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Cytostatic and cytotoxic properties of Amphinase: a novel cytotoxic ribonuclease from Rana pipiens oocytes.两栖酶的细胞生长抑制和细胞毒性特性:一种来自豹蛙卵母细胞的新型细胞毒性核糖核酸酶
Cell Cycle. 2007 Dec 15;6(24):3097-102. doi: 10.4161/cc.6.24.5045. Epub 2007 Sep 12.
2
Onconase and amphinase, the antitumor ribonucleases from Rana pipiens oocytes.豹蛙卵母细胞中的抗肿瘤核糖核酸酶——癌抑素和两栖酶。
Curr Pharm Biotechnol. 2008 Jun;9(3):215-25. doi: 10.2174/138920108784567245.
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Enzymatic and structural characterisation of amphinase, a novel cytotoxic ribonuclease from Rana pipiens oocytes.牛蛙卵母细胞中一种新型细胞毒性核糖核酸酶——两栖酶的酶学及结构特征
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Enhancement of activation-induced apoptosis of lymphocytes by the cytotoxic ribonuclease onconase (Ranpirnase).细胞毒性核糖核酸酶昂卡司他(兰吡奈酶)增强激活诱导的淋巴细胞凋亡
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The interdependence between catalytic activity, conformational stability, and cytotoxicity of onconase.癌酶的催化活性、构象稳定性和细胞毒性之间的相互依存关系。
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Cytotoxic activity of the amphibian ribonucleases onconase and r-amphinase on tumor cells from B cell lymphoproliferative disorders.
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Remarkable enhancement of cytotoxicity of onconase and cepharanthine when used in combination on various tumor cell lines.当联合使用时,抑癌酶和千金藤素对多种肿瘤细胞系的细胞毒性显著增强。
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Treatment of Jurkat acute T-lymphocytic leukemia cells by onconase (Ranpirnase) is accompanied by an altered nucleocytoplasmic distribution and reduced expression of transcription factor NF-kappaB.用核糖核酸酶(兰瑞肽酶)处理人急性T淋巴细胞白血病Jurkat细胞时,会伴随着转录因子NF-κB的核质分布改变和表达降低。
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Ribonucleases as potential modalities in anticancer therapy.核糖核酸酶作为抗癌疗法的潜在手段。
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Induction of differentiation of leukaemic (HL-60) or prostate cancer (LNCaP, JCA-1) cells potentiates apoptosis triggered by onconase.白血病(HL-60)或前列腺癌(LNCaP、JCA-1)细胞分化的诱导增强了核糖核酸酶触发的细胞凋亡。
Cell Prolif. 2000 Dec;33(6):407-17. doi: 10.1046/j.1365-2184.2000.00186.x.

引用本文的文献

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Activating transcription factor 3 is crucial for antitumor activity and to strengthen the antiviral properties of Onconase.激活转录因子3对于抗肿瘤活性以及增强昂科纳酶的抗病毒特性至关重要。
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Ribonucleases as potential modalities in anticancer therapy.核糖核酸酶作为抗癌疗法的潜在手段。
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Onconase and amphinase, the antitumor ribonucleases from Rana pipiens oocytes.豹蛙卵母细胞中的抗肿瘤核糖核酸酶——癌抑素和两栖酶。
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Barnase as a new therapeutic agent triggering apoptosis in human cancer cells.芽孢杆菌RNA酶作为一种可引发人类癌细胞凋亡的新型治疗剂。
PLoS One. 2008 Jun 18;3(6):e2434. doi: 10.1371/journal.pone.0002434.
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Remarkable enhancement of cytotoxicity of onconase and cepharanthine when used in combination on various tumor cell lines.当联合使用时,抑癌酶和千金藤素对多种肿瘤细胞系的细胞毒性显著增强。
Cancer Biol Ther. 2008 Jul;7(7):1104-8. doi: 10.4161/cbt.7.7.6172. Epub 2008 Apr 19.

本文引用的文献

1
DNA strand breaks occurring during apoptosis - their early insitu detection by the terminal deoxynucleotidyl transferase and nick translation assays and prevention by serine protease inhibitors.凋亡过程中发生的DNA链断裂——通过末端脱氧核苷酸转移酶和缺口平移分析对其进行早期原位检测以及丝氨酸蛋白酶抑制剂对其的预防。
Int J Oncol. 1992 Nov;1(6):639-48. doi: 10.3892/ijo.1.6.639.
2
Ribonucleases as novel chemotherapeutics : the ranpirnase example.核糖核酸酶作为新型化疗药物:兰瑞肽酶实例
BioDrugs. 2008;22(1):53-8. doi: 10.2165/00063030-200822010-00006.
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Binase induces apoptosis of transformed myeloid cells and does not induce T-cell immune response.Binase可诱导转化髓样细胞凋亡,且不诱导T细胞免疫反应。
Biochem Biophys Res Commun. 2007 Oct 5;361(4):1000-5. doi: 10.1016/j.bbrc.2007.07.143. Epub 2007 Aug 3.
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Relevance of microRNAs in normal and malignant development, including human testicular germ cell tumours.微小RNA在正常和恶性发育中的相关性,包括人类睾丸生殖细胞肿瘤。
Int J Androl. 2007 Aug;30(4):304-14; discussion 314-5. doi: 10.1111/j.1365-2605.2007.00765.x. Epub 2007 Jun 15.
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Enzymatic and structural characterisation of amphinase, a novel cytotoxic ribonuclease from Rana pipiens oocytes.牛蛙卵母细胞中一种新型细胞毒性核糖核酸酶——两栖酶的酶学及结构特征
J Mol Biol. 2007 Aug 3;371(1):93-111. doi: 10.1016/j.jmb.2007.04.071. Epub 2007 May 10.
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Differential regulation of microRNAs by p53 revealed by massively parallel sequencing: miR-34a is a p53 target that induces apoptosis and G1-arrest.通过大规模平行测序揭示p53对微小RNA的差异调控:miR-34a是一个诱导凋亡和G1期阻滞的p53靶标。
Cell Cycle. 2007 Jul 1;6(13):1586-93. doi: 10.4161/cc.6.13.4436. Epub 2007 May 11.
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A new paradigm for developmental biology.发育生物学的一种新范式。
J Exp Biol. 2007 May;210(Pt 9):1526-47. doi: 10.1242/jeb.005017.
8
microRNAs and cancer: role in tumorigenesis, patient classification and therapy.微小RNA与癌症:在肿瘤发生、患者分类及治疗中的作用
Clin Transl Oncol. 2007 Mar;9(3):155-60. doi: 10.1007/s12094-007-0029-0.
9
Intracellular pathway of Onconase that enables its delivery to the cytosol.癌抑素的细胞内途径,该途径使其能够被递送至胞质溶胶。
J Cell Sci. 2007 Apr 15;120(Pt 8):1405-11. doi: 10.1242/jcs.03427. Epub 2007 Mar 20.
10
Antitumor efficacy of the cytotoxic RNase, ranpirnase, on A549 human lung cancer xenografts of nude mice.细胞毒性核糖核酸酶兰瑞肽酶对裸鼠A549人肺癌异种移植瘤的抗肿瘤疗效。
Anticancer Res. 2007 Jan-Feb;27(1A):299-307.

