Ardelt Barbara, Ardelt Wojciech, Pozarowski Piotr, Kunicki Jan, Shogen Kuslima, Darzynkiewicz Zbigniew
Brander Cancer Research Institute and Department of Pathology, New York Medical College, Valhalla, New York 10595, USA.
Cell Cycle. 2007 Dec 15;6(24):3097-102. doi: 10.4161/cc.6.24.5045. Epub 2007 Sep 12.
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.
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。