Sun Shi-Cheng, Zhao Hu, Liu Rui, Wang Bi-Liang, Liu Yi-Qing, Zhao Yan, Shi Zhen-Duo
Department of Urology, Guanyun People's Hospital, Lianyungang, Jiangsu 222200, China.
Department of Urology, Xuzhou Central Hospital, Southeast University, Xuzhou, Jiangsu 210000, China.
Zhonghua Nan Ke Xue. 2017 Feb;23(2):120-124.
To study the expression of long noncoding RNA (lncRNA) H19 in human prostate cancer tissue and its effect on the glycometabolism and growth of human prostate cancer cells.
Realtime quantitative RTPCR (qRTPCR) was employed to detect the expression of lncRNA H19 in human prostate tissues from 20 patients with prostate cancer (10 cases of highGleason score prostate cancer [HGPC] and 10 cases of lowGleason score prostate cancer [LGPC]) and another 5 with benign prostatic hyperplasia (BPH). After transfection of H19 siRNA into the DU145 and PC3 prostate cancer cells, the growth of the cells and the H19 expression in the cells were determined by MTT and qRTPCR respectively, and the changes in the glycometabolism of the prostate cancer cells were analyzed by measuring the contents of glucose and lactate in the culture medium. Nontransfected and transfected negative vectors were used as blank and negative controls respectively.
The relative expression of H19 was significantly increased in both the HGPC and LGPC tissues (0.725±0.385 and 2.086±0.542) as compared with that in the BPH tissue (0.210±0.068) (P< 0.01), even higher in the HGPC than in the LGPC tissue (P< 0.01). After transfection of H19 siRNA, the expressions of H19 were remarkably decreased in the DU145 and PC3 prostate cancer cells in comparison with those in the blank control and negative control groups (P< 0.01), and so were the proliferation of and the glucose and lactate levels in the DU145 and PC3 cells (P< 0.01).
研究长链非编码RNA(lncRNA)H19在人前列腺癌组织中的表达及其对人前列腺癌细胞糖代谢和生长的影响。
采用实时定量逆转录聚合酶链反应(qRT-PCR)检测20例前列腺癌患者(10例高Gleason评分前列腺癌[HGPC]和10例低Gleason评分前列腺癌[LGPC])以及另外5例良性前列腺增生(BPH)患者的人前列腺组织中lncRNA H19的表达。将H19 siRNA转染到DU145和PC-3前列腺癌细胞后,分别通过MTT法和qRT-PCR法测定细胞生长情况及细胞中H19的表达,并通过检测培养基中葡萄糖和乳酸的含量分析前列腺癌细胞糖代谢的变化。未转染和转染阴性载体的细胞分别作为空白对照和阴性对照。
与BPH组织(0.210±0.068)相比,HGPC和LGPC组织中H19的相对表达均显著升高(分别为0.725±0.385和2.086±0.542)(P<0.01),且HGPC组织中的表达高于LGPC组织(P<0.01)。转染H19 siRNA后,与空白对照组和阴性对照组相比,DU145和PC-3前列腺癌细胞中H19的表达显著降低(P<0.01),DU145和PC-3细胞的增殖以及葡萄糖和乳酸水平也显著降低(P<0.01)。