龙欣欣①, 叶英楠②, 刘芃芃②, 张丽杰①, 于文文①, 魏枫①, 于津浦①②. 神经降压素对肝细胞肝癌生长和侵袭的影响*[J]. 中国肿瘤临床, 2016, 43(7): 275-280. DOI: 10.3969/j.issn.1000-8179.2016.07.249
引用本文: 龙欣欣①, 叶英楠②, 刘芃芃②, 张丽杰①, 于文文①, 魏枫①, 于津浦①②. 神经降压素对肝细胞肝癌生长和侵袭的影响*[J]. 中国肿瘤临床, 2016, 43(7): 275-280. DOI: 10.3969/j.issn.1000-8179.2016.07.249
Xinxin LONG1, Yingnan YE2, Pengpeng LIU2, Lijie ZHANG1, Wenwen YU1, Feng WEI1, Jinpu YU1. Effects of neurotensin on the growth and invasion of hepatocellular carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(7): 275-280. DOI: 10.3969/j.issn.1000-8179.2016.07.249
Citation: Xinxin LONG1, Yingnan YE2, Pengpeng LIU2, Lijie ZHANG1, Wenwen YU1, Feng WEI1, Jinpu YU1. Effects of neurotensin on the growth and invasion of hepatocellular carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(7): 275-280. DOI: 10.3969/j.issn.1000-8179.2016.07.249

神经降压素对肝细胞肝癌生长和侵袭的影响*

Effects of neurotensin on the growth and invasion of hepatocellular carcinoma

  • 摘要: 目的:探讨神经降压素(neurotensin ,NTS)与肝细胞肝癌(hepatocellular carcinoma ,HCC )生长和侵袭性的关系。方法:随机选取天津医科大学肿瘤医院100 例经部分肝切除术治疗的HCC 患者的临床病理资料,并分析NTS 、神经降压素受体1(neurotensin receptor 1,NTR 1)与临床病理指标的相关性。以Hep3B 细胞为基础,通过基因转染技术和RNA 干扰技术构建不同NTR 1 表达水平的HCC 细胞系。利用BrdU增殖实验、AnnexinV凋亡实验、划痕修复实验、Transwell 侵袭实验来观察不同NTS 处理和不同NTR 1表达水平的细胞在增殖、凋亡、迁移、侵袭上的差异。结果:NTS 、NTR 1 表达与HCC 患者包膜完整性和门静脉癌栓浸润等转移指标密切相关。外源性NTS 刺激和高表达NTR 1 对Hep3B 细胞的增殖与凋亡无影响。Hep3BNTR 1hi细胞的划痕修复率和侵袭细胞数均显著高于Hep3Bwt细胞,Hep3BNTR 1-细胞的划痕修复率和侵袭细胞数均显著低于Hep3Bwt细胞,同样NTS 处理的Hep3Bwt、Hep3BN TR1hi细胞的划痕修复率和侵袭细胞数均高于对照组。结论:HCC 组织中NTS 、NTR 1 高表达与肝癌高侵袭性相关,外源性NTS 刺激和高表达NTR 1 不影响HCC 的增殖凋亡,但会增强其侵袭性。

     

    Abstract: Objective:To study the effects of neurotensin (NTS) on the growth and invasion of hepatocellular carcinoma (HCC). Meth-ods: The clinicopathological characteristics of 100 patients with HCC were analyzed. The correlations between NTS and neurotensin re-ceptor 1 (NTR 1) expression and clinicopathological parameters were identified. Hep 3B hepatoma cells with different levels of NTR 1 were established via gene transfection and siRNA interference. BrdU proliferation assay, Annexin V apoptosis assay, scratch repair ex-periments, and Transwell invasion assay were used to compare the functional alterations of hepatoma cells upon different NTS stimula-tion. Results:NTS/NTR 1 expression in tissues was significantly correlated with incomplete envelope and portal vein invasion of HCC pa -tients. Exogenous NTS stimulation and NTR 1 over-expression do not affect proliferation and apoptosis of HCC cell lines. The wound clo-sure rate and invasion cell number of Hep 3B NTR 1hi were significantly higher than those of Hep 3Bwt; in addition, the wound closure rate and invasion cell number of Hep3B NTR 1-are lower than those of Hep3B wt. In parallel, NTS-treated Hep 3Bwt and Hep3B NTR 1hi cells have high -er wound closure rates and invasion cell number than NTS untreated cells. Conclusion: High NTS/NTR 1 expression correlated with ag-gressive phenotype of HCC. Exogenous NTS stimulation and NTR1 over-expression do not affect proliferation and apoptosis of HCC cell
    lines, but can improve invasion.

     

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