临床泌尿外科杂志
臨床泌尿外科雜誌
림상비뇨외과잡지
JOURNAL OF CLINICAL UROLOGY
2009年
7期
542-545
,共4页
曾四平%肖亚军%章小平%杨军%李炎生%钱晓辉%许易%吕吉宁
曾四平%肖亞軍%章小平%楊軍%李炎生%錢曉輝%許易%呂吉寧
증사평%초아군%장소평%양군%리염생%전효휘%허역%려길저
肾细胞癌%肺转移%动物模型%MicroRNAs
腎細胞癌%肺轉移%動物模型%MicroRNAs
신세포암%폐전이%동물모형%MicroRNAs
renal cell carcinoma%pulmonary metastasis%animal model%miroRNAs
目的:建立人肾细胞癌原位移植裸鼠肺转移动物模型,研究Has-mir-129对肾脏移植瘤和肺部转移瘤的影响.方法:构建Has-mir-129慢病毒载体,以人肾癌细胞株SN12-PM6建立的动物模型作为对照组,以Has-mir-129慢病毒载体感染肾癌细胞建立的动物模型作为实验组;7周后观察裸鼠肾脏肿瘤及肺部转移瘤的生长情况,并分别计算两组的肾脏成瘤率、肺部转移率及肿瘤的重量;所有标本均采用10%甲醛溶液固定,常规石蜡包埋、切片、HE染色后分析结果.结果:对照组肾脏成瘤率为100%(8/8),肺部转移率为100%(8/8),肿瘤重量平均为(0.712 8±0.147 4)g;实验组肾脏成瘤率为100%(8/8),肺部转移率为62.5%(5/8),肿瘤重量平均为(0.481 5±0.111 2)g;肾脏成瘤率两者之间差异无统计学意义,肿瘤重量和肺部转移率差异有统计学意义(P<0.05).结论:成功建立了Has-mir-129慢病毒载体及人肾细胞癌原位移植裸鼠肺转移动物模型.发现Has-mir-129能抑制人肾细胞癌原位移植裸鼠肺转移模型移植瘤的生长及肺部转移瘤的形成.
目的:建立人腎細胞癌原位移植裸鼠肺轉移動物模型,研究Has-mir-129對腎髒移植瘤和肺部轉移瘤的影響.方法:構建Has-mir-129慢病毒載體,以人腎癌細胞株SN12-PM6建立的動物模型作為對照組,以Has-mir-129慢病毒載體感染腎癌細胞建立的動物模型作為實驗組;7週後觀察裸鼠腎髒腫瘤及肺部轉移瘤的生長情況,併分彆計算兩組的腎髒成瘤率、肺部轉移率及腫瘤的重量;所有標本均採用10%甲醛溶液固定,常規石蠟包埋、切片、HE染色後分析結果.結果:對照組腎髒成瘤率為100%(8/8),肺部轉移率為100%(8/8),腫瘤重量平均為(0.712 8±0.147 4)g;實驗組腎髒成瘤率為100%(8/8),肺部轉移率為62.5%(5/8),腫瘤重量平均為(0.481 5±0.111 2)g;腎髒成瘤率兩者之間差異無統計學意義,腫瘤重量和肺部轉移率差異有統計學意義(P<0.05).結論:成功建立瞭Has-mir-129慢病毒載體及人腎細胞癌原位移植裸鼠肺轉移動物模型.髮現Has-mir-129能抑製人腎細胞癌原位移植裸鼠肺轉移模型移植瘤的生長及肺部轉移瘤的形成.
목적:건립인신세포암원위이식라서폐전이동물모형,연구Has-mir-129대신장이식류화폐부전이류적영향.방법:구건Has-mir-129만병독재체,이인신암세포주SN12-PM6건립적동물모형작위대조조,이Has-mir-129만병독재체감염신암세포건립적동물모형작위실험조;7주후관찰라서신장종류급폐부전이류적생장정황,병분별계산량조적신장성류솔、폐부전이솔급종류적중량;소유표본균채용10%갑철용액고정,상규석사포매、절편、HE염색후분석결과.결과:대조조신장성류솔위100%(8/8),폐부전이솔위100%(8/8),종류중량평균위(0.712 8±0.147 4)g;실험조신장성류솔위100%(8/8),폐부전이솔위62.5%(5/8),종류중량평균위(0.481 5±0.111 2)g;신장성류솔량자지간차이무통계학의의,종류중량화폐부전이솔차이유통계학의의(P<0.05).결론:성공건립료Has-mir-129만병독재체급인신세포암원위이식라서폐전이동물모형.발현Has-mir-129능억제인신세포암원위이식라서폐전이모형이식류적생장급폐부전이류적형성.
Objective:To construct orthotopic mouse model of human renal cell carcinoma with pulmonary me-tastasis and to study the impact of miRNA-129 on renal transplantation tumor and lung metastases. Methods: We constructed the lent;viral vector of has-mir-129 and set up the animal model of human renal cancer cell line SN12-PM6 being infected with the lent;viral vector as the experiment group. And we set up the animal model of human renal cancer cell line SN12-PM6 as the control group. After 7 weeks tumorigenicity and metastasis were evaluated subsequently. In the two groups, the percentage of tumorigenicity and metastasis was calculated; at the same time, the weight of tumor was also measured. All tumor tissues were fixed in 10% formalin and embedded in par-affin routinely. Paraffin-embedded tissues were sectioned and stained with hematoxylin and eosin (HE) for routine histological examination. Results: In the control group, the percentage of tumorigenicity was 100% (8/8), the per-centage of metastasis was 100%(8/8) and the average tumor weight was(0.712 8±0.147 4)g. But in the experi-ment group, the percentage of tumorigenicity was 100 % (8/8), the percentage of metastasis was 62.5%(5/8) and the average tumor weight was(0.481 5±0.111 2)g. Statistics show that the percentage of tumorigenicity was not significant different between the two groups, but the average tumor weight and the percentage of metastasis was significantly different between the two groups(P<0.05). Conclusions: We have successfully constructed has-mir-129 Impacted orthotopic mouse model of human renal cell carcinoma with pulmonary metastasis. Has-mir-129 can inhibit tumor growth and pulmonary metastasis of orthotopic mouse model of human renal cell carcinoma with pulmonary metastasis.