...
首页> 外文期刊>Drug Design, Development and Therapy >Tumor-induced VEGF-C overexpression in retroperitoneal lymph nodes in VX2 carcinoma-bearing rabbits
【24h】

Tumor-induced VEGF-C overexpression in retroperitoneal lymph nodes in VX2 carcinoma-bearing rabbits

机译:VX2荷瘤兔腹膜后淋巴结中肿瘤诱导的VEGF-C过表达

获取原文
           

摘要

Objective: To establish the retroperitoneal lymph node (RLN) metastasis model of cervical carcinoma in rabbits and evaluate the relationship of vascular endothelial growth factor-C (VEGF-C) expression and the lymph node status. Methods: Forty-eight rabbits were injected with VX2 cells or RPMI solution at muscular mucosae of the myometrium 0.5 cm away from the cervix. Animals were treated with or without cis-diamminedichloroplatinum(II) (cisplatin: DDP) and sacrificed on days 15, 21, and 27 post-VX2 or RPMI injections. Tumor mass and RLNs were examined histopathologically. Quantitative real-time PCR was used to examine the changes in VEGF-C mRNA expression. Levels of VEGF-C protein expression in tissues were determined using immunohistochemistry staining. Results: Development of VX2 cervical carcinoma and the RLNs metastasis was confirmed with pathological examination. Significantly increased tumor volume was observed on days 15, 21, and 27 postinjection ( P <0.05). The enlargement of RLNs was found on day 21. Expression of VEGF-C was significantly upregulated in peripheral white blood cells, tumor mass, and RLNs in an association with cancer progression. DDP resulted in a suppression of VEGF-C expression, whereas the influences on tumor mass and lymphatic metastasis were insignificant. Conclusion: Elevated VEGF-C expressions in peripheral white blood cells and RLNs are associated with tumor progression and lymphatic metastasis. DDP treatment inhibits VEGF-C expression and fails to protect against metastatic cervical cancer.
机译:目的:建立兔宫颈癌腹膜后淋巴结转移模型,评价血管内皮生长因子-C(VEGF-C)表达与淋巴结状态的关系。方法:48只家兔在距子宫颈0.5cm的子宫肌层肌肉粘膜处注射VX2细胞或RPMI溶液。用或不用顺式二甲基二氯铂(II)(顺铂:DDP)治疗动物,并在注射VX2或RPMI后第15、21和27天处死动物。病理学检查了肿瘤块和RLN。实时定量PCR用于检查VEGF-C mRNA表达的变化。使用免疫组织化学染色确定组织中VEGF-C蛋白的表达水平。结果:经病理检查证实VX2宫颈癌的发展和RLNs的转移。注射后第15、21和27天观察到肿瘤体积显着增加(P <0.05)。在第21天发现RLN的扩大。与癌症进展相关,外周血白细胞,肿瘤块和RLN中VEGF-C的表达明显上调。 DDP抑制VEGF-C表达,而对肿瘤肿块和淋巴转移的影响不明显。结论:外周血白细胞和RLNs中VEGF-C表达升高与肿瘤进展和淋巴转移有关。 DDP治疗会抑制VEGF-C的表达,并且无法预防转移性宫颈癌。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号