Gao Zhi-qiang, Han Bao-hui, Sha Hui-fang, Shi Zhen-yu, Yang Xiao-hua, Feng Jiu-xian
Department of Pulmonary Medicine, Chest Hospital Affiliated to Shanghai Jiaotong University, Shanghai 200030, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2010 Apr;33(4):284-8.
To study the effects and possible mechanisms of the protein kinase C (PKC) inhibitor chelerythrine chloride (CH), combined with cisplatin (DDP) on human non-small cell lung cancer.
The effect of CH, DDP and the combination on proliferation and apoptosis of human lung cancer cell line A549 were evaluated by MTT assay and flow cytometry respectively. The inhibitory effects of CH and DDP on neoplasia were verified on subcutaneous implanted tumor of nude mice. Implanted tumor models were constructed in nude mice using human lung adenocarcinoma cell line A549. Twenty-four BALB/c nude mice with implanted tumors were divided into 4 groups randomly: group CH, group DDP, group CH + DDP, and normal saline group (group NS), each with 5 mice. CH, DDP or NS were intraperitoneally injected into nude mice for 3 weeks (DDP or NS was injected once a week, CH was injected twice a week).
CH inhibited A549 cell proliferation in a concentration-dependent pattern. When CH and DDP were combined, the inhibitory effect was enhanced in a synergistic or additive pattern. Both CH and DDP significantly increased the apoptosis of A549 cells, and this action was remarkably increased when DDP was combined with CH. CH and DDP inhibited the growth of subcutaneous implanted tumor in nude mice and the inhibitory rate of group CH + DDP (80.5%) was significantly higher than that of group CH (72.4%) or group DDP (64.3%) (t = 11.34, P < 0.01).
CH combined with DDP shows significantly synergistic anti-tumor effects on non-small cell lung cancer cell line A549 and subcutaneous implanted tumor in nude mice, possibly by enhancement of growth inhibition and apoptosis induction on tumor cells.
研究蛋白激酶C(PKC)抑制剂氯化白屈菜红碱(CH)联合顺铂(DDP)对人非小细胞肺癌的作用及其可能机制。
分别采用MTT法和流式细胞术评估CH、DDP及其联合应用对人肺癌细胞系A549增殖和凋亡的影响。通过裸鼠皮下移植瘤验证CH和DDP对肿瘤形成的抑制作用。用人肺腺癌细胞系A549构建裸鼠移植瘤模型。将24只接种肿瘤的BALB/c裸鼠随机分为4组:CH组、DDP组、CH + DDP组和生理盐水组(NS组),每组5只。对裸鼠腹腔注射CH、DDP或NS,共3周(DDP或NS每周注射1次,CH每周注射2次)。
CH以浓度依赖性方式抑制A549细胞增殖。CH与DDP联合应用时,抑制作用呈协同或相加增强。CH和DDP均显著增加A549细胞凋亡,DDP与CH联合时该作用明显增强。CH和DDP抑制裸鼠皮下移植瘤生长,CH + DDP组的抑制率(80.5%)显著高于CH组(72.4%)或DDP组(64.3%)(t = 11.34,P < 0.01)。
CH联合DDP对人非小细胞肺癌细胞系A549及裸鼠皮下移植瘤具有显著的协同抗肿瘤作用,可能是通过增强对肿瘤细胞的生长抑制和凋亡诱导作用实现的。