Meng Cuicui, Chen Xiaopin, Luo Zhibin
Department of Oncology, First Affiliated Hospital, Chongqing Medical University, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2013 May;29(5):458-61.
To investigate the anti-tumor effect of celecoxib combined with tegafur gimeracil oteracil potassium on subcutaneous xenograft tumor of gastric cancer in nude mice and analyze the possible mechanism.
A xenograft tumor model of gastric cancer was established subcutaneously in nude mice. After the largest diameter of tumor reached about 5 mm, the nude mice were randomly divided into 4 groups: the control group, the celecoxib group, the tegafur gimeracil oteracil potassium group, and the combination group; the drug was administered respectively for 21 days. Thereafter, tumor tissues were collected, tumor volume was measured, and tumor inhibition rate was calculated. Apoptosis was determined by TUNEL assay and the expression levels of PCNA, Bcl-2 and caspase-3 by immunohistochemistry.
The tumor inhibition rates of the celecoxib group, the tegafur gimeracil oteracil potassium group, the combination group were 30.8%, 50.1%, 78.8%, respectively. The apoptosis index in treatment groups was higher than that in the control group (P<0.01), and the combination group was higher than single drug group (P<0.01). The expressions of PCNA, Bcl-2 in treatment groups were lower than those in the control group (P<0.01), and the combination group was lower than single drug group (P<0.05). The expression of caspase-3 in treatment groups was higher than that in the control group (P<0.05), and the combination group was higher than single drug group (P<0.01).
Both celecoxib and tegafur gimeracil oteracil potassium showed obvious anti-tumor effect, and the combination of the two acted synergistically. The possible mechanism was that they inhibited tumor growth through inhibiting proliferation and promoting apoptosis of the tumor cells.
探讨塞来昔布联合替吉奥对裸鼠胃癌皮下移植瘤的抗肿瘤作用,并分析其可能机制。
建立裸鼠胃癌皮下移植瘤模型。待肿瘤最大直径达约5 mm后,将裸鼠随机分为4组:对照组、塞来昔布组、替吉奥组和联合组;分别给药21天。此后,收集肿瘤组织,测量肿瘤体积,计算肿瘤抑制率。采用TUNEL法检测凋亡情况,免疫组化法检测PCNA、Bcl-2和caspase-3的表达水平。
塞来昔布组、替吉奥组、联合组的肿瘤抑制率分别为30.8%、50.1%、78.8%。各治疗组凋亡指数均高于对照组(P<0.01),联合组高于单药组(P<0.01)。各治疗组PCNA、Bcl-2的表达均低于对照组(P<0.01),联合组低于单药组(P<0.05)。各治疗组caspase-3的表达高于对照组(P<0.05),联合组高于单药组(P<0.01)。
塞来昔布和替吉奥均显示出明显的抗肿瘤作用,二者联合具有协同作用。其可能机制是通过抑制肿瘤细胞增殖和促进凋亡来抑制肿瘤生长。