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Anti-Pancreatic Cancer Deliverables from Sea: First-Hand Evidence on the Efficacy Molecular Targets and Mode of Action for Multifarious Polyphenols from Five Different Brown-Algae

机译:来自海上的抗胰腺癌药物:来自五种不同褐藻的多种多酚的功效分子靶标和作用方式的第一手证据

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摘要

Pancreatic cancer (PC) remains the fourth leading cause of cancer death with an unacceptable survival that has remained relatively unchanged over the past 25 years. The presence of occult or clinical metastases at the time of diagnosis together with the lack of effective chemotherapies pose a dire need for designing new and targeted therapeutic deliverables that favors the clinical outcome. Herein, we investigated the anti-tumorigenic potential of polyphenols from five different brown-algae in human PC cells (MiaPaCa-2, Panc-1, BXPC-3 and Panc-3.27). Total anti-oxidant capacity (TAC) analysis on stepwise polyphenol separations with increasing polarity (Hexane-DCM-EA-methanol) identified high levels of TAC in DCM and EA extractions across all seaweeds assessed. All DCM and EA separated polyphenols induced a dose-dependent and sustained (time-independent) inhibition of cell proliferation and viability. Further, these polyphenols profoundly enhanced DNA damage (acridine orange/Ethidium bromide staining and DNA fragmentation) in all the cell lines investigated. More importantly, luciferase reporter assay revealed a significant inhibition of NFκB transcription in cells treated with polyphenols. Interestingly, QPCR analysis identified a differential yet definite regulation of pro-tumorigenic EGFR, VEGFA, AKT, hTERT, kRas, Bcl2, FGFα and PDGFα transcription in cells treated with DCM and EA polyphenols. Immunoblotting validates the inhibitory potential of seaweed polyphenols in EGFR phosphorylation, kRas, AurKβ and Stat3. Together, these data suggest that intermediate polarity based fractions of seaweed polyphenols may significantly potentiate tumor cell killing and may serve as potential drug deliverable for PC cure. More Studies dissecting out the active constituents in potent fractions, mechanisms of action and synergism, if any, are warranted and are currently in process.
机译:胰腺癌(PC)仍然是癌症死亡的第四大主要原因,其存活率令人无法接受,并且在过去25年中相对保持不变。诊断时隐匿或临床转移的存在以及缺乏有效的化学疗法,迫切需要设计出有利于临床结果的新型靶向治疗药物。在这里,我们调查了人类PC细胞(MiaPaCa-2,Panc-1,BXPC-3和Panc-3.27)中来自五个不同褐藻的多酚的抗致瘤潜力。随着极性的增加(己烷-DCM-EA-甲醇)逐步进行多酚分离,总抗氧化剂能力(TAC)分析表明,在所有评估的海藻中,DCM和EA提取物中的TAC含量较高。所有DCM和EA分离的多酚均诱导剂量依赖性和持续性(时间依赖性)抑制细胞增殖和活力。此外,这些多酚在所有研究的细胞系中均显着增强了DNA损伤(ac啶橙/溴乙锭染色和DNA片段化)。更重要的是,萤光素酶报告基因检测结果显示,用多酚处理的细胞对NFκB转录有明显的抑制作用。有趣的是,QPCR分析鉴定了用DCM和EA多酚处理的细胞中促肿瘤原性EGFR,VEGFA,AKT,hTERT,kRas,Bcl2,FGFα和PDGFα转录的差异但明确的调节。免疫印迹验证了海藻多酚对EGFR磷酸化,kRas,AurKβ和Stat3的抑制潜力。总之,这些数据表明,基于海藻多酚的中间极性级分可能会显着增强肿瘤细胞的杀伤力,并可能作为可用于PC治愈的潜在药物。需要对有效成分的有效成分,作用机理和协同作用(如果有)进行剖析的更多研究正在进行中。

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