中国癌症杂志 ›› 2013, Vol. 23 ›› Issue (4): 248-253.doi: 10.3969/j.issn.1007-3969.2013.04.002

• 论著 • 上一篇    下一篇

白介素8的3种亚型对卵巢癌SKOV3细胞生物学活性的影响

王爱萍,王琪,张玮,尹巧云,李力   

  1. 广西医科大学肿瘤医院妇瘤科,广西区域高发肿瘤重点实验室,广西 南宁530021
  • 出版日期:2013-04-25 发布日期:2014-11-19
  • 通信作者: 李力 E-mail:lili@gxmu.edu.cn
  • 基金资助:
    国家自然科学基金(No:30760266)

The impact of three subtypes of IL-8 on biological functions of ovarian cancer SKOV3 cells

WANG Ai-ping, WANG Qi, ZHANG Wei, YIN Qiao-yun, LI Li   

  1. Department of Gynecology Oncology, Affiliated Tumor Hospital of Guangxi Medical University and the Emphasis Lab of High Incidence Cancer in Guangxi Region, Nanning Guangxi 530021, China
  • Published:2013-04-25 Online:2014-11-19
  • Contact: LI Li E-mail: lili@gxmu.edu.cn

摘要:

背景与目的:卵巢癌的进展是一种多因素、多环节、多阶段的过程,近来研究表明卵巢癌患者白介素8(IL-8)水平显著高于良性肿瘤患者及健康人群,卵巢癌的生长和转移可能与过度表达的IL-8有关,但尚无报道表明IL-8主要亚型在卵巢癌中的作用。本研究探讨IL-83种亚型IL-8(1-77)IL-8(5-77)IL-8(9-77)对卵巢癌SKOV3细胞的增殖、生长、迁移和侵袭能力的影响及其作用机理。方法:确认分别获得IL-83种亚型稳定转染的SKOV3细胞后,应用MTT比色测定法比较各细胞的生长曲线;采用流式细胞仪比较各细胞的细胞生长周期;采用集落形成实验比较各组细胞的克隆率;运用Transwell小室比较各细胞体外迁移和侵袭能力。结果:IL-8(1-77)-pwpi-SKOV3细胞和IL-8(5-77)-pwpi-SKOV3G2期的比率明显高于SKOV3(P=0.017P=0.020)IL-8(1-77)-pwpi-SKOV3IL-8(5-77)-pwpi-SKOV3细胞克隆率明显高于SKOV3(P=0.000P=0.001)IL-8(9-77)-pwpi-SKOV3细胞克隆率明显低于SKOV3(P=0.013);细胞体外迁移能力多组间差异无统计学意义(P>0.05),但细胞体外侵袭能力IL-8(1-77)-pwpi-SKOV3IL-8(5-77)-pwpi-SKOV3明显强于SKOV3(P=0.000P=0.002)IL-8(9-77)-pwpi-SKOV3明显弱于SKOV3(P=0.067)结论:IL-8(1-77)IL-8(5-77)可能促进卵巢癌SKOV3细胞的生长和增殖,并增强其侵袭能力,而IL-8(9-77)对卵巢癌SKOV3细胞增殖可能有抑制作用。

关键词: 卵巢上皮癌, IL-8亚型, 生物学功能

Abstract:

Background and purpose: Ovarian cancer progression is a multistep process. Recent research shows that IL-8 level of ovarian cancer patients is significantly higher than that of patients with benign tumors and normal people, the growth and metastasis of ovarian cancer may be associated with over-expression of IL-8, but there is no report about the function of the main subtypes of IL-8 in ovarian cancer. The study was to investigate the influence of IL-8 three subtypes on ovarian cancer SKOV3 cell proliferation, growth, migrating and invasive capability, and the underlying mechanism. Methods: After confirming obtaining SKOV3 cell with three hypotypes IL-8(1-77), IL-8(5-77), IL-8(9-77) over-expression respectively, MTT colorimetric method was used to detect the growth cure of different cells; The flow cytometry was used to compare the cell cycle of different cells; The cell proliferation capability of different cells was tested by the cell body colony formation; Transwell closet was used to compare different cell body’s external migration and invasive capability. Results: IL-8(1-77)-pwpi-SKOV3 and IL-8(5-77)-pwpi-SKOV3 cells in the ratio of G2 phase were significantly higher than that of SKOV3 cells (P=0.017 and 0.020). The cloning formation rate of IL-8(1-77)-pwpi-SKOV3 and IL-8 (5-77) -pwpi-SKOV3 cells were significantly higher than that of SKOV3 cells (P=0.000 and 0.001), IL-8 (9-77)-pwpi-SKOV3 cells was significantly lower than SKOV3 cells (P=0.013); the migration ability in vitro of different groups of cells had no statistically significant differences (P>0.05), but the invasion ability in vitro of IL-8( 1-77 )-pwpi-SKOV3 and IL-8 (5-77) -pwpi-SKOV3 cells were significantly stronger than that of SKOV3 cells(P=0.000 and 0.002), IL-8 (9-77) -pwpi-SKOV3 cells was significantly weaker than that of SKOV3 cells(P=0.067). Conclusion: The subtypes of IL-8 (1-77) and IL-8 (5-77) can promote ovarian cancer SKOV3 cell growth and proliferation, and enhance their invasive ability, while IL-8(9-77) inhibits proliferation of ovarian cancer SKOV3 cells.

Key words: Ovarian cancer, IL-8 subtype, Biological functions