检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘春花[1,2] 隋文文[1,3] 王兆朋[1] 张月英[1] 张维东[1]
机构地区:[1]山东省医学科学院基础医学研究所病理室,山东济南250062 [2]青岛市胶州中心医院产科,山东青岛266300 [3]济南市第二人民医院病理科,山东济南250062
出 处:《中草药》2015年第7期1018-1022,共5页Chinese Traditional and Herbal Drugs
基 金:国家自然科学基金资助项目(81073102;30873408)
摘 要:目的研究蝎毒多肽抑制卵巢癌裸鼠肿瘤生长的作用机制,为恶性肿瘤临床治疗提供理论依据。方法制备人SKOV3裸鼠异种移植瘤模型,蝎毒多肽高、低剂量(20、10 mg/kg)ig给药2周,绘制肿瘤体积增长曲线,并计算抑瘤率;HE染色法观察各组肿瘤组织病理变化;免疫组化法检测肿瘤组织中PTEN、PI3K、p-Akt的表达水平;ELISA法检测各组裸鼠血清中PTEN、PI3K、p-Akt水平。结果蝎毒多肽高、低剂量组的抑瘤率分别为50.8%和31.5%。与对照组相比,蝎毒多肽高、低剂量组裸鼠肿瘤组织中PI3K和p-Akt的表达明显下调(P<0.05、0.01),PTEN的表达明显上调(P<0.05、0.01);血清中各因子的变化与免疫组化结果一致。结论蝎毒多肽可抑制卵巢癌肿瘤的生长,其机制可能与抑制肿瘤微环境中PI3K、p-Akt的表达,上调PTEN的表达有关。Objective To research the inhibitory mechanism of the polypeptide extract from scorpion venom(polypeptide extract from scorpion venom, PESV) on tumor growth, which would provides the theory basis for clinic treatment of malignant tumor. Methods SKOV3 xenograft models were established, and tumors were excised after administration to observe the inhibitory effect of PESV. The effect of PESV on the tumor growth was observed by recording tumor growth curve and calculating the inhibitory rate; Immunohistochemistry and ELISA were applied to detect the levels of PTEN, PI3 K, and P-Akt. Results The inhibitory rates of the high-dose(20 mg/kg) and low-dose(10 mg/kg) PESV groups were 50.8% and 31.5%. Compared with the control group, the protein expressions of PI3 K and P-Akt significantly decreased(P〈0.05 or 0.01) and the protein expressions of PTEN significantly increased(P〈0.05 or 0.01) in the high-and low-dose PESV groups. Conclusion PESV could inhibit the growth of ovarian cancer. Its mechanisms might be associated with inhibiting the expressions of PI3 K and P-Akt and increasing PTEN in the microenvironment of tumors.
关 键 词:蝎毒多肽 PI3K/AKT信号转导通路 卵巢癌 PTEN 肿瘤微环境
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.249