临床肿瘤学杂志
臨床腫瘤學雜誌
림상종류학잡지
CHINESE CLINICAL ONCOLOGY
2014年
10期
876-880
,共5页
陆萌%吴苏稼%施鑫%周光新%黎承军%赵建宁
陸萌%吳囌稼%施鑫%週光新%黎承軍%趙建寧
륙맹%오소가%시흠%주광신%려승군%조건저
贝伐单抗%骨肉瘤%生长%血管再生
貝伐單抗%骨肉瘤%生長%血管再生
패벌단항%골육류%생장%혈관재생
Bvacizumab%Osteosarcoma%Growth%Angiogenesis
目的:探讨贝伐单抗( Avastin)对人骨肉瘤143-B裸鼠移植瘤模型生长和血管生成的影响。方法将成功建立的红色荧光蛋白标记的人骨肉瘤143-B 裸鼠原位种植模型随机分为3组:对照组(生理盐水)、低剂量贝伐单抗组( Avastin-L,2.0mg/kg)和高剂量贝伐单抗组( Avastin-H,5.0mg/kg),每组7只。贝伐单抗每次腹腔注射0.2ml,1周2次,持续3周;对照组给予等体积生理盐水。每隔3天记录各组体质量,每隔7天用荧光影像系统测量原位肿瘤大小并计算抑瘤率;采用免疫组化En Vision法检测各组肿瘤组织中的CD34表达并计算微血管密度( MVD);酶联免疫吸附法检测各组血浆和肿瘤组织的血管内皮生长因子( VEGF)的水平。结果3组实验裸鼠体质量及肺部转移率的差异无统计学意义( P>0.05);与对照组相比,Avastin-L组和Avastin-H组的肿瘤体积减小, MVD、血浆及肿瘤组织的 VEGF水平降低,差异均有统计学意义( P<0.05);Avastin-H组对上述指标的改善程度优于Avastin-L组( P<0.05)。结论 Avastin对人骨肉瘤143-B肿瘤生长有抑制作用,同时可降低血管生成及VEGF水平,但对肺部转移无明显抑制作用。
目的:探討貝伐單抗( Avastin)對人骨肉瘤143-B裸鼠移植瘤模型生長和血管生成的影響。方法將成功建立的紅色熒光蛋白標記的人骨肉瘤143-B 裸鼠原位種植模型隨機分為3組:對照組(生理鹽水)、低劑量貝伐單抗組( Avastin-L,2.0mg/kg)和高劑量貝伐單抗組( Avastin-H,5.0mg/kg),每組7隻。貝伐單抗每次腹腔註射0.2ml,1週2次,持續3週;對照組給予等體積生理鹽水。每隔3天記錄各組體質量,每隔7天用熒光影像繫統測量原位腫瘤大小併計算抑瘤率;採用免疫組化En Vision法檢測各組腫瘤組織中的CD34錶達併計算微血管密度( MVD);酶聯免疫吸附法檢測各組血漿和腫瘤組織的血管內皮生長因子( VEGF)的水平。結果3組實驗裸鼠體質量及肺部轉移率的差異無統計學意義( P>0.05);與對照組相比,Avastin-L組和Avastin-H組的腫瘤體積減小, MVD、血漿及腫瘤組織的 VEGF水平降低,差異均有統計學意義( P<0.05);Avastin-H組對上述指標的改善程度優于Avastin-L組( P<0.05)。結論 Avastin對人骨肉瘤143-B腫瘤生長有抑製作用,同時可降低血管生成及VEGF水平,但對肺部轉移無明顯抑製作用。
목적:탐토패벌단항( Avastin)대인골육류143-B라서이식류모형생장화혈관생성적영향。방법장성공건립적홍색형광단백표기적인골육류143-B 라서원위충식모형수궤분위3조:대조조(생리염수)、저제량패벌단항조( Avastin-L,2.0mg/kg)화고제량패벌단항조( Avastin-H,5.0mg/kg),매조7지。패벌단항매차복강주사0.2ml,1주2차,지속3주;대조조급여등체적생리염수。매격3천기록각조체질량,매격7천용형광영상계통측량원위종류대소병계산억류솔;채용면역조화En Vision법검측각조종류조직중적CD34표체병계산미혈관밀도( MVD);매련면역흡부법검측각조혈장화종류조직적혈관내피생장인자( VEGF)적수평。결과3조실험라서체질량급폐부전이솔적차이무통계학의의( P>0.05);여대조조상비,Avastin-L조화Avastin-H조적종류체적감소, MVD、혈장급종류조직적 VEGF수평강저,차이균유통계학의의( P<0.05);Avastin-H조대상술지표적개선정도우우Avastin-L조( P<0.05)。결론 Avastin대인골육류143-B종류생장유억제작용,동시가강저혈관생성급VEGF수평,단대폐부전이무명현억제작용。
Objective To explore the influence of bevacizumab ( Avastin) on the growth and angiogenesis of RFP-tagged os-teosarcoma orthotopic nude mice model of human osteosarcoma. Methods Twenty-one nude mice inoculated with human osteosarcoma cell line 143-B-RFP were randomly divided into three groups:control group, low dose Avastin group ( Avastin-L) and high dose Avas-tin group ( Avastin-H) . Avastin-L group and Avastin-H group received continuous 0. 2ml injection of 2. 0mg/kg or 5. 0mg/kg Avastin twice a week for 3 weeks, while control group was given an equal volume of saline. The body weight was recorded every 3 days. The in situ tumor size was measured to calculate the volume and the tumor inhibition rate every 7 days by fluorescence imaging system. Immu-nohistochemical En Vision method was used to detect the expression of CD34 in tumor tissue to evaluate the microvessel density ( MVD) . The vascular endothelial growth factor ( VEGF) levels of plasma and tumor tissue were measured by ELISA method. Results No significant difference was observed on body weight and lung metastasis rate among 3 groups ( P>0. 05) . Compared with control group, there were higher tumor inhibition rate, and lower tumor volume, MVD and VEGF levels of plasma and tumor tissue in both Avastin-L group and Avastin-H group (P<0. 05).The improvement effect of the above indexes were stronger in Avastin-H group versus Avastin-L group ( P<0. 05) . Conclusion Avastin can inhibit the growth and angiogenesis of human osteosarcoma, and reduce the VEGF level without influences on lung metastasis.