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Functional graphene oxide as cancer-targeted drug delivery system to selectively induce oesophageal cancer cell apoptosis

机译:作为癌症靶向药物递送系统的功能性石墨烯氧化物选择性地诱导食管癌细胞凋亡

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Graphene oxides (GO) is a promising building material to fabricate desired drug delivery system due to its excellent physicochemical properties. In this study, an innovative nano-drug (Ori@GE11-GO) was constructed based on GE11 peptide functionalized GO for targeted delivery of oridonin to realize the specific recognition of tumour cells and enhance anticancer efficiency. GE11 surface modification onto GO significantly increased the cellular uptake of GO in EGFR overexpressed oesophageal cancer cells (KYSE-30 and EC109 cells) than that of normal cells, indicating the EGFR targeting effects of Ori@GE11-GO. The internalized Ori@GE11-GO could accumulate into lysosomes and significantly inhibit the viability of cancer cells. Moreover, Ori@GE11-GO could effectively induce KYSE-30 and EC109 cells cycle arrest, apoptosis, mitochondrial membrane potential (om) disruption through the activation of apoptotic signalling pathways and the inhibition of EGFR/Ras/Raf/MEK/ERK signalling pathway, showing potential use of Ori@GE11-GO for cancer treatment. Taken together, this study demonstrates a good strategy for the construction of bio-functionalized GO drug delivery nanosystem to improve the cancer targeting efficiency of anticancer medicines.
机译:石墨烯氧化物(GO)是由于其优异的物理化学性质而制造所需的药物递送系统的承诺材料。在这项研究中,基于GE11肽官能化的创新纳米药物(ORI @ GE11-GO)进行了官能化的靶向递送,以实现肿瘤细胞的具体识别,提高抗癌效率。 GE11表面改性到Go显着增加了EGFR过表达食管癌细胞(Kyse-30和EC109细胞)的蜂窝摄取,表明ORI @ GE11-GO的EGFR靶向效果。内化的ORI @ GE11-GO可以积聚到溶酶体中并显着抑制癌细胞的活力。此外,ORI @Ge11-Go可以有效地诱导Kyse-30和EC109细胞周期停滞,细胞凋亡,通过激活凋亡信号通路和EGFR / RAS / RAF / MEK / ERK信号通路的抑制,显示潜在使用ORI @ GE11-GO用于癌症治疗。这项研究占据了,本研究表明了对生物官能化的去药递送纳米系统建造的良好策略,以改善抗癌药物的癌症靶向效率。

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