【摘 要】
:
Objective: The present study aimed to investigate the inhibitory effects of Gubenyiliu Formula II (GFII) and its blood activation prescriptions on the growth of MCF-7 human breast cancer xengrafts in
【出 处】
:
第五届国际中医、中西医结合肿瘤学术交流大会暨第十四届全国中西医结合肿瘤学术大会
论文部分内容阅读
Objective: The present study aimed to investigate the inhibitory effects of Gubenyiliu Formula II (GFII) and its blood activation prescriptions on the growth of MCF-7 human breast cancer xengrafts in nude mice,and explore their mechanisms of action.Methods: After the establishment of the MCF-7 human breast cancer xenograft model in nude mice,the mice in the GFII and its blood activation groups were administered with GFII (6.56 g/ml) and blood activation prescriptions (1.65 g/ml) by gavage for 28 days,respectively.The tumor volume and weight were measured twice a week throughout the treatment period.Apoptotic cells were identified by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling.The expression of microtubule associated protein 1 light chain 3 (LC3) was examined by immunohistochemistry,and western blotting analysis was performed to detect the expression of anti-apoptotic protein Bcl-2 andLC3 Meanwhile,the effects on PI3K/Akt/mTOR signaling pathway were also determined by western blotting analysis.Results: Compared with the control group,GFII group and its blood activation prescriptions could significantly inhibit the growth of MCF-7 human breast cancer xenografts in nude mice.The expression of Bcl-2 protein was lower in the GFII and blood activation groups than in the control group,whereas both the percentage of apoptotic cells and LC3-II/LC3-I ratio were higher than in the control group.In addition,a significantly reduced expression of phospho-Akt,phospho-mTOR and mTOR was observed in the blood activation group (P<0.05).Conclusions: To some extent,GFII and its blood activation prescriptions can exert their inhibitory effect on the growth of MCF-7 human breast cancer xenografts by inducing the cell apoptosis and autophagy.In addition to the induction of cell apoptosis,we also found that the blood activation prescriptions of GFII could induce cell autophagy by inhibiting of PI3K/AKT/mTOR signaling pathway,and then suppress the breast cancer cell growth.
其他文献
Background Aberrant hypermethylation of gene promoter regions is a primary mechanism by which tumor suppressor genes become inactivated in breast cancer.Epigenetic inactivation of the protein tyrosine
目的:晚期胰腺癌患者罕见长期生存,本文通过对胰腺癌长期带瘤生存患者分析,探索胰腺癌的最佳中西医结合治疗.方法:对复旦大学附属肿瘤医院在2002年1月至2007年12月六年期间收治病理确诊的生存超过3年胰腺癌患者进行回顾性研究.结果:20例生存超过3年晚期胰腺癌患者均带瘤生存(其中13例超过5年,最长生存169月),均采用中西医结合治疗.采用中医“清热化湿”为主治疗者疗效明显较优.结论:在晚期胰腺癌
Objectives: Pharmacologic treatment for cancer pain has some limitations; acupuncture may have a role in the management of cancer pain.More and more researches on acupuncture for cancer pain are emerg
目的:评价中西医综合治疗胰腺癌肝转移的疗效.方法:回顾性分析天津医科大学肿瘤医院2001~2010年间采用清热消积中药联合区域性动脉灌注和/或全身化疗治疗的292例胰腺癌肝转移患者的临床资料,随访其生存结果.依据治疗方案的不同,全部病例分为2组:西医治疗组(157例)、中西医治疗组(135例).西医治疗组均采用含吉西他滨(GEM)的化疗方案:GEM 1000 mg/m2,30分钟静滴,每周1次,连
Notch signaling plays a critical role for specifying the intestinalepithelial cell lineage and for initiating colorectal adenomas andcolorectal cancers (CRC).JAG2 as a ligand of Notch signaling pathwa
目的:探讨华蟾素对多发性骨髓瘤RPMI 8226细胞株增殖、凋亡的影响及作用机制.方法:分别采用四氮唑蓝(MTT)比色法、流式细胞仪检测华蟾素对多发性骨髓瘤RPMI 8226细胞增殖、凋亡的影响.用ELISA检测细胞上清液中白细胞介素-6(IL-6)及血管内皮生长因子(VEGF)水平.结果:1.不同浓度华蟾素对RPMI 8226 细胞的增殖均有抑制作用,随药物浓度的增加及作用时间的延长,药物的作用
目的:观察金福安汤对小鼠Lewis肺癌生长的抑制作用及其相关的分子机制.方法:将50只Lewis肺癌荷瘤小鼠分为金福安汤高、中、低剂量组,环磷酰胺(CTX)组,生理盐水组;计算各组小鼠平均瘤体质量、抑瘤率、肺表面转移灶及抗转移率;采用免疫组化法检测各组Lewis肺癌小鼠的p120ctn表达以及RhoA、Cdc42表达.结果:金福安汤各剂量组与CTX组的瘤体质量均小于生理盐水对照组的瘤体质量,其中中
目的:观察卡培他滨对人鼻咽癌细胞CNE-2的放射增敏作用,并探讨其可能的机制.方法:用MTT法测定卡培他滨抑制细胞增殖20%的药物浓度(IC20),以卡培他滨24h IC20浓度值对CNE-2细胞分别处理3h、6h、12h、24h,依次设为4 个卡培他滨+照射组,对其给予6MV X线分别单次照射0、2、4、6、8Gy,另设对照组为单纯照射组;用克隆形成实验计算各组的放射增敏比,得到细胞生存曲线;将
目的:鸦胆子油乳(Brucea Javanica oil emulsion,BJOE)是鸦胆子的石油醚提取物经磷脂乳化而成,在中国广泛用于肿瘤的辅助治疗.自噬是生物在进化上一种保守的自我保护机制,在抗肿瘤治疗过程中普遍被激活.大量的研究证实自噬在肿瘤的发生发展中发挥重要作用,但自噬在抗肿瘤治疗中的意义还未完全明了.本研究的目的在于探讨BJOE是否通过调控自噬来抑制HCT116 结肠癌细胞的增殖.方
目的:观察益气化瘀解毒方及方中单味药对人肝癌移植瘤及瘤组织MVD、HIF1a、VEGF及VEGFR-2、MMP-2、MMP-9、E-cad、Twist1、Bcl-2 等血管生成相关因子表达的影响.方法:建立人肝癌移植瘤模型,分为7组,分别以益气化瘀解毒方、单味药黄芪、莪术、重楼、壁虎、顺铂干预21后,取瘤组织行免疫组化检测.结果:(1)成瘤体积比较:给药后瘤体积及差值比较,各组与空白组比较有统计学