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Inhibition of growth and metastasis of human gastric cancer implanted in nude mice by d-limonene

机译:d-柠檬烯对裸鼠体内人胃癌生长和转移的抑制作用

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摘要

AIM: To investigate the effects and mechanism of d-limonene on the growth and metastasis of gastric cancer in vivo.METHODS: Metastatic model simulating human gastric cancer was established by orthotopic implantation of histologically intact human tumor tissue into gastric wall of nude mice. One percent d-limonene was orally administered at dose of 15 ml/kg every other day for seven weeks. Eight weeks after implantation, tumor weight, inhibition rate, apoptotic index (AI), microvessel density (MVD), vascular endothelial growth factor (VEGF), variation of ultrastructure, and the presence of metastasis were evaluated, respectively, after the mice were sacrificed.RESULTS: The tumor weight was significantly reduced in 5-FU group (2.55 ± 0.28 g), d-limonene group (1.49 ± 0.09 g) and combined treatment group (1.48 ± 0.21 g) compared with the control group(2.73 ± 0.23 g, P < 0.05). In 5-FU group, d-limonene group, combined treatment group, the inhibition rates were 2.60%, 47.58% and 46.84% and 0, respectively; AI was (3.31 ± 0.33)%, (8.26 ± 1.21)%, (20.99 ± 1.84)% and (19.34 ± 2.19)%, respectively; MVD was (8.64 ± 2.81), (16.77 ± 1.39), (5.32 ± 4.26) and (5.86 ± 2.27), respectively; VEGF expression was (45.77 ± 4.79), (41.34 ± 5.41), (29.71 ± 8.92) and (28.24 ± 8.55), respectively. The incidences of peritoneal metastasis also decreased significantly in 5-FU group(77.8%), d-limonene group (20.0%) and combined group (22.2%) compared with control group (100%) versus 62.5%, 30% and 22.2%) (P < 0.05). Liver metastasis was also inhibited and the incidences decreased significantly in 5-FU group, d-limonene group and combined group than that in control group (87.5% vs 55.5%, 20.0% and 22.2% respectively) (P < 0.05). The incidence of ascites in control group, 5-FU group, d-limonene group and combined group was 25.0%, 22.2%, 0, 0, respectively and 12.5%, 11.1% 0, 0, with respect to the metastasis rate to other organs.CONCLUSION: d-limonene has antiangiogenic and proapoptotic effects on gastric cancer, thereby inhibits tumor growth and metastasis. Combination of d-limonene with cytotoxic agents may be more effective.
机译:目的:探讨d-柠檬烯在体内对胃癌生长和转移的影响及其机制。方法:通过将组织完整的人肿瘤组织原位植入裸鼠胃壁,建立模拟人胃癌的转移模型。每隔一天以15 ml / kg的剂量口服7%的d-柠檬烯。植入后八周,处死小鼠后分​​别评估肿瘤重量,抑制率,凋亡指数(AI),微血管密度(MVD),血管内皮生长因子(VEGF),超微结构变化和转移的存在。结果:5-FU组(2.55±0.28 g),d-柠檬烯组(1.49±0.09 g)和联合治疗组(1.48±0.21 g)与对照组(2.73±0.23)相比,肿瘤重量显着降低g,P <0.05)。 5-FU组,d-柠檬烯组,联合治疗组的抑制率分别为2.60%,47.58%和46.84%和0。 AI分别为(3.31±0.33)%,(8.26±1.21)%,(20.99±1.84)%和(19.34±2.19)%; MVD分别为(8.64±2.81),(16.77±1.39),(5.32±4.26)和(5.86±2.27); VEGF表达分别为(45.77±4.79),(41.34±5.41),(29.71±8.92)和(28.24±8.55)。 5-FU组(77.8%),d-柠檬烯组(20.0%)和联合组(22.2%)的腹膜转移发生率也比对照组(100%)显着降低,分别为62.5%,30%和22.2% )(P <0.05)。 5-FU组,d-柠檬烯组和联合组的肝转移也得到了抑制,其发生率显着低于对照组(分别为87.5%,55.5%,20.0%和22.2%)(P <0.05)。相对于其他部位的转移率,对照组,5-FU组,d-柠檬烯组和联合组的腹水发生率分别为25.0%,22.2%,0、0和12.5%,11.1%0、0。结论:d-柠檬烯对胃癌具有抗血管生成和促凋亡作用,从而抑制肿瘤的生长和转移。 d-柠檬烯与细胞毒剂联合使用可能更有效。

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