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LHRH 拮抗剂西曲瑞克对上皮(BPH-1)和基质(WPMY-1)前列腺细胞交迭条件培养基的影响。

The effect of LHRH antagonist cetrorelix in crossover conditioned media from epithelial (BPH-1) and stromal (WPMY-1) prostate cells.

机构信息

Veterans Affairs Medical Center, Miami, FL, USA.

出版信息

Horm Metab Res. 2014 Jan;46(1):21-6. doi: 10.1055/s-0033-1349127. Epub 2013 Jul 9.

Abstract

Stromal cells strictly modulate the differentiation of the normal prostate epithelium. In benign prostatic hyperplasia (BPH) tissue, the ratio of stromal to epithelial cells reaches a 5:1 ratio. In this study, we evaluated the effects of crossover conditioned media (CM) of stromal and epithelial prostate cells before and after treatment with LHRH antagonist Cetrorelix. WPMY-1 human prostate stromal cells and BPH-1 human benign prostatic hyperplasia cells were cultured in vitro and the effects of crossover conditioned media (CM) from those cells were studied. We evaluated the effect of Cetrorelix on the expression of PCNA and p53 in those cells. We then studied the effect of Cetrorelix on BPH-1 cells cultured with the CM from WPMY-1 cells, as well as the mechanisms which govern these interactions. CM from WPMY-1 cells strongly stimulated the proliferation of BPH-1 cells in a dose dependent manner, while CM from BPH-1 cells only slightly increased the proliferation of WPMY-1 cells. Cetrorelix inhibited the proliferation of both cell lines and the expression of PCNA, while the expression of p53 was increased. Cetrorelix also inhibited the proliferation of BPH-1 cells stimulated with the CM from WPMY-1 cells. In the crossover experiment, conditioned media from WPMY-1 and BPH-1 cells increased the expression of phosphorylated ERK1/2 and STAT3. Our results support previous observations on the bidirectional stromal-epithelial interactions in prostate gland and shed more light on the mechanistic action of those effects. Our study strongly supports the hypothesis that LHRH antagonists may be beneficial for BPH prevention and treatment.

摘要

基质细胞严格调节正常前列腺上皮细胞的分化。在良性前列腺增生 (BPH) 组织中,基质细胞与上皮细胞的比例达到 5:1。在这项研究中,我们评估了 LHRH 拮抗剂 Cetrorelix 治疗前后前列腺基质和上皮细胞交叉条件培养基 (CM) 的作用。体外培养 WPMY-1 人前列腺基质细胞和 BPH-1 人良性前列腺增生细胞,并研究这些细胞的交叉条件培养基 (CM) 的作用。我们评估了 Cetrorelix 对这些细胞中 PCNA 和 p53 表达的影响。然后,我们研究了 Cetrorelix 对用 WPMY-1 细胞 CM 培养的 BPH-1 细胞的作用,以及控制这些相互作用的机制。WPMY-1 细胞的 CM 强烈地以剂量依赖的方式刺激 BPH-1 细胞的增殖,而 BPH-1 细胞的 CM 仅轻微地增加 WPMY-1 细胞的增殖。Cetrorelix 抑制了两种细胞系的增殖和 PCNA 的表达,而 p53 的表达增加。Cetrorelix 还抑制了用 WPMY-1 细胞 CM 刺激的 BPH-1 细胞的增殖。在交叉实验中,来自 WPMY-1 和 BPH-1 细胞的条件培养基增加了磷酸化 ERK1/2 和 STAT3 的表达。我们的结果支持了先前关于前列腺中双向基质-上皮相互作用的观察结果,并进一步阐明了这些作用的机制作用。我们的研究强烈支持了 LHRH 拮抗剂可能有益于 BPH 的预防和治疗的假设。

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