[Effect of androgen receptor on IgG expression, proliferation and migration of prostate cancer cells in vitro]

Nan Fang Yi Ke Da Xue Xue Bao. 2017 Mar 20;37(3):388-392. doi: 10.3969/j.issn.1673-4254.2017.03.19.
[Article in Chinese]

Abstract

Objective: To investigate the effect of androgen receptor (AR) on IgG protein expression and the proliferation and migration of prostate cancer cells.

Methods: Western blotting was used to detect the expression of AR protein and IgG in androgen-dependent prostate cancer LNCap cells and castration-resistant prostate cancer PC-3 cells. In AR-overexpressing cells (PC-3-AR cells) established by transfecting PC-3 with AR gene (pCDNA3.1) and LNCap cells with small interfering RNA-mediated AR silencing (LNCap-siAR cells) were analyzed for expressions of AR protein and IgG with Western blotting; the expression of IgG mRNA was detected by Q-PCR, and the cell proliferation and migration were assessed with MTT assay and wound healing assay, respectively.

Results: Compared with PC-3 cells, LNCap cells expressed a higher level of AR protein and a lower level of IgG (P<0.05). PC-3-AR cells showed attenuated proliferation and migration with a lowered expression of IgG (P<0.01), while LNCap-siAR cells showed enhanced proliferation and migration with increased expression of IgG (P<0.01).

Conclusion: The expression of AR is inversely correlated with IgG and is associated with the proliferation and migration of prostate cancer cells in vitro.

目的: 研究前列腺癌细胞中雄激素受体(AR)对免疫球蛋白IgG表达的影响,及对前列腺癌细胞增殖、迁移的作用。

方法: (1)Western blot检测雄激素依赖性前列腺癌细胞株LNCap与去势抵抗性前列腺癌细胞株PC-3中AR、IgG蛋白的表达;(2)AR基因(pCDNA3.1+)转染PC-3构建AR过表达的PC-3-AR细胞,沉默LNCap中AR基因表达构建LNCap-siAR细胞;Western blot检测AR及IgG表达量;Q-PCR检测细胞株中IgG mRNA表达量;四氮甲基唑氮、细胞划痕方法检测细胞的增殖及迁移能力。

结果: LNCap细胞与PC-3细胞相比较,AR高表达,IgG低表达(P<0.05)。PC-3-AR细胞IgG降低表达(P<0.01),细胞增殖及迁移能力减弱;LNCap-siAR细胞IgG增高表达(P<0.01),细胞增殖及迁移能力增强。

结论: AR调控IgG蛋白表达呈负相关并与前列腺癌细胞增殖、迁移能力相关。

MeSH terms

  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation*
  • Humans
  • Immunoglobulin G / metabolism*
  • Male
  • Prostatic Neoplasms / pathology*
  • Receptors, Androgen / metabolism*

Substances

  • Immunoglobulin G
  • Receptors, Androgen

Grants and funding

广东省自然科学基金(S2013010014644)