首页> 外文期刊>International journal of oncology >Anticarcinogenic effects of water extract of sporoderm-broken spores of Ganoderma lucidum on colorectal cancer in vitro and in vivo
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Anticarcinogenic effects of water extract of sporoderm-broken spores of Ganoderma lucidum on colorectal cancer in vitro and in vivo

机译:灵芝孢子体破壁孢子水提取物对大肠癌的体内外抗癌作用

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Ganoderma lucidum (G.?lucidum) polysaccharides (GLPs) have been used as traditional Chinese medicine for cancer prevention for many years. However, the mechanism by which GLP exerts its chemopreventive activities remains elusive. In addition, it is unclear whether sporoderm-broken spores of G.?lucidum water extract (BSGLWE), which contains mainly GLPs, has anticancer effects on colorectal cancer. The present study investigated the anticancer effects and potential mechanisms of BSGLWE on colorectal cancer in?vivo and in?vitro. Our results showed that BSGLWE significantly inhibited colorectal cancer HCT116 cell viability in a time- and dose-dependent manner. Flow cytometry analysis indicated that BSGLWE disrupted cell cycle progression at G2/M?phase via downregulation of cyclin?B1 and cyclin?A2, and upregulation of P21 at mRNA levels. Moreover, BSGLWE induced apoptosis by decreasing Bcl-2 and survivin at mRNA levels, and reduced Bcl-2, PARP, pro-caspase-3 and pro-caspase-9 at protein levels. Furthermore, BSGLWE suppressed tumor growth in?vivo by regulating the expression of genes and proteins associated with cell cycle and apoptosis, which was further confirmed by a reduction of Ki67, PCNA, and Bcl-2 expression as determined by immunohistochemistry staining. NSAID activated gene-1 (NAG-1), a pro-apoptotic gene, was significantly upregulated in?vivo and in?vitro upon BSGLWE treatment at both mRNA and protein levels. In addition, the relative amounts of secreted NAG-1 in cell culture medium or serum of nude mice were all upregulated upon BSGLWE treatments, suggesting a role of NAG-1 in BSGLWE-induced anticolorectal cancer activity. This is the first study to show that BSGLWE inhibits colorectal cancer carcinogenesis through regulating genes responsible for cell proliferation, cell cycle and apoptosis cascades. These findings indicate that BSGLWE possesses chemopreventive potential in colorectal cancer which may serve as a promising anticancer agent for clinical applications.
机译:灵芝(G.lucidum)多糖(GLPs)已被用作预防癌症的传统中药多年。但是,GLP发挥其化学预防活性的机制仍然难以捉摸。此外,尚不清楚主要含有GLP的灵芝水提取物(BSGLWE)的孢子体破壁孢子是否对结肠直肠癌具有抗癌作用。本研究调查了BSGLWE对大肠癌在体内和体外的抗癌作用及其潜在机制。我们的结果表明,BSGLWE以时间和剂量依赖性方式显着抑制结肠直肠癌HCT116细胞的活力。流式细胞仪分析表明,BSGLWE通过下调细胞周期蛋白B1和细胞周期蛋白A2以及上调P21在mRNA水平上破坏了G2 / M2期的细胞周期进程。此外,BSGLWE通过在mRNA水平上降低Bcl-2和survivin诱导凋亡,并在蛋白水平上降低Bcl-2,PARP,caspase-3和caspase-9。此外,BSGLWE通过调节与细胞周期和细胞凋亡相关的基因和蛋白质的表达来抑制肿瘤的体内生长,这通过免疫组织化学染色确定的Ki67,PCNA和Bcl-2表达的降低进一步得到证实。 BSGLWE处理后,NSAID激活基因-1(NAG-1)是一种促凋亡基因,在mRNA和蛋白质水平上均在体内和体外显着上调。此外,BSGLWE处理后,裸鼠的细胞培养基或裸鼠血清中分泌的NAG-1的相对量均被上调,表明NAG-1在BSGLWE诱导的抗结直肠癌活性中的作用。这是第一项表明BSGLWE通过调节负责细胞增殖,细胞周期和细胞凋亡级联的基因来抑制结肠直肠癌致癌作用的研究。这些发现表明,BSGLWE在结直肠癌中具有化学预防的潜力,可作为临床应用中有希望的抗癌药。

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