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介孔石墨烯和氧化石墨烯与蜂毒素复合物对鸡胚尿囊膜上生长的三阴性乳腺癌肿瘤的影响。

Effect of Melittin Complexes with Graphene and Graphene Oxide on Triple-Negative Breast Cancer Tumors Grown on Chicken Embryo Chorioallantoic Membrane.

机构信息

Department of Nanobiotechnology, Institute of Biology, Warsaw University of Life Sciences, 02-786 Warsaw, Poland.

出版信息

Int J Mol Sci. 2023 May 7;24(9):8388. doi: 10.3390/ijms24098388.

Abstract

One of the components of bee venom is melittin (M), which has strong lysing properties on membranes. M has high toxicity to cancer cells, but it also affects healthy cells, making it necessary to use methods for targeted delivery to ensure treatment. This research is a continuation of previous studies using graphene nanomaterials as M carriers to breast cancer cells. The studies described below are conducted on a more organized biological structure than what is found in vitro cells, namely, cancerous tumors grown on a chicken embryo chorioallantoic membrane. Caspase 3 and 8 levels are analyzed, and the level of oxidative stress markers and changes in protein expression for cytokines are examined. The results show that M complexes with nanomaterials reduce the level of oxidative stress more than M alone does, but the use of graphene (GN) as a carrier increases the level of DNA damage to a greater extent than the increase caused by M alone. An analysis of cytokine levels shows that the use of the M and GN complex increases the level of proteins responsible for inhibiting tumor progression to a greater extent than the increase occasioned by a complex with graphene oxide (GO). The results suggest that the use of GN as an M carrier may increase the toxic effect of M on structures located inside a cell.

摘要

蜂毒的一种成分是蜂毒素 (M),它对细胞膜具有很强的裂解性质。M 对癌细胞有很高的毒性,但也会影响健康细胞,因此需要使用靶向递送来确保治疗效果。本研究是使用石墨烯纳米材料作为 M 载体递送到乳腺癌细胞的先前研究的延续。下面描述的研究是在比体外细胞更有组织的生物结构上进行的,即在鸡胚绒毛尿囊膜上生长的癌性肿瘤。分析了半胱天冬酶 3 和 8 的水平,并检查了氧化应激标志物的水平和细胞因子的蛋白质表达变化。结果表明,M 与纳米材料的复合物降低了氧化应激水平,比单独的 M 降低得更多,但与单独使用 M 相比,石墨烯 (GN) 作为载体的使用会更大程度地增加 DNA 损伤水平。细胞因子水平的分析表明,与氧化石墨烯 (GO) 复合物相比,使用 M 和 GN 复合物会更大程度地增加负责抑制肿瘤进展的蛋白质水平。结果表明,使用 GN 作为 M 载体可能会增加 M 对细胞内结构的毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b8/10179033/1177593475d9/ijms-24-08388-g001.jpg

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