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细胞因子IL-2和IL-6对胰腺癌细胞表达VEGF-D的调节[J]. 肿瘤防治研究, 2009, 36(08): 651-654. DOI: 10.3971/j.issn.1000-8578.2009.08.006
引用本文: 细胞因子IL-2和IL-6对胰腺癌细胞表达VEGF-D的调节[J]. 肿瘤防治研究, 2009, 36(08): 651-654. DOI: 10.3971/j.issn.1000-8578.2009.08.006
Cytokines IL-2 and IL-6 Regulate Expression of VEGF-D in Pancreatic Cancer Cells[J]. Cancer Research on Prevention and Treatment, 2009, 36(08): 651-654. DOI: 10.3971/j.issn.1000-8578.2009.08.006
Citation: Cytokines IL-2 and IL-6 Regulate Expression of VEGF-D in Pancreatic Cancer Cells[J]. Cancer Research on Prevention and Treatment, 2009, 36(08): 651-654. DOI: 10.3971/j.issn.1000-8578.2009.08.006

细胞因子IL-2和IL-6对胰腺癌细胞表达VEGF-D的调节

Cytokines IL-2 and IL-6 Regulate Expression of VEGF-D in Pancreatic Cancer Cells

  • 摘要: 目的 探讨细胞因子白细胞介素2(IL-2)和白细胞介素6(IL-6)对胰腺癌细胞表达VEGF-D的调节。 方法 以细胞因子IL-2或IL-6分别刺激胰腺癌细胞株SW1990和BXPC-3后用逆转录-聚合酶链式反应技术(RT-PCR)分析其VEGF-D 基因的表达。 结果 IL-2使细胞株SW1990和BXPC-3产生VEGF-D mRNA减少;IL-6使细胞株SW1990产生VEGF-D mRNA增加,但对细胞株BXPC-3产生VEGF-D mRNA无明显影响。 结论 IL-2抑制胰腺癌细胞VEGF-D mRNA的表达,从而抑制胰腺癌淋巴结转移;IL-6促进某些胰腺癌细胞VEGF-D mRNA的表达,但对胰腺癌细胞生物学特性的影响有待于进一步深入研究。

     

    Abstract: Objective To explore the function of cytokines interleukin-2(IL-2) and interleukin-6 (IL-6) on regulating the expression of vascular endothelial growth factor D(VEGF-D) in cultured human pancreatic cancer cell lines. Methods We used reverse transcription polymerase chain reaction(RT-PCR) methods to anaylyze VEGF-D mRNA level in two cultured human pancreatic cancer cell lines(SW1990 and BXPC-3) under the stimulation with IL-2 or IL-6. Results RT-PCR analysis revealed the expression of VEGF-D gene was decreased in SW1990 cell or BXPC-3 cell stimulated by IL-2. IL-6 up-regulated VEGF-D mRNA of SW1990 cell,the in consistency-dependent, but there was no effect on VEGF-D mRNA expression of BXPC-3 cell line. Conclusion IL-2 inhibits lymph node metastasis of pancreatic cancer by inhibiting expression of VEGF-D; IL-6 increases expression of VEGF-D mRNA in several pancreatic cancer cell, but the effects on biological characteristic of pancreatic cancer cell still need to be continuing studied.

     

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