Sinha Niharika, Panda Prashanta Kumar, Naik Prajna Paramita, Maiti Tapas K, Bhutia Sujit K
1 Department of Life science, National Institute of Technology Rourkela, Rourkela, India.
2 Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, India.
Tumour Biol. 2017 May;39(5):1010428317701634. doi: 10.1177/1010428317701634.
The accumulating evidences show that Abrus agglutinin, a plant lectin, displays a broad range of anticancer activity including cancer-specific induction of apoptosis; however, the underlying molecular mechanism of Abrus agglutinin-induced oral cancer stem cell elimination remains elusive. Our data documented that Abrus agglutinin effectively downregulated the CD44 expression with the increased CD44 population in different oral cancer cells. After 24-h Abrus agglutinin treatment, FaDu cells were quantified for orosphere formation in ultra-low attachment plates and data showed that Abrus agglutinin inhibited the number and size of orosphere in a dose-dependent manner in FaDu cells. Furthermore, Abrus agglutinin hindered the plasticity of FaDu orospheres as supported by reduced sphere formation and downregulated the self-renewal property via inhibition of Wnt-β-catenin signaling pathway. Introduction of LiCl, a glycogen synthase kinase 3β inhibitor, rescued the Abrus agglutinin-stimulated inhibition of β-catenin and phosphorylated glycogen synthase kinase 3β in FaDu cell-derived orospheres confirming importance of Wnt signaling in Abrus agglutinin-mediated inhibition of stemness. In this connection, our data showed that Abrus agglutinin restrained proliferation and induced apoptosis in FaDu-derived cancer stem cells in dose-dependent manner. Moreover, western blot data demonstrated that Abrus agglutinin increased the Bax/Bcl-2 ratio with activation of poly(adenosine diphosphate-ribose) polymerase and caspase-3 favoring apoptosis induction in orospheres. Abrus agglutinin induced reactive oxygen species accumulation in orospheres and pretreatment of N-acetyl cysteine, and a reactive oxygen species scavenger inhibited Abrus agglutinin-mediated caspase-3 activity and β-catenin expression indicating reactive oxygen species as a principal regulator of Wnt signaling and apoptosis. In conclusion, Abrus agglutinin has a potential role as an integrative therapeutic approach for combating oral cancer through targeting self-renewability of orospheres via reactive oxygen species-mediated apoptosis.
越来越多的证据表明,植物凝集素相思子凝集素具有广泛的抗癌活性,包括对癌症特异性的凋亡诱导作用;然而,相思子凝集素诱导口腔癌干细胞消除的潜在分子机制仍不清楚。我们的数据表明,相思子凝集素在不同的口腔癌细胞中能有效下调CD44的表达,同时增加CD44的表达量。用相思子凝集素处理24小时后,对超低附着板中FaDu细胞的成球能力进行定量分析,数据显示相思子凝集素以剂量依赖的方式抑制FaDu细胞中的球状体数量和大小。此外,相思子凝集素通过减少球状体形成阻碍了FaDu球状体的可塑性,并通过抑制Wnt-β-连环蛋白信号通路下调了自我更新特性。糖原合酶激酶3β抑制剂LiCl的引入挽救了相思子凝集素对FaDu细胞来源球状体中β-连环蛋白和磷酸化糖原合酶激酶3β的抑制作用,证实了Wnt信号在相思子凝集素介导的干性抑制中的重要性。在此方面,我们的数据表明,相思子凝集素以剂量依赖的方式抑制FaDu来源的癌症干细胞增殖并诱导其凋亡。此外,蛋白质印迹数据表明,相思子凝集素增加了Bax/Bcl-2的比值,激活了聚(腺苷二磷酸核糖)聚合酶和半胱天冬酶-3,有利于球状体中凋亡的诱导。相思子凝集素诱导球状体中活性氧的积累,N-乙酰半胱氨酸(一种活性氧清除剂)预处理可抑制相思子凝集素介导的半胱天冬酶-3活性和β-连环蛋白表达,表明活性氧是Wnt信号和凋亡的主要调节因子。总之,相思子凝集素通过活性氧介导的凋亡靶向球状体的自我更新能力,在对抗口腔癌方面具有作为综合治疗方法的潜在作用。