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1’-Acetoxychavicol acetate inhibits growth of human oral carcinoma xenograft in mice and potentiates cisplatin effect via proinflammatory microenvironment alterations

机译:1’-乙酰氧基查韦醇乙酸盐通过促炎性微环境改变抑制小鼠口腔癌异种移植物的生长并增强顺铂作用

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Background Oral cancers although preventable, possess a low five-year survival rate which has remained unchanged over the past three decades. In an attempt to find a more safe, affordable and effective treatment option, we describe here the use of 1’S-1’-acetoxychavicol acetate (ACA), a component of Malaysian ginger traditionally used for various medicinal purposes. Methods Whether ACA can inhibit the growth of oral squamous cell carcinoma (SCC) cells alone or in combination with cisplatin (CDDP), was explored both in vitro using MTT assays and in vivo using Nu/Nu mice. Occurrence of apoptosis was assessed using PARP and DNA fragmentation assays, while the mode of action were elucidated through global expression profiling followed by Western blotting and IHC assays. Results We found that ACA alone inhibited the growth of oral SCC cells, induced apoptosis and suppressed its migration rate, while minimally affecting HMEC normal cells. ACA further enhanced the cytotoxic effects of CDDP in a synergistic manner as suggested by combination index studies. We also found that ACA inhibited the constitutive activation of NF-κB through suppression of IKKα/β activation. Human oral tumor xenografts studies in mice revealed that ACA alone was as effective as CDDP in reducing tumor volume, and further potentiated CDDP effects when used in combination with minimal body weight loss. The effects of ACA also correlated with a down-regulation of NF-κB regulated gene (FasL and Bim), including proinflammatory (NF-κB and COX-2) and proliferative (cyclin D1) biomarkers in tumor tissue. Conclusion Overall, our results suggest that ACA inhibits the growth of oral SCC and further potentiates the effect of standard CDDP treatment by modulation of proinflammatory microenvironment. The current preclinical data could form the basis for further clinical trials to improve the current standards for oral cancer care using this active component from the Malaysian ginger.
机译:背景口腔癌虽然可以预防,但五年生存率很低,在过去的三十年中一直保持不变。为了找到一种更安全,负担得起且有效的治疗方法,我们在此介绍1'S-1'-乙酰氧基chavicol醋酸盐(ACA)的使用,这是传统上用于各种医疗目的的马来西亚生姜的一种成分。方法:使用MTT法体外和使用Nu / Nu小鼠体内研究ACA是单独抑制口腔鳞状细胞癌(SCC)细胞还是与顺铂(CDDP)组合都可以抑制其生长。使用PARP和DNA片段化分析评估凋亡的发生,同时通过整体表达谱分析,Western印迹和IHC分析来阐明其作用方式。结果我们发现,单独的ACA抑制口腔SCC细胞的生长,诱导凋亡并抑制其迁移速率,同时对HMEC正常细胞的影响最小。如组合指数研究所表明的,ACA以协同方式进一步增强了CDDP的细胞毒性作用。我们还发现,ACA通过抑制IKKα/β激活来抑制NF-κB的组成性激活。在小鼠中进行的人类口腔肿瘤异种移植研究表明,单独的ACA在减少肿瘤体积方面与CDDP一样有效,并且与最小的体重减轻组合使用时,进一步增强了CDDP的作用。 ACA的作用还与NF-κB调控基因(FasL和Bim)的下调相关,包括肿瘤组织中的促炎性(NF-κB和COX-2)和增殖性(cyclin D1)生物标志物。结论总体而言,我们的结果表明ACA通过调节促炎性微环境来抑制口腔SCC的生长并进一步增强标准CDDP治疗的效果。当前的临床前数据可以为进一步的临床试验奠定基础,以使用马来西亚姜汁中的这种活性成分改善口腔癌护理的当前标准。

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