Mukhopadhyay Subhadip, Panda Prashanta Kumar, Das Durgesh Nandini, Sinha Niharika, Behera Birendra, Maiti Tapas Kumar, Bhutia Sujit Kumar
Department of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Department of Biotechnology, Indian Institute of Technology, Kharagpur, West Bengal, India.
Acta Pharmacol Sin. 2014 Jun;35(6):814-24. doi: 10.1038/aps.2014.15. Epub 2014 May 5.
Abrus agglutinin (AGG) from the seeds of Indian medicinal plant Abrus precatorius belongs to the class II ribosome inactivating protein family. In this study we investigated the anticancer effects of AGG against human hepatocellular carcinoma in vitro and in vivo.
Cell proliferation, DNA fragmentation, Annexin V binding, immunocytofluorescence, Western blotting, caspase activity assays and luciferase assays were performed to evaluate AGG in human liver cancer cells HepG2. Immunohistochemical staining and TUNEL expression were studied in tumor samples of HepG2-xenografted nude mice.
AGG induced apoptosis in HepG2 cells in a dose- and time-dependent manner. AGG-treated HepG2 cells demonstrated an increase in caspase 3/7, 8 and 9 activities and a sharp decrease in the Bcl-2/Bax ratio, indicating activation of a caspase cascade. Co-treatment of HepG2 cells with AGG and a caspase inhibitor or treatment of AGG in Bax knockout HepG2 cells decreased the caspase 3/7 activity in comparison to HepG2 cells exposed only to AGG. Moreover, AGG decreased the expression of Hsp90 and suppressed Akt phosphorylation and NF-κB expression in HepG2 cells. Finally, AGG treatment significantly reduced tumor growth in nude mice bearing HepG2 xenografts, increased TUNEL expression and decreased CD-31 and Ki-67 expression compared to levels observed in the untreated control mice bearing HepG2 cells.
AGG inhibits the growth and progression of HepG2 cells by inducing caspase-mediated cell death. The agglutinin could be an alternative natural remedy for the treatment of human hepatocellular carcinomas.
源自印度药用植物相思子种子的相思子凝集素(AGG)属于II类核糖体失活蛋白家族。在本研究中,我们调查了AGG在体外和体内对人肝癌细胞的抗癌作用。
进行细胞增殖、DNA片段化、膜联蛋白V结合、免疫细胞荧光、蛋白质印迹、半胱天冬酶活性测定和荧光素酶测定,以评估AGG对人肝癌细胞HepG2的作用。在HepG2异种移植裸鼠的肿瘤样本中研究免疫组织化学染色和TUNEL表达。
AGG以剂量和时间依赖性方式诱导HepG2细胞凋亡。经AGG处理的HepG2细胞显示半胱天冬酶3/7、8和9活性增加,Bcl-2/Bax比值急剧下降,表明半胱天冬酶级联反应被激活。与仅暴露于AGG的HepG2细胞相比,用AGG和半胱天冬酶抑制剂共同处理HepG2细胞或在Bax基因敲除的HepG2细胞中用AGG处理可降低半胱天冬酶3/7活性。此外,AGG降低了HepG2细胞中Hsp90的表达,抑制了Akt磷酸化和NF-κB表达。最后,与未处理的携带HepG2细胞的对照小鼠相比,AGG处理显著降低了携带HepG2异种移植物的裸鼠的肿瘤生长,增加了TUNEL表达,降低了CD-31和Ki-67表达。
AGG通过诱导半胱天冬酶介导的细胞死亡来抑制HepG2细胞的生长和进展。该凝集素可能是治疗人类肝细胞癌的一种替代性天然药物。