两栖酶的细胞生长抑制和细胞毒性特性:一种来自豹蛙卵母细胞的新型细胞毒性核糖核酸酶

Cytostatic and cytotoxic properties of Amphinase: a novel cytotoxic ribonuclease from Rana pipiens oocytes.

作者信息

Ardelt Barbara, Ardelt Wojciech, Pozarowski Piotr, Kunicki Jan, Shogen Kuslima, Darzynkiewicz Zbigniew

机构信息

Brander Cancer Research Institute and Department of Pathology, New York Medical College, Valhalla, New York 10595, USA.

出版信息

Cell Cycle. 2007 Dec 15;6(24):3097-102. doi: 10.4161/cc.6.24.5045. Epub 2007 Sep 12.

DOI:10.4161/cc.6.24.5045
PMID:18073526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2586934/
Abstract

Onconase (Onc), is a novel amphibian cytotoxic ribonuclease with antitumor activity, and is currently in a confirmatory phase III clinical trial for the treatment of malignant mesothelioma. It was recently reported that Rana pipiens oocytes contain still another ribonuclease, named Amphinase (Amph). Amph shows 38-40% amino acid sequence identity with onconase, presents as four variants varying between themselves from 87-99% in amino acid sequence identity and has a molecular mass approximately 13,000. In the present study we describe the effects of Amph on growth of several tumor cell lines. All four variants demonstrated cytostatic and cytotoxic activity against human promyelocytic HL-60-, Jurkat T-cell- and U-937 monocytic leukemia cells. The pattern of Amph activity to certain extent resembled that of Onc. Thus, cell proliferation was suppressed at 0.5-10.0 mug/ml (40-80 nM) Amph concentration with distinct accumulation of cells in G(1) phase of the cell cycle. In addition, the cells were undergoing apoptosis, which manifested by DNA fragmentation (presence of "sub-G1" cells, TUNEL-positivity), caspases and serine proteases activation as well as activation of transglutaminase. The cytostatic and cytotoxic effects of Amph required its ribonuclease activity: the enzymatically inactive Amph-2 having histidine at the active site alkylated was ineffective. The effectiveness and cell cycle specificity was generally similar for all four Amph variants and at the equimolar concentrations was somewhat more pronounced than that of Onc. The observed cytostatic and cytotoxic activity of Amph against tumor cell lines suggests that similar to Onc this cytotoxic ribonuclease may have antitumor activity and find an application in clinical oncology.

摘要

癌蛙酶(Onconase,Onc)是一种具有抗肿瘤活性的新型两栖类细胞毒性核糖核酸酶,目前正处于治疗恶性间皮瘤的III期确证性临床试验阶段。最近有报道称,豹蛙卵母细胞中还含有另一种核糖核酸酶,名为安福蛙酶(Amphinase,Amph)。Amph与癌蛙酶的氨基酸序列同一性为38 - 40%,呈现为四种变体,它们之间的氨基酸序列同一性在87 - 99%之间,分子量约为13,000。在本研究中,我们描述了Amph对几种肿瘤细胞系生长的影响。所有四种变体对人早幼粒细胞HL - 60、Jurkat T细胞和U - 937单核细胞白血病细胞均表现出细胞生长抑制和细胞毒性活性。Amph活性模式在一定程度上类似于癌蛙酶。因此,在0.5 - 10.0微克/毫升(40 - 80纳摩尔)的Amph浓度下,细胞增殖受到抑制,细胞周期的G(1)期有明显的细胞积累。此外,细胞正在经历凋亡,表现为DNA片段化(“亚G1”细胞的存在、TUNEL阳性)、半胱天冬酶和丝氨酸蛋白酶激活以及转谷氨酰胺酶激活。Amph的细胞生长抑制和细胞毒性作用需要其核糖核酸酶活性:活性位点处组氨酸被烷基化的无酶活性的Amph - 2无效。所有四种Amph变体的有效性和细胞周期特异性总体相似,在等摩尔浓度下比癌蛙酶更明显。观察到的Amph对肿瘤细胞系的细胞生长抑制和细胞毒性活性表明,与癌蛙酶类似,这种细胞毒性核糖核酸酶可能具有抗肿瘤活性,并可在临床肿瘤学中得到应用。