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金属氧化物和量子点处理的HeLa细胞中凋亡途径蛋白表达的差异

Apoptotic pathway protein expression variance in metal oxide and quantum dot treated HeLa cells.

作者信息

Harris Seth, Kim Kyoungtae

机构信息

Biology, Missouri State University, Springfield, Missouri, United States.

出版信息

MicroPubl Biol. 2023 Jul 18;2023. doi: 10.17912/micropub.biology.000801. eCollection 2023.

DOI:10.17912/micropub.biology.000801
PMID:37602282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10435268/
Abstract

Using the HeLa cell line as a cancerous model, apoptotic protein expression was assessed upon various nanoparticle treatments. Utilizing a known chemotherapeutic agent, cisplatin, as a positive control for induction of apoptosis, several metal oxides (ZnO and CuO) and quantum dots (CdSe/ZnS and InP/ZnS) were investigated for their ability to express apoptotic markers. ZnO, CuO, green CdSe/ZnS, and green InP/ZnS were treated for 24 hours at their IC50 value. Western blot techniques were used to measure protein expression of phosphorylated p53 (ser15), PUMA, and p21 which are involved in signal transduction of apoptosis. CuO, ZnO, and CdSe/ZnS demonstrated considerable p53 activation at 24 hrs compared to the non-treated control. At the IC50 value, CdSe/ZnS quantum dots were the quickest at activating p53 by phosphorylation at the Serine 15 residue. Together, our results provide new insight into the apoptotic mechanism behind these treatments and lead to improved treatments against cancer.

摘要

以HeLa细胞系作为癌模型,评估了各种纳米颗粒处理后凋亡蛋白的表达情况。利用已知的化疗药物顺铂作为诱导凋亡的阳性对照,研究了几种金属氧化物(氧化锌和氧化铜)和量子点(硒化镉/硫化锌和磷化铟/硫化锌)表达凋亡标志物的能力。氧化锌、氧化铜、绿色硒化镉/硫化锌和绿色磷化铟/硫化锌在其半数抑制浓度(IC50)值下处理24小时。采用蛋白质印迹技术检测参与凋亡信号转导的磷酸化p53(丝氨酸15)、p53上调凋亡调节因子(PUMA)和p21的蛋白表达。与未处理的对照相比,氧化铜、氧化锌和硒化镉/硫化锌在24小时时显示出相当程度的p53激活。在IC50值时,硒化镉/硫化锌量子点通过丝氨酸15残基的磷酸化激活p53的速度最快。总之,我们的结果为这些处理背后的凋亡机制提供了新的见解,并有助于改进抗癌治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073d/10435268/40e4fac2ba40/25789430-2023-micropub.biology.000801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073d/10435268/40e4fac2ba40/25789430-2023-micropub.biology.000801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073d/10435268/40e4fac2ba40/25789430-2023-micropub.biology.000801.jpg

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