Gao Li-fang, Wen Lian-ji, Yu Hao, Zhang Ling, Meng Yan, Shao Yue-ting, Xu De-qi, Zhao Xue-jian
Department of Pathophysiology, Basic School of Medicine, Jilin University, Changchun 130021, China.
Acta Pharmacol Sin. 2006 Mar;27(3):347-52. doi: 10.1111/j.1745-7254.2006.00277.x.
To study the effect of pSilencer1.0-U6-siRNA-stat3 on the growth of human laryngeal tumors in nude mice.
Hep2 cells were transplanted into nude mice, then at the time of tumor formation, growth rates were observed. After the tumor formed, pSilencer1.0-U6-siRNA-stat3 was injected. Tumor volumes were calculated, and growth curves were plotted. Representative histological sections were taken from mice bearing transplantation tumors in both treated and control groups, and stat3, pTyr-stat3, Bcl-2, cyclin D1, and survivin expression were detected by Western blotting. survivin mRNA levels were detected by Northern blotting, hematoxylin and eosin staining and terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick end-labeling (TUNEL) assay to confirm the apoptosis of tumors.
In nude mice, pSilencer1.0-U6-siRNA-stat3 significantly suppressed the growth of tumors compared with controls (P<0.01). It suppressed stat3 expression, and downregulated BcL2, cyclin D1, and survivin expression within the tumor. This significantly induced apoptosis of the tumors.
pSilencer1.0-U6-siRNA-stat3 was able to inhibit the growth of transplanted human laryngeal tumors in nude mice and induce apoptosis.
研究pSilencer1.0-U6-siRNA-stat3对裸鼠人喉肿瘤生长的影响。
将Hep2细胞移植到裸鼠体内,待肿瘤形成时,观察其生长速率。肿瘤形成后,注射pSilencer1.0-U6-siRNA-stat3。计算肿瘤体积并绘制生长曲线。取治疗组和对照组移植瘤小鼠的代表性组织切片,通过蛋白质免疫印迹法检测stat3、磷酸化酪氨酸-stat3、Bcl-2、细胞周期蛋白D1和生存素的表达。通过Northern印迹法检测生存素mRNA水平,苏木精-伊红染色和末端脱氧核苷酸转移酶介导的dUTP-地高辛缺口末端标记(TUNEL)法来确认肿瘤细胞凋亡。
在裸鼠中,与对照组相比,pSilencer1.0-U6-siRNA-stat3显著抑制肿瘤生长(P<0.01)。它抑制stat3表达,并下调肿瘤内BcL2、细胞周期蛋白D1和生存素的表达。这显著诱导了肿瘤细胞凋亡。
pSilencer1.0-U6-siRNA-stat3能够抑制裸鼠体内移植的人喉肿瘤生长并诱导凋亡。