Scutellaria Barbata D.Don Inhibits Colorectal Cancer Growth via Suppression of Multiple Signaling Pa

来源 :第十一次中国中西医结合实验医学学术研讨会 | 被引量 : 0次 | 上传用户:H07081820607
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  The pathogenic mechanisms underlying cancer development are complex and heterogeneous,involving multiple cellular signaling transduction pathways which usually function redundantly.In addition,crosstalk between these pathways generates a complicated and robust signaling network that is regulated by compensatory mechanisms.Given the complexity of cancer pathogenesis and progression,many of the currently used anti-tumor agents,which typically target a single intracellular pathway,might not always be effective on complex tumor systems.Moreover,long-term use of these agents often generates drug resistance and toxicity against normal cells.Therefore,the development of novel anti-cancer ehemotherapies is urgently needed.Seutellaria barbata D.Don (SB) is a medicinal herb that has long been used in China to treat various types of cancer.We previously reported that the ethanol extract of SB (EESB) is able to induce colon cancer cell apoptosis,inhibit cell proliferation and tumor angiogenesis via modulation of several pathways including Hedgehog,Akt and p53.To further elucidate the precise mechanisms of SBs anti-tumor activity,using a colorectal cancer (CRC) mouse xenografl model in the present study,we evaluated the therapeutic efficacy and molecular mechanisms of EESB against tumor growth.We found that EESB reduced tumor volume and tumor weight but had no effect on body weight gain in CRC mice,demonstrating that EESB could inhibit colon cancer growth in vivo without apparent adverse effect.In addition,EESB treatment could significantly suppress the activation of several CRC-related pathways including STAT3,Erk and p38 signalings in tumor tissues,and alter the expression of multiple critical target genes such as Bcl-2,Bax,Cyclin D1,CDK4 and p21.These molecular effects lead to the induction of cancer cell apoptosis and inhibition of cell proliferation.Our findings demonstrate that Scutellaria barbata D.Don possesses a broad range of anti-tumor activities due to its ability to affect multiple intracellular targets.
其他文献
大肠癌是最常见的恶性肿瘤之一,生物标记物是存在于血液、体液或组织中的分子或物质,能够反映出特殊的生理及病理状态.而以血液和粪便为基础的生物标志物本文对DNA甲基化生物标记物在大肠癌中的应用进行了详细分析,相关基因甲基化水平作为大肠癌患病危险评估、诊断、治疗反应观察及疾病转归、预后评价的生物标记将有着很乐观的应用前景,DNA甲基化生物标记物有望能在今后大肠癌的诊断中占据一席之地。
会议
背景由于右半结肠供应血管分支的变异极其常见,血管分支不恒定、肠系膜上静脉及属支血管壁菲薄以及肥胖等因素,腹腔镜下右半结肠D3根治术的技术难度大。方法 通过典型录像总结介绍腹腔镜往复式右半结肠D3淋巴结清扫术的关键步骤及优缺点。关键技巧:采用五孔法完成手术,主刀站于患者两腿间手术,上腹两孔分别牵拉横结肠中段系膜及回结肠血管。右半结肠的D3淋巴结清扫术分为6个步骤:①显露肠系膜上静脉及自下而上切开血管
目的:从湿热毒淤各方面研究痹肿消汤及拆方对胶原诱导型关节炎模型大鼠滑膜IL-1和TNF的影响,进一步探讨该药物的作用机制.方法:90只健康雌性SD大鼠随机分为正常组、模型组、痹肿消汤组(简称全方组)及清热解毒中药干预组(简称拆方1组)、祛湿中药干预组(简称拆方2组)、活血中药干预组(简称拆方3组).除正常组之外各组大鼠采用皮下注射牛II型胶原与完全弗氏佐剂建立胶原诱导型关节炎大鼠模型,观察痹肿消汤
目的:探讨中医清热活血方药抑制CIA大鼠骨破坏的机制.方法:试验分为正常对照组(A组)、模型对照组(B组)、MTX组(C组)和风湿清组(D组),除A组外,其余各组大鼠CIA造模,C组与D组免疫后第14d开始给药,给药直至第49d.以足肿胀、病理切片、骨密度及血清中IL-17、RANKL、MIP-1a的表达水平综合评价清热活血方药对CIA大鼠骨破坏的干预情况.结果:造模后足肿胀明显、足部关节骨破坏严
目的:探讨朱砂及其复方朱砂安神丸中汞对肝、肾组织病理及金属硫蛋白表达的影响,并与硫化汞、氯化汞,甲基汞做对比研究.方法:健康小鼠42只,随机分成7组,分别为正常组、HgS组、朱砂组、朱砂高剂量组、朱砂安神丸组、HgCl2组、甲基汞组,每组6只.分别灌胃给予等量生理盐水、HgS 0.2g·kg-1、朱砂0.2g·kg-1、高剂量朱砂2g·kg-1、朱砂安神丸1.8g·kg-1、HgCl20.032
目的:探讨山药多糖抗神经细胞缺氧性凋亡作用及机制.方法:研究分为正常对照组,凋亡诱导组,山药多糖0.025g/L组,山药多糖0.05g/L组,山药多糖0.1g/L组,山药多糖0.25g/L组.采用"Neurobasal+B27"体外神经细胞无血清培养,免疫细胞化学鉴定神经细胞,MTT测定药物毒性,Rh-123染色检测线粒体损伤,AnnexinV/PI双染流式细胞仪及Hochest33342荧光染色
Based on the pathophysiology of brain,advance in angiogenesis induced by stroke,and evidences of traditional-Chinese-medicine-mediated angiogenesis,the possibility to study the treating-stroke mechani
目的:观察人参三七川芎提取物对AngⅡ诱导的人脐静脉血管内皮细胞(HUVEC)衰老的干预作用及其时效性特征,以探讨益气活血中药抗血管疾病的作用特点.方法:体外培养HUVECs加入终浓度10-6mol/L Ang Ⅱ诱导细胞衰老,建立血管内皮细胞衰老模型.实验分为空白对照组、AngⅡ模型组、中药提取物组和替米沙坦组;采用β-半乳糖苷酶染色法鉴定内皮细胞的衰老状态,双抗体夹心酶标免疫分析法测定细胞培养
目的:探讨黄芪糖蛋白(HuangQi Glycoprotein,HQGP)对佐剂性关节炎(adjuvant arthritis,AA)大鼠外周免疫及滑膜凋亡的影响.方法:建立大鼠AA模型,一周后给药治疗,三周后取各组大鼠外周血及膝关节滑膜组织,采用流式细胞术检测大鼠外周血淋巴细胞亚群CD3+、CD25+、CD28+、CD278+的细胞比例和淋巴细胞凋亡水平,采用TUNEL检测大鼠膝关节滑膜的细胞凋