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首页> 外文期刊>Nutrition and Cancer: An International Journal >Synergistic Antiproliferative Effects of Co-nanoencapsulated Curcumin and Chrysin on MDA-MB-231 Breast Cancer Cells Through Upregulating miR-132 and miR-502c
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Synergistic Antiproliferative Effects of Co-nanoencapsulated Curcumin and Chrysin on MDA-MB-231 Breast Cancer Cells Through Upregulating miR-132 and miR-502c

机译:通过上调miR-132和miR-502c通过上调MIR-132和miR-502c对MDA-MB-231乳腺癌细胞进行协同抗增殖效果

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In this study, we explored whether co-nanoencapsulated Curcumin (Cur) and Chrysin (Chr), natural herbal compounds with antitumor activities, regulate miR-132 and miR-502c and their downstream targets, leading to the synergistic growth inhibition in MDA-MB-231 breast cancer cells. For this purpose, Cur and Chr were co-encapsulated into PLGA-PEG nanoparticles (NPs) and characterized through DLS, FTIR and FE-SEM. MTT assay and cell cycle arrest analysis revealed that CurChr-loaded NPs had a considerable synergistic cytotoxicity against MDA-MB-231 cells with more cell accumulation in G2/M phase compared to the other groups. In addition, highest percentage of cell apoptosis was acquired in cells treated with CurChr-loaded NPs according to apoptosis analysis. Real-time PCR findings revealed that co-encapsulated form of Cur and Chr than free combination could further upregulate miR-132 and miR-502c expression (P?
机译:在该研究中,我们探讨了与抗肿瘤活性的共纳淀粉(CHR)和Chrysin(CHR),天然草药化合物,调节miR-132和miR-502c及其下游靶标,导致MDA-MB中的协同生长抑制-231乳腺癌细胞。为此目的,Cur和Chr被共涂在PLGA-PEG纳米颗粒(NPS)中,并通过DLS,FTIR和Fe-SEM表征。 MTT测定和细胞周期停滞分析显示,与其他基团相比,Curchr加载的NPS对MDA-MB-231细胞具有相当大的协同细胞毒性,其G2 / M相中具有更多细胞积累。此外,根据细胞凋亡分析,在用Curchr负载的NPS处理的细胞中获得最高百分比的细胞凋亡。实时PCR发现显示,与游离组合的Cur和Chr的共同包封形式可以进一步上调miR-132和miR-502c表达(p?<0.001)。此外,在用CRC和CHR中的细胞中,在细胞的HN1和P65的蛋白质​​水平中检测到强的还原。这些发现表明,通过靶向miR-132和miR-205c的Cur和Chr的共纳纳频可能是治疗乳腺癌的新策略。

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