杨文华, 杨向东, 史哲新, 高 宏, 汤 毅, 于文俊①, 吕俊秀①, 郝 征①. 蝎毒多肽提取物对白血病小鼠Bcl-2 SDF-1α与TGF-β1 表达的影响*[J]. 中国肿瘤临床, 2010, 37(8): 429-432. DOI: 10.3969/j.issn.1000-8179.2010.08.003
引用本文: 杨文华, 杨向东, 史哲新, 高 宏, 汤 毅, 于文俊①, 吕俊秀①, 郝 征①. 蝎毒多肽提取物对白血病小鼠Bcl-2 SDF-1α与TGF-β1 表达的影响*[J]. 中国肿瘤临床, 2010, 37(8): 429-432. DOI: 10.3969/j.issn.1000-8179.2010.08.003
YANG Wenhua1, YANG Xiangdong1, SHI Zhexin1, GAO Hong1, TANG Yi1, YU Wenjun2, LV Junxiu2, HAO Zheng2. The Effect of PESV on Bcl- 2, SDF- 1α and TGF-β1 Expression in Leukemia in Mice[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(8): 429-432. DOI: 10.3969/j.issn.1000-8179.2010.08.003
Citation: YANG Wenhua1, YANG Xiangdong1, SHI Zhexin1, GAO Hong1, TANG Yi1, YU Wenjun2, LV Junxiu2, HAO Zheng2. The Effect of PESV on Bcl- 2, SDF- 1α and TGF-β1 Expression in Leukemia in Mice[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(8): 429-432. DOI: 10.3969/j.issn.1000-8179.2010.08.003

蝎毒多肽提取物对白血病小鼠Bcl-2 SDF-1α与TGF-β1 表达的影响*

The Effect of PESV on Bcl- 2, SDF- 1α and TGF-β1 Expression in Leukemia in Mice

  • 摘要: 目的:探讨蝎毒多肽提取物(PESV)对白血病小鼠Bcl- 2、SDF-1 α 与TGF-β 1 表达的影响,探究PESV对白血病细胞增殖和浸润的影响与机制。方法:NOD-SCID 小鼠60只,按本课题前期研究方法,建立人白血病NOD-SCID 小鼠髓外浸润模型。选取造模成功的小鼠40只,随机分为4 组,每组10只,分别为高、中、低剂量组和模型组,另设同周龄正常NOD-SCID 小鼠10只为空白对照组。高、中、低剂量组每只分别尾静脉注射PESV 1.2mg/(kg ·d)、0.6mg/(kg ·d)、0.3mg/(kg ·d),模型组和空白组每只均尾静脉注射0.9% 的生理盐水0.3mL/d,35d 后全部处死,取血清和骨髓细胞培养液上清,用ELISA 法进行Bcl- 2、SDF-1 α 与TGF-β 1 的检测。结果:高、中、低剂量组存活率均高于模型组,高、中、低剂量组小鼠血清以及骨髓的Bcl- 2、SDF-1 α 均明显低于模型组(P<0.05),而TGF-β 1 均高于模型组,均以高剂量组效果最为明显(P<0.05)。 结论:蝎毒多肽提取物可以有效的降低白血病小鼠血清及骨髓中Bcl- 2、SDF-1α的表达,提高TGF-β1 的表达,具有较好的阻抑白血病细胞增殖和浸润的作用。

     

    Abstract: Objective:To investigate the effect of PESV on the expression of Bcl-2, SDF- 1 α and TGF-β 1 and the multi -plication and infiltration of leukemic cells in leukemia in mice. Methods:A total of60NOD-SCID mice were used for model establishment of human leukemia with extra-marrow infiltration. Fourty successful models were randomly divided into 4 groups, with 10in each group (high-dose group, medium-dose group, low-dose group and model group). Another 10nor-mal NOD-SCID mice of the same age were used as the blank control group. In high-, medium- and low-dose groups, the mice were injected through tail vein with PESV at1.2 mg/kg·d, 0.6 mg/ kg·d, 0.3 mg/kg·d, respectively. Mice in the model group and the blank control group received treatment of 0.9% physiological saline at0.3 mL/d. The mice were sacrificed at 35days after treatment. Elisa was used to detect Bcl-2, SDF- 1 α and TGF-β 1 in cell culture supernatant of serum and bone marrow. Results: The survival of mice in high-, medium- and low-dose groups was higher than that in the model group. Bcl- 2 and SDF-1 α expression in serum and bone marrow of the mice in high-, medium- and low-dose groups was signi fi -cantly lower than that in model group ( P<0.05). TGF-β 1 expression was higher in serum and bone marrow of the mice in high-, medium- and low-dose groups than in model group ( P<0.05). Conclusion:PESV can effectively reduce the expres-sion of Bcl- 2 and SDF-1 α in serum and bone marrow of mice wi th leukemia and enhance TGF-β 1 expression, and thus has inhibitory effect on multiplication and infiltration of leukemia cells.

     

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