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重组人制瘤素蛋白在胰腺癌治疗中的作用

Effects of recombinant human canstatin protein in the treatment of pancreatic cancer.

作者信息

He Xiao-Ping, Li Zhao-Shen, Zhu Ren-Min, Tu Zhen-Xing, Gao Jun, Pan Xue, Gong Yan-Fang, Jin Jing, Man Xiao-Hua, Wu Hong-Yu, Xu Ai-Fang

机构信息

Department of Gastroenterology, Nanjing General Hospital, Jiangsu Province, and Second Military Medical University, Shanghai, China.

出版信息

World J Gastroenterol. 2006 Nov 7;12(41):6652-7. doi: 10.3748/wjg.v12.i41.6652.

Abstract

AIM

To examine the effect of canstatin, a newly discovered endogenous inhibitor of angiogenesis, in the treatment of pancreatic cancer in vivo.

METHODS

The canstatin cDNA fragment was synthesized and amplified from the total RNA extracted from human placenta tissues by RT-PCR. The resulting product was firstly cloned into pUCm-T vector, then into plasmid pET-22b (+) and transformed into E. coli BL21. Isopropyl-1-thio-b-Dgalactopyran-oside (IPTG) was used to induce the expression of canstatin protein and affinity chromatography was used to purify the protein. To determine the activity of purified recombinant human canstatin (rhCanstatin), orthotopic xenograft human pancreatic cancer models were established. Human pancreatic cancer cells (SW1990) were injected into the pancreas of BALB/c nude mice. Twenty-four nude mice with orthotopic xenograft tumor were randomly divided into 3 groups 10 d after the inoculation, and were treated with PBS 0.3 mL, or canstatin 5 mg/kg, or 10 mg/kg per day for 3 wk intraperitoneally. When the experiment was over, all tumors were resected and the effects of rhCanstatin on tumor growth, microvessel density (MVD) were analyzed.

RESULTS

After IPTG induction, SDS-PAGE showed a new monomeric 24 kDa protein band. This protein was purified through affinity chromatography and refolded through dialysis with a final concentration of 60 mg/L. In orthotopic pancreatic cancer models, the final tumor volume in groups treated with PBS, canstatin 5 mg/kg, 10 mg/kg were 355.21+/-39.54 mm3, 112.73+/-10.47 mm3, and 61.75+/-6.99 mm3 respectively. The immunohistochemical examination showed that the MVD in tumors treated with canstatin was significantly less than that in other group.

CONCLUSION

These findings demonstrate that the rhCanstatin effectively retards the growth of pancreatic cancer in a dose-dependent manner through inhibiting angiogenesis and may be a promising therapeutic agent for pancreatic cancer treatment in the clinic.

摘要

目的

研究新发现的血管生成内源性抑制剂制瘤素在体内治疗胰腺癌的效果。

方法

通过逆转录聚合酶链反应(RT-PCR)从人胎盘组织提取的总RNA中合成并扩增产制瘤素cDNA片段。所得产物首先克隆到pUCm-T载体中,然后克隆到质粒pET-22b(+)中,并转化到大肠杆菌BL21中。用异丙基-β-D-硫代半乳糖苷(IPTG)诱导制瘤素蛋白表达,并用亲和层析法纯化该蛋白。为确定纯化的重组人制瘤素(rhCanstatin)的活性,建立原位异种移植人胰腺癌模型。将人胰腺癌细胞(SW1990)注入BALB/c裸鼠的胰腺。接种后10天,将24只原位异种移植肿瘤裸鼠随机分为3组,分别腹腔注射0.3 mL PBS,或5 mg/kg制瘤素,或10 mg/kg制瘤素,每天1次,共3周。实验结束时,切除所有肿瘤,分析rhCanstatin对肿瘤生长、微血管密度(MVD)的影响。

结果

IPTG诱导后,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)显示一条新的24 kDa单体蛋白带。该蛋白通过亲和层析纯化,并通过透析复性,终浓度为60 mg/L。在原位胰腺癌模型中,用PBS、5 mg/kg制瘤素、10 mg/kg制瘤素治疗组的最终肿瘤体积分别为355.21±39.54 mm3、112.73±10.47 mm3和61.75±6.99 mm3。免疫组化检查显示,制瘤素治疗的肿瘤中MVD明显低于其他组。

结论

这些结果表明,rhCanstatin通过抑制血管生成以剂量依赖的方式有效延缓胰腺癌的生长,可能是临床上一种有前途的胰腺癌治疗药物。

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