Liu Dan, Tao Ze-Zhang, Xiao Bo-Kui, Chen Shi-Ming, Chi Hua-Ming
Department of Otolaryngology-Head and Neck Surgery, People's Hospital, Wuhan University, Wuhan, Hubei 430060, P. R. China.
Ai Zheng. 2006 Jan;25(1):11-6.
BACKGROUND & OBJECTIVE: RNA interference (RNAi) is triggered by the presence of double-stranded RNA (dsRNA) in the cell and results in rapid destruction and post-transcriptional gene silencing of target mRNA. The roles of RNAi in gene function and antiviral therapy have been reported, but its effect on human telomerase reverse transcriptase (hTERT) gene, which is highly expressed in laryngeal squamous cell carcinoma and other head and neck neoplasms, has seldom been reported. This study was to explore the inhibitory effect of silencing hTERT gene by short hairpin RNA (shRNA) on growth of laryngeal squamous cell carcinoma xenograft in nude mice with RNAi technique.
Plasmid pshRNA containing fluorescein gene and hTERT cDNA sequences was synthesized. Human laryngeal squamous cell carcinoma Hep-2 cells were transplanted into nude mice to establish xenograft tumors. pshRNA was transfected into the tumors. The tumor volume was observed. Fluorescence expression in the tumors was observed by laser confocal microscopy. Tumor morphology was observed with HE staining. Cell apoptosis was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay. The expression of hTERT protein in the tumors was detected by SP immunohistochemistry. The structural change of heart, liver, kidney and spleen was observed, and peripheral blood hematological and biochemical parameters were determined.
The tumor volume was significantly smaller in pshRNA group than in normal saline (NS) group and blank plasmid group (P<0.01). The inhibition rate was 76.50% in pshRNA group. After transfection of pshRNA or blank plasmid, many green fluorescent cells were observed under confocal microscope. The necrosis and apoptosis of tumor cells were found under light microscope in shRNA group. The apoptotic index of tumor cells was significantly higher in pshRNA group than in NS group and blank plasmid group [(26.47+/-4.25)% vs. (2.73+/-1.35)% and (3.40+/-1.41)%, P<0.05]. pshRNA directly down-regulated hTERT protein expression in the tumors, but did no damage to the heart, liver, kidney, spleen, and blood system of nude mice.
shRNA plasmid containing specific sequences of hTERT gene could significantly inhibit the growth of laryngeal carcinoma in nude mice, with no side effect on the heart, liver, kidney, spleen, and blood system.
RNA干扰(RNAi)由细胞内双链RNA(dsRNA)的存在所触发,可导致靶mRNA的快速降解及转录后基因沉默。RNAi在基因功能及抗病毒治疗中的作用已有报道,但其对在喉鳞状细胞癌及其他头颈部肿瘤中高表达的人端粒酶逆转录酶(hTERT)基因的影响鲜有报道。本研究旨在运用RNAi技术,探讨短发夹RNA(shRNA)沉默hTERT基因对裸鼠喉鳞状细胞癌移植瘤生长的抑制作用。
合成含荧光素基因及hTERT cDNA序列的质粒pshRNA。将人喉鳞状细胞癌Hep-2细胞接种于裸鼠,建立移植瘤模型。将pshRNA转染至瘤体内,观察肿瘤体积变化。通过激光共聚焦显微镜观察瘤体内荧光表达情况。采用苏木精-伊红(HE)染色观察肿瘤形态。运用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL法)检测细胞凋亡。采用免疫组织化学链霉菌抗生物素蛋白-过氧化物酶连接法(SP法)检测瘤体内hTERT蛋白表达。观察心、肝、肾、脾的结构变化,并测定外周血血液学及生化指标。
pshRNA组肿瘤体积明显小于生理盐水(NS)组及空白质粒组(P<0.01)。pshRNA组抑制率为76.50%。转染pshRNA或空白质粒后,共聚焦显微镜下可见许多绿色荧光细胞。shRNA组光镜下可见肿瘤细胞坏死及凋亡。pshRNA组肿瘤细胞凋亡指数显著高于NS组及空白质粒组[(26.47±4.25)%比(2.73±1.35)%和(3.40±1.41)%,P<0.05]。pshRNA可直接下调瘤体内hTERT蛋白表达,但对裸鼠的心、肝、肾、脾及血液系统无损害。
含hTERT基因特异性序列的shRNA质粒可显著抑制裸鼠喉癌生长,且对心、肝、肾、脾及血液系统无副作用。