Bataticola Rhizoctonia凝集素(RBL)诱导人卵巢癌PA-1细胞凋亡并抑制肿瘤生长的实验研究

Sachin M. Eligar, R. Pujari, Mohammed Azharuddin Savanur, Nagaraja N. Nagre, Srikanth Barkeer, A. Ingle, R. Kalraiya, Bale M. Swamy, P. Shastry, S. Inamdar
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引用次数: 9

摘要

背景:一种来自植物病原真菌bataticola Rhizoctonia (RBL)的凝集素对n -聚糖复合物显示出独特的糖结合特异性,已知n -聚糖复合物在包括卵巢癌在内的许多癌症中表达。先前的研究表明RBL对人卵巢癌PA-1细胞具有细胞毒性作用。在本研究中,我们确定了RBL与细胞表面受体结合后在PA-1细胞中诱导细胞毒性的信号传导机制,并评估了RBL在卵巢异种移植NOD-SCID小鼠中的抗肿瘤活性。方法:采用MTT法检测细胞毒性、细胞周期分析、Annexin V染色、流式细胞术检测caspase-3的表达。Western blotting观察凋亡通路的中间产物。结果:RBL治疗PA-1细胞后,其细胞活力呈剂量和时间依赖性降低。细胞周期分析显示,在响应凝集素处理下,次二倍体群体增加。膜联蛋白V和PI染色显示rbl处理细胞的早期和晚期凋亡群体均增加。rbl诱导PA-1细胞凋亡的机制通过观察MMP的降低(ΔΨm)、细胞色素c的释放、caspase-9和-3的激活以及PARP的裂解来评估。特异性药物抑制剂显示caspase-9和-3参与,而caspase-8不参与。亚毒性浓度(50 μg/只)的RBL可抑制PA-1异种移植NOD-SCID小鼠的肿瘤生长。结论:本研究表明RBL对PA-1细胞的细胞毒性是通过内在凋亡途径介导的。本研究加强了RBL在卵巢癌研究中的潜在应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhizoctonia Bataticola Lectin (RBL) Induces Apoptosis in Human Ovarian Cancer PA-1 Cells and Suppresses Tumor Growth In Vivo
Background: A lectin from the plant pathogenic fungus Rhizoctonia bataticola (RBL) has shown unique sugarbinding specificity towards the complex N-glycans, which are known to be expressed in many cancers, including ovarian cancer. Previous studies have demonstrated that RBL exerts cytotoxic effects on human ovarian cancer PA-1 cells. In the present study, we determined the signaling mechanism of RBL-induced cytotoxicity in PA-1 cells upon binding to cell surface receptors and also assessed the anti-tumor activity of RBL in NOD-SCID mice bearing ovarian xenografts. Methods: Cytotoxicity was determined by MTT assay, Cell cycle analysis, Annexin V staining, and expression of caspase-3 was determined by flow cytometry using specific fluorescent detection reagents. Western blotting was carried out to observe the intermediates of apoptotic pathway. Results: Treatment of PA-1 cells with RBL decreased their viability in a dose- and time- dependent manner. Cell cycle analysis revealed an increase in the hypo diploid population in response to lectin treatment. RBL-treated cells stained with Annexin V and PI showed an increase in both the early and late apoptotic populations. The mechanism of RBL-induced apoptosis in PA-1 cells was assessed by the observed decrease in MMP (ΔΨm), release of cytochrome-c, activation of caspase-9 and -3, and cleavage of PARP. Specific pharmacological inhibitors revealed the involvement of caspase-9 and -3 but not caspase-8. RBL at a subtoxic concentration (50 μg/mouse) suppressed tumor growth in NOD-SCID mice bearing PA-1 xenografts. Conclusions: The present study demonstrates that, RBL induced cytotoxicity in PA-1 cells is mediated by intrinsic apoptotic pathway. The present study strengthens the merit of RBL for its potential application in ovarian cancer research.
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