研究新型碳纳米管作为治疗剂在治疗三阴性乳腺癌 (TNBC) 中的作用--一项体外和体内研究。

Journal of cancer research updates Pub Date : 2024-01-01 Epub Date: 2024-11-11 DOI:10.30683/1929-2279.2024.13.06
Kamal Asadipour, Narendra Banerjee, Jazmine Cuffee, Karrington Perry, Shennel Brown, Anasua Banerjee, Erik Armstrong, Stephen Beebe, Hirendra Banerjee
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引用次数: 0

摘要

三阴性乳腺癌(TNBC)是全世界死亡率极高的恶性肿瘤。非裔美国人(AA)妇女死于三阴性乳腺癌(TNBC)的几率比诊断结果相同的白人妇女高出 28%。此外,非裔美国人患者更有可能被诊断为晚期乳腺癌,而且在任何诊断阶段的存活率都是最低的;现有的抗 TNBC 药物很少具有疗效,因此需要设计和研究更新的抗 TNBC 药物。近年来,碳纳米管(CNT)在各种癌症中显示出了有效的抗癌特性,这已在同行评审的期刊上有所报道。因此,我们对新型碳纳米管在 TNBC 体外和体内模型中的抗癌特性进行了研究。我们对 TNBC 模型 MDA-MB-231 VIM RFP 细胞系进行了体外细胞毒性研究,并对相同的癌细胞进行了球形体形成试验;我们还对 TNBC 模型小鼠进行了体内研究,以研究这种 CNT 药物在减少肿瘤负荷方面的疗效。我们的初步研究表明,与对照组相比,CNT 处理过的癌细胞的细胞死亡增加,球形细胞数量减少,TNBC 模型小鼠的肿瘤体积比未处理过的动物显著缩小。因此,我们的初步研究显示了新型 CNT 作为抗 TNBC 药物的显著疗效。在将这种新型纳米粒子作为治疗剂进行从实验室到临床的转化研究之前,还需要进行更多的机理研究,以找出细胞死亡机制、涉及的核心通路以及药代动力学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studying the Role of Novel Carbon Nano Tubes as a Therapeutic Agent to Treat Triple Negative Breast Cancer (TNBC) - an In Vitro and In Vivo Study.

Triple Negative Breast Cancer (TNBC) is a malignant cancer with a very high mortality rate around the world. African American(AA) women are 28% more likely to die from triple-negative breast cancer (TNBC) than white women with the same diagnosis. AA patients are also more likely to be diagnosed at a later stage of the disease and have the lowest survival rates for any stage of diagnosis; There are very few existing anti TNBC drugs with therapeutic efficacy hence newer anti TNBC drug design and investigation is needed. Carbon Nano Tubes(CNT) in recent years have shown effective anti-cancer properties in various types of cancers as reported in peer reviewed journals. Henceforth, we did an investigation to study the anticancer properties of a novel CNT in both in vitro and in vivo models of TNBC. We tested the CNT drug in vitro cytotoxicity studies on TNBC model MDA-MB-231 VIM RFP cell lines and Spheroid forming assays on the same cancer cells; we also did an in vivo study on TNBC model mice to study the therapeutic efficacy of this CNT drug in reducing the tumor load. Our initial studies showed increased cell death and reduction in spheroid numbers in the CNT treated cancer cells in comparison to control and a significant reduction in the tumor volume in the TNBC model mice than in untreated animals. Thus our initial studies have shown significant therapeutic efficacy of the novel CNT as an anti TNBC agent. Additional mechanistic studies need to be done to find out the cell death mechanisms, core canonical pathways involved, pharmacokinetic studies before translational research for this novel nanoparticle as a therapeutic agent from bench to bedside.

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