021 Nov 3;11(56):35472-35488. doi: 10.1039/d1ra05638g. eCollection 2021 Oct 28.
5
DNAzymes, Novel Therapeutic Agents in Cancer Therapy: A Review of Concepts to Applications.DNA 酶:癌症治疗中的新型治疗剂——从概念到应用的综述
J Nucleic Acids. 2021 Nov 1;2021:9365081. doi: 10.1155/2021/9365081. eCollection 2021.
6
Targeted and direct intracellular delivery of native DNAzymes enables highly specific gene silencing.天然脱氧核酶的靶向性和直接细胞内递送可实现高度特异性的基因沉默。
Chem Sci. 2020 Aug 7;11(33):8966-8972. doi: 10.1039/d0sc03974h.
7
Fluorescence Based Investigation of Temperature-Dependent Pb-Specific 8-17E DNAzyme Catalytic Sensor.基于荧光的温度依赖型 Pb 特异性 8-17E DNA zyme 催化传感器研究。
J Fluoresc. 2019 Mar;29(2):335-342. doi: 10.1007/s10895-019-02346-8. Epub 2019 Feb 18.
8
Theranostic DNAzymes.诊疗性脱氧核酶
Theranostics. 2017 Feb 23;7(4):1010-1025. doi: 10.7150/thno.17736. eCollection 2017.
9
Thirty-five years of research into ribozymes and nucleic acid catalysis: where do we stand today?对核酶和核酸催化作用的35年研究:我们如今处于什么阶段?
F1000Res. 2016 Jun 27;5. doi: 10.12688/f1000research.8601.1. eCollection 2016.
10
Platelet-derived growth factor receptor/platelet-derived growth factor (PDGFR/PDGF) system is a prognostic and treatment response biomarker with multifarious therapeutic targets in cancers.血小板衍生生长因子受体/血小板衍生生长因子(PDGFR/PDGF)系统是一种癌症预后和治疗反应生物标志物,在癌症中有多种治疗靶点。
Tumour Biol. 2016 Aug;37(8):10053-66. doi: 10.1007/s13277-016-5069-z. Epub 2016 May 19.
针对血管内皮生长因子和人表皮生长因子受体 2 的 siRNA 鸡尾酒抑制胃癌细胞的增殖并诱导其凋亡。
Mol Cell Biochem. 2014 Jan;386(1-2):117-24. doi: 10.1007/s11010-013-1850-0. Epub 2013 Oct 26.
4
Targeting EBV-LMP1 DNAzyme enhances radiosensitivity of nasopharyngeal carcinoma cells by inhibiting telomerase activity.靶向EBV-LMP1脱氧核酶通过抑制端粒酶活性增强鼻咽癌细胞的放射敏感性。
Cancer Biol Ther. 2014 Jan;15(1):61-8. doi: 10.4161/cbt.26606. Epub 2013 Oct 21.
5
Combination of siRNA-directed Gene Silencing With Cisplatin Reverses Drug Resistance in Human Non-small Cell Lung Cancer.siRNA 介导的基因沉默联合顺铂逆转人非小细胞肺癌耐药。
Mol Ther Nucleic Acids. 2013 Jul 30;2(7):e110. doi: 10.1038/mtna.2013.29.
6
Intravenous delivery of siRNA targeting CD47 effectively inhibits melanoma tumor growth and lung metastasis.静脉注射靶向 CD47 的 siRNA 可有效抑制黑色素瘤肿瘤生长和肺转移。
Mol Ther. 2013 Oct;21(10):1919-29. doi: 10.1038/mt.2013.135. Epub 2013 Jun 18.
7
AKT1 inhibitory DNAzymes inhibit cell proliferation and migration of thyroid cancer cells.AKT1抑制性脱氧核酶抑制甲状腺癌细胞的增殖和迁移。
Asian Pac J Cancer Prev. 2013;14(4):2571-5. doi: 10.7314/apjcp.2013.14.4.2571.
8
5'-triphosphate-siRNA against survivin gene induces interferon production and inhibits proliferation of lung cancer cells in vitro.针对生存素基因的 5′-三磷酸化 siRNA 可诱导干扰素产生并抑制肺癌细胞体外增殖。
J Immunother. 2013 Jun;36(5):294-304. doi: 10.1097/CJI.0b013e318294183b.
9
Gene silencing with siRNA targeting E6/E7 as a therapeutic intervention against head and neck cancer-containing HPV16 cell lines.使用靶向E6/E7的小干扰RNA(siRNA)进行基因沉默作为针对含人乳头瘤病毒16型(HPV16)的头颈癌细胞系的一种治疗干预措施。
Acta Otolaryngol. 2013 Jul;133(7):761-71. doi: 10.3109/00016489.2013.773405. Epub 2013 May 3.
10
Distinct inhibitory efficiency of siRNAs and DNAzymes to β1 integrin subunit in blocking tumor growth.小干扰RNA(siRNAs)和脱氧核酶对β1整合素亚基在阻断肿瘤生长方面的不同抑制效率。
Acta Biochim Pol. 2013;60(1):77-82. Epub 2013 Mar 19.