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羧甲基化葡聚糖三甲基壳聚糖纳米粒共递送 STAT3 siRNA 和 BV6 抑制癌细胞进展。

Codelivery of STAT3 siRNA and BV6 by carboxymethyl dextran trimethyl chitosan nanoparticles suppresses cancer cell progression.

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Int J Pharm. 2020 May 15;581:119236. doi: 10.1016/j.ijpharm.2020.119236. Epub 2020 Mar 30.

Abstract

High expression of inhibitor of apoptosis (IAP) molecules in cancer cells promotes cancer cell chemoresistance. Use of BV6, a well-known IAP inhibitor, along with inhibition of signal transducer and activator of transcription 3 (STAT3), which is an important factor in the survival of tumor cells, and NIK as a mediator of BV6 unpredicted side effects, can induce effective apoptosis in tumor cells. The present study has investigated the combination therapy of cancer cells using Carboxymethyl Dextran-conjugated trimethyl chitosan (TMC-CMD) nanoparticles (NPs) loaded with NIK/STAT3-specific siRNA and BV6 to synergistically induce apoptosis in the breast, colorectal and melanoma cancer cell lines. Our results showed that in addition to enhanced pro-apoptotic effects, this combination therapy reduced proliferation, cell migration, colony formation, and angiogenesis, along with expression of factors including IL-10 and HIF in tumor cells. The results indicate the potential of this combination therapy for further investigation in animal models of cancer.

摘要

凋亡抑制因子(IAP)分子在癌细胞中的高表达促进了癌细胞的化疗耐药性。使用 BV6(一种已知的 IAP 抑制剂),结合抑制信号转导和转录激活因子 3(STAT3),这是肿瘤细胞存活的重要因素,以及 NIK 作为 BV6 意外副作用的介导物,可以诱导肿瘤细胞发生有效的细胞凋亡。本研究探讨了使用羧甲基葡聚糖偶联三甲基壳聚糖(TMC-CMD)纳米颗粒(NPs)负载 NIK/STAT3 特异性 siRNA 和 BV6 的联合治疗对乳腺癌、结直肠癌和黑色素瘤癌细胞系的协同诱导细胞凋亡的作用。我们的结果表明,除了增强促凋亡作用外,这种联合治疗还降低了肿瘤细胞的增殖、细胞迁移、集落形成和血管生成,同时还降低了包括 IL-10 和 HIF 在内的多种因子的表达。这些结果表明,这种联合治疗具有在癌症动物模型中进一步研究的潜力。

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