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[生存素RNA干扰诱导口腔鳞状癌细胞系KB和KBv200凋亡的研究]

[Study on apoptosis of oral squamous carcinoma cell line KB and KBv200 induced by survivin RNAi].

作者信息

Yan Lin, Chen Wei-Qiang, Liang Yong-Ju, Dai Chun-Ling, Wang Xiao-Hong, Shi Zhi, Chen Li-Ming, Fu Li-Wu

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, 510060, P. R. China.

出版信息

Ai Zheng. 2006 Aug;25(8):933-40.

Abstract

BACKGROUND & OBJECTIVE: Survivin, a member of IAPs (inhibition of apoptosis proteins) family, has been revealed by many studies to inhibit the activation of caspase-3, caspase-7 and caspase-9, and thus increase the anti-apoptotic effect of cancer cells, which subsequently makes the cells to become resistant to chemotherapy in cancer treatment. Survivin is expressed in human oral squamous carcinoma cell line KB and its multiple-drug resistant (MDR) cell line KBv200. This study was to compare the apoptosis induced by silencing survivin gene between these two squamous cell lines.

METHODS

Mu6/survivin plasmid which expressed shRNA against survivin was transfected into both KB and KBv200 cells to inhibit the expression of survivin gene. Survivin mRNA and protein expression was detected by semi-quantitative RT-PCR and flow cytometry (FCM), respectively. Cell apoptotic rate was measured by flow cytometry after PI staining, and apoptotic morphology of cells was observed under a fluorescent microscope after Hoechst33258 staining. Activation of caspase-3 was measured by colorimetric assay. MTT was used to evaluate the growth inhibition of tumor cells.

RESULTS

Expression of survivin, which was higher in KBv200 at mRNA and protein level, was detected in both KB and KBv200. After 48 h transfection with mu6/survivin plasmid, the expression level of survivin mRNA in KB and KBv200 was reduced by (61.98+/-8.12)% and (59.29+/-6.32)%; and that of survivin protein was decreased by (44.25+/-5.26)% and (38.76+/-4.31)% compared with the control group. Moreover, KB and KBv200 cells exhibited typical apoptotic cell morphology by Hoechst 33258 staining. Apoptosis, which was higher in KB cells, was increased significantly at 24, 48, 72 h after the transfection of mu6/surviving in KB and KBv200 cells, and reached the peak at 48 h. Similarly, activation of caspase-3 was elevated significantly, and reached the peak at 48 h. MTT assay revealed the inhibitory rates were (33.04+/-2.16)%, (56.25+/-3.32)% and (58.26+/-5.14)% in KB cells, and (35.23+/-3.42)%, (44.90+/-4.12)% and (44.19+/-4.37)% in KBv200 cells at 24, 48, 72 h after the transfection, respectively. Growth rate was lower in KB cells at 48, 72 h after the transfection compared with KBv200 cells.

CONCLUSION

RNA interference could silence the expression of survivin, which significantly induces apoptosis not only in KB cells, but also in drug resistant KBv200 cells.

摘要

背景与目的

生存素是凋亡抑制蛋白(IAPs)家族成员,多项研究表明其可抑制半胱天冬酶-3、半胱天冬酶-7和半胱天冬酶-9的激活,从而增强癌细胞的抗凋亡作用,进而使癌细胞在癌症治疗中对化疗产生耐药性。生存素在人口腔鳞状癌细胞系KB及其多药耐药(MDR)细胞系KBv200中均有表达。本研究旨在比较沉默生存素基因诱导这两种鳞状细胞系凋亡的情况。

方法

将表达针对生存素的短发夹RNA(shRNA)的Mu6/生存素质粒转染至KB和KBv200细胞中,以抑制生存素基因的表达。分别采用半定量逆转录聚合酶链反应(RT-PCR)和流式细胞术(FCM)检测生存素mRNA和蛋白表达。经碘化丙啶(PI)染色后,采用流式细胞术检测细胞凋亡率;经Hoechst33258染色后,在荧光显微镜下观察细胞凋亡形态。采用比色法检测半胱天冬酶-3的激活情况。采用MTT法评估肿瘤细胞的生长抑制情况。

结果

在KB和KBv200细胞中均检测到生存素的表达,其在KBv200细胞中的mRNA和蛋白水平均较高。用Mu6/生存素质粒转染48小时后,KB和KBv200细胞中生存素mRNA的表达水平分别降低了(61.98±8.12)%和(59.29±6.32)%;与对照组相比,生存素蛋白水平分别降低了(44.25±5.26)%和(38.76±4.31)%。此外,经Hoechst 33258染色后,KB和KBv200细胞呈现典型的凋亡细胞形态。转染Mu6/生存素后,KB和KBv200细胞在24、48、72小时的凋亡率显著增加,其中KB细胞的凋亡率更高,并于48小时达到峰值。同样,半胱天冬酶-3的激活也显著增强,并于48小时达到峰值。MTT法检测结果显示,转染后24、48、72小时,KB细胞的抑制率分别为(33.04±2.16)%、(56.25±3.32)%和(58.26±5.14)%,KBv200细胞的抑制率分别为(35.23±3.42)%、(44.90±4.12)%和(44.19±4.37)%。转染后48、72小时,KB细胞的生长速率低于KBv200细胞。

结论

RNA干扰可沉默生存素的表达,显著诱导KB细胞及耐药KBv200细胞凋亡。

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