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Different expression of androgen receptor coactivators in human prostate.

机译:雄激素受体共激活剂在人前列腺中的不同表达。

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OBJECTIVES: To investigate the expression of androgen receptor (AR) coactivators in the human prostate for a better understanding of androgen action in prostate cancer. METHODS: Using reverse transcriptase-polymerase chain reaction, we examined the expression levels of AR coactivators (ARA55, SRC1, ARA54, TIF2, RAC3) in four prostate cancer cell lines (DU145, PC3, LNCaP, and LN-TR2), nine benign prostatic tissue samples, and 21 prostate cancer tissue specimens. RESULTS: In the cell lines, SRC1 was expressed ubiquitously at almost equal amounts. Contrary to this, ARA55, ARA54, TIF2, and RAC3 displayed cell line-specific expression. In the LN-TR2 cells, established from LNCaP cells by long-term treatment with tumor necrosis factor-alpha, the expression levels of ARA55 and TIF2 were much higher than those in the LNCaP cells. In every prostatic tissue specimen, the expression levels of TIF2 and RAC3 were very low. The expression levels of ARA55 and SRC1 were higher in the cancer specimens with a higher grade or poor response to endocrine therapy than in those with a lower grade or good response to endocrine therapy. CONCLUSIONS: Prostate cancer cells express AR coactivators. Long-term stimulation by tumor necrosis factor-alpha could increase ARA55 and TIF2 expression in LNCaP cells. The different expression of coactivators may contribute to the different response of prostate cancer to androgenic stimulation or endocrine therapy.
机译:目的:研究雄激素受体(AR)共激活因子在人前列腺中的表达,以更好地了解前列腺癌中雄激素的作用。方法:使用逆转录酶-聚合酶链反应,我们检测了AR共激活因子(ARA55,SRC1,ARA54,TIF2,RAC3)在四种前列腺癌细胞系(DU145,PC3,LNCaP和LN-TR2)中的表达水平,其中九种是良性的前列腺组织样本和21个前列腺癌组织样本。结果:在细胞系中,SRC1以几乎相等的量无处不在地表达。与此相反,ARA55,ARA54,TIF2和RAC3显示了细胞系特异性表达。在通过长期用肿瘤坏死因子α治疗从LNCaP细胞建立的LN-TR2细胞中,ARA55和TIF2的表达水平远高于LNCaP细胞中的表达水平。在每个前列腺组织标本中,TIF2和RAC3的表达水平都非常低。在对内分泌治疗有较高等级或反应较差的癌症标本中,ARA55和SRC1的表达水平要比对内分泌治疗较低或较高等级的癌标本中的高。结论:前列腺癌细胞表达AR共激活因子。肿瘤坏死因子-α的长期刺激可增加LNCaP细胞中ARA55和TIF2的表达。共激活因子的不同表达可能有助于前列腺癌对雄激素刺激或内分泌治疗的不同反应。

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